pyrazines has been researched along with Breast Cancer in 114 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (0.88) | 18.2507 |
2000's | 37 (32.46) | 29.6817 |
2010's | 69 (60.53) | 24.3611 |
2020's | 7 (6.14) | 2.80 |
Authors | Studies |
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Feng, Y; Fu, X; Li, Z; Lin, F; Lv, J; Mao, Q; Mou, Y; Wang, S; Yang, Y; Zhang, B; Zhang, L; Zhang, P; Zhao, J | 1 |
Kumar, J; Kusanur, R; Niranjan, V; Philip, S; R, V; Uttarkar, A | 1 |
Chen, H; Fang, J; Jiang, S; Ruan, Q; Sun, J; Yang, X; Zhang, M; Zhang, Y; Zhou, F; Zhou, W; Zhu, T | 1 |
Alexi, X; Boven, E; Kruger, DT; Linn, SC; Opdam, M; Sanders, J; Schuurman, K; van der Noort, V; Voorwerk, L; Zwart, W | 1 |
Bajzikova, M; Boukalova, S; Coelho, A; Davidova, E; Ditzel, HJ; Hubackova, S; Kovarova, J; Neuzil, J; Rohlena, J; Terp, MG | 1 |
Andrews, C; Maze, D; Murphy, T; Sibai, H | 1 |
Chen-Yang, Z; Hui, MA; Li-Chun, C; Ming-Kun, S; Qing, F; Ren Bao Li Gao, A; Xiang-Yang, L; Zhen-Long, YU | 1 |
Kim, SB; Nishihara, R; Paulmurugan, R; Suzuki, K | 1 |
Morimoto-Kamata, R; Yui, S | 1 |
Cui, G; Deng, H; Lee, SM; Lu, Y; Shan, L; Zhang, Y; Zhou, H | 1 |
Afjei, R; Citterio, D; Hiruta, Y; Iwasawa, N; Kim, SB; Nakajima, T; Natarajan, A; Nishihara, R; Nishiyama, S; Paulmurugan, R; Sato, M; Suzuki, K; Yamamoto, E | 1 |
Bruni-Cardoso, A; Fiore, APZP; Gomes, LR; Kinker, GS; Martins, DJ; Menck, CFM; Rocha, CRR | 1 |
Cabañas, C; Cardeñes, B; López-Martín, S; Morales, S; Toribio, V; Yáñez-Mó, M | 1 |
Abu-Odeh, R; Al-Qawasmeh, RA; Al-Tel, TH; Chouaib, S; El-Awady, R; Saber-Ayad, M; Semreen, MH; Voelter, W | 1 |
Altıkat, S; Boyaci, I; Cavga, FZ; Irmak, R; Kocacan, SA; Yerlikaya, A | 1 |
Che, XF; Kohno, N; Komatsu, S; Miyazawa, K; Moriya, S; Yokoyama, T | 1 |
Erdoğan, E; Genç, O; Savran, B; Yerlikaya, A | 1 |
Aoyama, K; Asano, M; Dougan, DR; Hamada, T; Hashimoto, K; Ishikawa, T; Mol, CD; Morishita, N; Saito, B; Shiokawa, Z; Sumi, H; Yabuki, M; Yoshida, S; Yoshimatsu, M | 1 |
Khan, S; Li, WH; Sun, SR; Tang, Z; Wan, JN; Wang, CH; Yao, F; Zhang, YM; Zhu, S | 1 |
Condelli, V; Esposito, F; Landriscina, M; Lettini, G; Maddalena, F; Matassa, DS; Sisinni, L | 1 |
Abramova, EB; Astakhova, TM; Bogomyagkova, YV; Choinzonov, EL; Erokhov, PA; Kondakova, IV; Kuznetsov, NA; Lyupina, YV; Plekhanova, AS; Rodoman, GV; Sharova, NP; Shashova, EE; Slonimskaya, EM; Sumedi, IR | 1 |
Iyengar, R; Luker, GD; Luker, KE; Moudgil, P; Nyati, S; Rehemtulla, A; Stacer, AC | 1 |
Borzym-Kluczyk, M; Cechowska-Pasko, M; Krętowski, R | 1 |
Anderson, KC; Hide, M; Hideshima, H; Hideshima, T; Ikeda, H; Iwasaki, A; Yoshida, Y | 1 |
Chen, JH; Guo, XL; Liu, XY; Wang, HY; Zhang, P; Zheng, BB | 1 |
Chen, J; Guo, X; Liu, X; Wang, H; Wang, W | 1 |
Bielawska, A; Bielawski, K; Czarnomysy, R; Gornowicz, A; Kałuża, Z; Lepiarczyk, M | 1 |
Acılan, C; Baykal, AT; Boyacı, I; Okur, E; Ulukaya, E; Yerlikaya, A | 1 |
Amin, HM; Angelo, LS; Falchook, GS; Hess, K; Hong, D; Howard, AN; Huang, M; Jackson, EF; Janku, F; Kurzrock, R; Lawhorn, KN; Naing, A; Ng, CS; Parkhurst, KL; Tannir, NM; Vishwamitra, D; Wheler, JJ | 1 |
Chang, HY; Chen, NN; Huang, HC; Huang, TC; Juan, HF | 1 |
Ahmed, M; Goldberg, SN; Kumar, G; Levchenko, T; Moussa, M; Sawant, RR; Torchilin, V | 1 |
Bouwman, P; Greco, D; Gu, Y; Jonkers, J; Kuznetsov, SG; Saarela, J; Yadav, B | 1 |
Hengstler, JG; Schad, A; Schmidt, M; Sleeman, JP; Thaler, S; Thiede, G | 1 |
Chirgwin, JM; Suvannasankha, A | 1 |
Beissbarth, T; Cormet-Boyaka, E; Dobbelstein, M; Edmunds, S; Gaedcke, J; Ghadimi, M; Krüger, E; Levine, AJ; Markert, E; Moll, UM; Schulz, R; Zhang, X | 1 |
Abdel-Fatah, TM; Aleskandarany, MA; Alsubhi, N; Arora, A; Chan, SY; Curtin, NJ; Doherty, R; Ellis, IO; Green, AR; Madhusudan, S; Martin, SG; Middleton, F; Moseley, PM; Rakha, EA; Stephens, P | 1 |
Ahmed, Y; Chen, H; Hu, L; Li, D; Li, Z; Negi, H; Wu, Z; Zheng, Y; Zhu, Q | 1 |
Chan, JY; Cui, G; Di, L; Lee, SM; Li, C; Shan, L; Wang, L; Wang, Y; Xu, C; Zhang, Q; Zhang, X | 1 |
Deng, O; Du, Z; Gao, J; Gorityala, S; Lai, J; Ma, Z; Susana, G; Xiong, X; Xu, Y; Yan, C; Yang, S; Zhang, J; Zhang, Y | 1 |
Fogarty, FM; Kennedy, RD; Lyons, A; McCabe, N; O'Connor, R; O'Flanagan, CH; O'Shea, S | 1 |
Cho, BR; Choi, JW; Han, MS; Hong, ST; Kang, DE; Lim, CS; Paik, KC | 1 |
Argyros, O; Christoforidis, S; Kouvari, E; Lougiakis, N; Marakos, P; Papafotika, A; Pouli, N; Psycharis, V; Raptopoulou, CP; Tamvakopoulos, C | 1 |
Bertoni, F; Capri, G; Catapano, CV; Cresta, S; Gallerani, E; Gianni, L; Maccioni, E; Maur, M; Passalacqua, D; Rinaldi, A; Sessa, C; Tosi, D; Viganò, L | 1 |
Erin, N; Yerlikaya, A | 1 |
Conti, AA; Dilaghi, B; Modesti, PA; Nozzoli, C | 1 |
Ames, E; Hallett, WH; Murphy, WJ | 1 |
Cao, X; Garofalo, A; Grande, F; Louie, S; Neamati, N; Oshima, T; Yamada, R | 1 |
Bottini, A; Generali, D; Harris, AL; Mellor, HR; Milani, M; Pike, L; Rzymski, T | 1 |
Gupta, M; Luker, G; Luker, K | 1 |
Agyin, JK; Nair, HB; Roy, SS; Santhamma, B; Tekmal, RR | 1 |
Anderson, KC; Buon, L; Charalambous, E; Chauhan, D; Clynes, M; Daskalaki, E; Hayden, PJ; Hideshima, T; Kotoula, V; McMillin, DW; Mitsiades, CS; Mitsiades, N; Munshi, NC; O'Gorman, P; Ooi, MG; Raje, NS; Richardson, PG | 1 |
Alarid, ET; Casa, AJ; Ellison-Zelski, SJ; Lee, AV; Powers, GL | 1 |
Dou, QP; Lonardo, F; Pass, HI; Puliyappadamba, VT; Rishi, AK; Ruckdeschel, JC; Sharma, S; Tarca, A; Wali, A; Wang, Y; Yang, H | 1 |
Barrett, JR; Bhalla, KN; Erickson, B; Ganapathy, V; Gopal, E; Hill, WD; Jackson, WH; Periyasamy-Thandavan, S; Raney, L; Samaddar, JS; Schoenlein, PV | 1 |
Chow, W; Cristea, M; Doroshow, JH; Frankel, P; Gaur, S; Koczywas, M; Lim, D; Luu, T; Margolin, K; Morgan, RJ; Somlo, G; Yen, Y | 1 |
Benz, CC; Gibson, BW; Held, JM; Marx, C | 1 |
Luo, J; Ma, C; Niu, X; Shao, Z; Shen, K | 1 |
Ayers, DC; Barthel, TK; Bouxsein, ML; Cheng, D; Hussain, S; Jones, MD; Lian, JB; Liu, JC; Lovria, E; Mukherjee, S; Mulay, S; Schoonmaker, JA; Stein, GS | 1 |
Bernard, PS; Carey, LA; Chiu, WK; Collichio, FA; Dees, EC; Irvin, WJ; Ivanova, A; Orlowski, RZ; Perou, C; Stijleman, IJ | 1 |
Aguirre-Ghiso, J; Bahadur, U; Germain, D; Ishii, Y; Papa, L; Shioda, T; Waxman, S; Yue, Z | 1 |
Amm, HM; Buchsbaum, DJ; Kuo, H; Li, Y; Steg, AD; Zhou, T | 1 |
Liu, X; Liu, Y; Zhang, JH; Zhang, Y; Zuo, T | 1 |
Oh, A; Yee, D; Zeng, X; Zhang, H; Zhang, Y | 1 |
Arshad Siddiqui, M; Belanger, DB; Bracken, JB; Curran, PJ; Malkowski, M; Miao, H; Shipps, GW; Wang, Y; Zeng, H | 1 |
Begus-Nahrmann, Y; Beissbarth, T; Eick, D; Gorsler, T; Hennion, M; Hintermair, C; Hsu, C; Johnsen, SA; Kramer, F; Kremmer, E; Prenzel, T; Simons, M | 1 |
Arteaga, CL; Balko, JM; Buck, E; Fox, EM; González-Angulo, AM; Kuba, MG; Liu, S; Manning, HC; Miller, TW; Mills, GB; Sánchez, V; Shyr, Y; Smith, RA; Ye, F | 1 |
Brnjic, S; D'Arcy, P; De Cesare, M; Fryknäs, M; Hassan, M; Larsson, R; Linder, S; Lindsten, K; Olofsson, MH; Perego, P; Sadeghi, B | 1 |
Hou, K; Liu, J; Liu, Y; Qu, J; Qu, X; Teng, Y; Xu, L; Zhang, L; Zhang, Y | 1 |
Brundage, RC; Hull, JM; Khatri, A; Kirstein, MN; Williams, BW; Yee, D | 1 |
De Mesmaeker, P; Deleu, I; Dirix, LY; Prové, A; Rasschaert, M; Sas, L; Tjalma, WA; Trinh, XB; Van Dam, PA; Van de Velde, H; Van Laere, SJ; Vermeulen, PB; Vinken, P; Wojtasik, A | 1 |
Masmiquel Comas, L; Nicolau Ramis, J | 1 |
Inazu, M; Itoh, M; Kohno, N; Komatsu, S; Miyazawa, K; Moriya, S; Naito, M; Takase, A; Tomoda, A | 1 |
Gartel, AL; Wang, M | 1 |
Okur, E; Ulukaya, E; Yerlikaya, A | 1 |
Stockler, MR; Wilcken, NR | 1 |
Amerik, AY; Issaenko, OA | 1 |
Chang, KC; Chen, KF; Chu, PY; Liu, CY; Shiau, CW; Tseng, LM | 1 |
Bracke, M; De Wever, O; Emami, S; Gespach, C; Hendrix, A; Hung, MC; Lambein, K; Land, D; Larsen, AK; Ouelaa-Benslama, R; Prévost, G; Sabbah, M | 1 |
Choi, KS; Kim, EH; Kwon, TK; Park, SA; Yoon, MJ | 1 |
Yerlikaya, A | 1 |
Gryczynski, Z; Ranjan, AP; Raut, SL; Thamake, SI; Vishwanatha, JK | 1 |
Cvek, B; Skrott, Z | 1 |
Basile, I; Cathiard, AM; Garcia, M; Gary-Bobo, M; Gleizes, M; Maynadier, M; Sheikh, MS; Shi, J; Vaillant, O; Wah, JL | 1 |
Brunton, VG; Idris, AI; Logan, JG; Marino, S; Muir, M; Sophocleous, A | 1 |
Aoyama, K; Hashimoto, K; Hibino, R; Inazuka, M; Ishikawa, T; Iwai, K; Kosugi, Y; Morimoto, M; Sumi, H; Tozawa, R; Yabuki, M; Yamamoto, S; Yamasaki, H; Yoshida, S; Yoshimatsu, M | 1 |
Bin Sun, H; Fei, X; Hutchins, GD; Lee Stone, K; Liu, X; Martinez, TD; Miller, KD; Mock, BH; Sledge, GW; Wang, JQ; Zheng, QH | 1 |
Dees, EC; Orlowski, RZ | 2 |
Cardoso, F; Durbecq, V; Picart, MJ; Ross, JS; Sotiriou, C | 1 |
Edmund, NA; Moore, DT; Orlowski, RZ; Shi, YY; Small, GW; Somasundaram, S | 1 |
Blasick, TM; Brown, RE; Lun, M; Siegelmann-Danieli, N; Zhang, PL | 2 |
Cooper, C; Liu, GY; Murphy, LC; Niu, YL; Santos, S; Watson, PH | 1 |
Bold, RJ; Fahy, BN; Mortenson, MM; Schlieman, MG; Virudachalam, S | 1 |
Bengston, AL; Denoyelle, C; Esteban, JA; Fernández, Y; Miller, TP; Soengas, MS; Tang, WH | 1 |
Booser, DJ; Broglio, KR; Cristofanilli, M; Esseltine, D; Gonzalez-Angulo, AM; Hortobagyi, GN; Islam, R; Krishnamurthy, S; Pusztai, L; Reuben, JM; Stec, J; Yang, CH | 1 |
Albanell, J; Bosch, M; Codony-Servat, J; Domingo-Domenech, J; Gascon, P; Mellado, B; Oliva, C; Rolfe, M; Ross, JS; Rovira, A; Tapia, MA | 1 |
Doihara, H; Fujita, T; Kawasaki, K; Ogasawara, Y; Shimizu, N; Takabatake, D; Takahashi, H; Tsukuda, K; Washio, K | 1 |
Orlowski, RZ; Shi, YY; Small, GW | 1 |
Alvarez, JV; Frank, DA; Germain, D; Ishii, Y; Keselman, I; Logothetis, D; Mandeli, J; O'Connell, MJ; Pirkmaier, A; Waxman, S | 1 |
Badran, B; Bex, F; Burny, A; Cardoso, F; Desmedt, C; Durbecq, V; Laes, JF; Lagneaux, L; Piccart, M; Ross, JS; Sotiriou, C; Willard-Gallo, K | 1 |
Banwait, S; Benz, CC; Hann, B; Marx, C; Park, JW; Scott, GK; Yau, C; Zhou, Y | 1 |
Jarois, T; Ju, D; Xie, Y; Xu, H | 1 |
Cheng, Y; Shen, P; Zhou, C | 1 |
Hatake, K | 1 |
Badve, S; Bergan, R; Brown, JA; Engel, RH; Gradishar, WJ; O'Regan, RM; Rademaker, A; Von Roenn, JH | 1 |
Nawasreh, M | 1 |
Adler, AS; Chang, HY; Lin, M; Nuyten, DS; Regev, A; Segal, E; van de Vijver, MJ; Wong, DJ | 1 |
Brossart, P; Freier, W; Greil, R; Kiewe, P; Kühnhardt, D; Kümmel, S; Lange, W; Lehenbauer-Dehm, S; Niederle, N; Possinger, K; Preiss, J; Regierer, A; Schippinger, W; Schmid, P; Van de Velde, H | 1 |
Albanell, J; Awada, A; Baselga, J; Canney, PA; Cardoso, F; Dirix, LY; Gascon, P; Gil, T; Piccart, MJ | 1 |
Adams, J; Ara, G; Herbst, R; Palombella, VJ; Teicher, BA | 1 |
Benson, AB; Dolan, ME; French, S; Mobarhan, S; Olopade, OI; Rademaker, A; Ratain, MJ; Stucky-Marshall, L | 1 |
Ali, IU; Herbert, BS; Kopelovich, L; Passons, CM; Shay, JW; Wright, AC; Wright, WE | 1 |
Freeman, JW; Gupta, RC; Smith, WA | 1 |
6 review(s) available for pyrazines and Breast Cancer
Article | Year |
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Combination treatment with CPX-351 and midostaurin in patients with secondary acute myeloid leukaemia that are FLT3 mutated: three cases and review of literature.
Topics: Aged; Allografts; Anemia, Refractory, with Excess of Blasts; Aniline Compounds; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Breast Neoplasms; Bridged Bicyclo Compounds, Heterocyclic; Clinical Trials, Phase III as Topic; Cytarabine; Daunorubicin; Fatal Outcome; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Liposomes; Male; Middle Aged; Myelodysplastic Syndromes; Neoplasm, Residual; Neoplasms, Radiation-Induced; Oncogene Proteins, Fusion; Peripheral Blood Stem Cell Transplantation; Point Mutation; Protein Kinase Inhibitors; Pyrazines; Remission Induction; Salvage Therapy; Staurosporine; Sulfonamides | 2020 |
Role of bone-anabolic agents in the treatment of breast cancer bone metastases.
Topics: Antineoplastic Agents; Bone Density Conservation Agents; Bone Neoplasms; Boronic Acids; Bortezomib; Breast Neoplasms; Everolimus; Female; Humans; Oligopeptides; Osteoblasts; Parathyroid Hormone; Proteasome Inhibitors; Pyrazines; Recombinant Fusion Proteins; Sirolimus; Thiophenes; Transforming Growth Factor beta | 2014 |
The role of the ubiquitination-proteasome pathway in breast cancer: applying drugs that affect the ubiquitin-proteasome pathway to the therapy of breast cancer.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Clinical Trials as Topic; Cysteine Endopeptidases; Female; Humans; Multienzyme Complexes; Proteasome Endopeptidase Complex; Pyrazines; Signal Transduction; Ubiquitins | 2003 |
Targeting the ubiquitin-proteasome pathway in breast cancer.
Topics: Animals; Boronic Acids; Bortezomib; Breast Neoplasms; Clinical Trials, Phase I as Topic; Clinical Trials, Phase II as Topic; Cysteine Endopeptidases; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Administration Schedule; Female; Humans; Mice; Molecular Biology; Multienzyme Complexes; Neoplasm Transplantation; NF-kappa B; Proteasome Endopeptidase Complex; Protein Transport; Pyrazines; Risk Factors; Sensitivity and Specificity; Survival Rate; Treatment Outcome; Ubiquitin | 2004 |
Targeting the ubiquitin-proteasome pathway in breast cancer therapy.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Drug Design; Female; Humans; Proteasome Endopeptidase Complex; Pyrazines; Signal Transduction; Ubiquitin | 2006 |
[Breast cancer and Her-2].
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Boronic Acids; Bortezomib; Brain Neoplasms; Breast Neoplasms; Clinical Trials as Topic; Drug Design; Drug Therapy, Combination; ErbB Receptors; Female; Gene Targeting; Humans; Lapatinib; Protease Inhibitors; Pyrazines; Quinazolines; Receptor, ErbB-2; Signal Transduction; Trastuzumab | 2007 |
10 trial(s) available for pyrazines and Breast Cancer
Article | Year |
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Targeting hypoxia-inducible factor-1α (HIF-1α) in combination with antiangiogenic therapy: a phase I trial of bortezomib plus bevacizumab.
Topics: Adult; Aged; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Protocols; Bevacizumab; Boronic Acids; Bortezomib; Breast Neoplasms; Carcinoma, Renal Cell; Fatigue; Female; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Kidney Neoplasms; Magnetic Resonance Imaging; Male; Middle Aged; Neoplasm Staging; Neovascularization, Pathologic; Proteasome Endopeptidase Complex; Pyrazines; Thrombocytopenia; Treatment Outcome; Vascular Endothelial Growth Factor A; Vascular Endothelial Growth Factor Receptor-2 | 2014 |
Phase I study of bortezomib with weekly paclitaxel in patients with advanced solid tumours.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Female; Humans; Infusions, Intravenous; Male; Maximum Tolerated Dose; Middle Aged; Ovarian Neoplasms; Paclitaxel; Prostatic Neoplasms; Pyrazines; Treatment Outcome | 2008 |
Phase I trial of fixed-dose rate gemcitabine in combination with bortezomib in advanced solid tumors.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Growth Processes; Cell Line, Tumor; Deoxycytidine; Dose-Response Relationship, Drug; Drug Administration Schedule; Drug Synergism; Gemcitabine; Humans; Middle Aged; Neoplasms; Pyrazines | 2010 |
Phase II study of bortezomib and pegylated liposomal doxorubicin in the treatment of metastatic breast cancer.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Dose-Response Relationship, Drug; Doxorubicin; Female; Follow-Up Studies; Humans; Middle Aged; Polyethylene Glycols; Pyrazines; Survival Analysis; Treatment Outcome | 2010 |
A phase II study of the combination of endocrine treatment and bortezomib in patients with endocrine-resistant metastatic breast cancer.
Topics: Aged; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Aromatase Inhibitors; Boronic Acids; Bortezomib; Breast Neoplasms; Cytokines; Drug Administration Schedule; Drug Resistance, Neoplasm; Female; Humans; Leukocytes, Mononuclear; Middle Aged; NF-kappa B; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Signal Transduction; Tamoxifen | 2012 |
Bortezomib (VELCADE) in metastatic breast cancer: pharmacodynamics, biological effects, and prediction of clinical benefits.
Topics: Adult; Aged; Bone Neoplasms; Boronic Acids; Bortezomib; Breast Neoplasms; Disease Progression; Disease-Free Survival; Female; Humans; Male; Maximum Tolerated Dose; Middle Aged; Pleural Neoplasms; Protease Inhibitors; Pyrazines; Receptors, Estrogen; Receptors, Progesterone; Soft Tissue Neoplasms; Survival Rate; Treatment Outcome | 2006 |
A phase II study of single agent bortezomib in patients with metastatic breast cancer: a single institution experience.
Topics: Adenocarcinoma; Adult; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Female; Humans; Middle Aged; Protease Inhibitors; Pyrazines; Treatment Outcome | 2007 |
A phase I/II study of bortezomib and capecitabine in patients with metastatic breast cancer previously treated with taxanes and/or anthracyclines.
Topics: Anthracyclines; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Capecitabine; Carcinoma; Deoxycytidine; Disease Progression; Drug Resistance, Neoplasm; Female; Fluorouracil; Hematologic Diseases; Humans; Maximum Tolerated Dose; Peripheral Nervous System Diseases; Pyrazines; Salvage Therapy; Survival Analysis; Taxoids; Treatment Outcome | 2008 |
Bortezomib/docetaxel combination therapy in patients with anthracycline-pretreated advanced/metastatic breast cancer: a phase I/II dose-escalation study.
Topics: Adult; Aged; Alopecia; Anthracyclines; Antibiotics, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Belgium; Boronic Acids; Bortezomib; Breast Neoplasms; Breast Neoplasms, Male; Diarrhea; Docetaxel; Drug Administration Schedule; Female; Humans; Male; Middle Aged; Nausea; Neutropenia; Prospective Studies; Pyrazines; Spain; Taxoids; Treatment Outcome; United Kingdom; Vomiting | 2008 |
Chronic daily low dose of 4-methyl-5-(2-pyrazinyl)-1,2-dithiole-3-thione (Oltipraz) in patients with previously resected colon polyps and first degree female relatives of breast cancer patients.
Topics: Anticarcinogenic Agents; Biopsy; Breast Neoplasms; Colonic Polyps; Dose-Response Relationship, Drug; Female; Glutathione; Glutathione Transferase; Hot Temperature; Humans; Lymphocytes; Male; Pyrazines; Rectum; Thiones; Thiophenes; Time Factors | 2000 |
98 other study(ies) available for pyrazines and Breast Cancer
Article | Year |
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Scaffold hopping of celastrol provides derivatives containing pepper ring, pyrazine and oxazole substructures as potent autophagy inducers against breast cancer cell line MCF-7.
Topics: Animals; Antineoplastic Agents; Apoptosis; Autophagy; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Female; Humans; MCF-7 Cells; Oxazoles; Pentacyclic Triterpenes; Pyrazines; Structure-Activity Relationship; Zebrafish | 2022 |
Design of Novel Imidazopyrazine Derivative against Breast Cancer
Topics: Antineoplastic Agents; Breast Neoplasms; Drug Design; Female; Humans; Imidazoles; Molecular Docking Simulation; Molecular Dynamics Simulation; Molecular Structure; Pyrazines; Receptors, Neuropeptide Y; Structure-Activity Relationship | 2023 |
WNT5B governs the phenotype of basal-like breast cancer by activating WNT signaling.
Topics: Antineoplastic Agents; Breast Neoplasms; Cell Line, Tumor; Female; Humans; Phenotype; Pyrazines; Pyridines; Wnt Proteins; Wnt Signaling Pathway | 2019 |
IGF-1R pathway activation as putative biomarker for linsitinib therapy to revert tamoxifen resistance in ER-positive breast cancer.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Biomarkers, Tumor; Breast Neoplasms; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Synergism; Female; Humans; Imidazoles; Immunohistochemistry; MAP Kinase Signaling System; MCF-7 Cells; Middle Aged; Neoplasm Staging; Phosphatidylinositol 3-Kinases; Phosphorylation; Pyrazines; Receptor, IGF Type 1; Receptors, Estrogen; Tamoxifen | 2020 |
Replication and ribosomal stress induced by targeting pyrimidine synthesis and cellular checkpoints suppress p53-deficient tumors.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Breast Neoplasms; Cell Cycle Checkpoints; Cell Proliferation; Checkpoint Kinase 1; Dihydroorotate Dehydrogenase; Female; Gene Expression Regulation, Neoplastic; Genes, erbB-2; HCT116 Cells; Humans; Leflunomide; MCF-7 Cells; Mice, Inbred BALB C; Mice, Inbred NOD; Mice, SCID; Mice, Transgenic; Oxidoreductases Acting on CH-CH Group Donors; Phenylurea Compounds; Protein Kinase Inhibitors; Pyrazines; Pyrimidines; Ribosomes; Signal Transduction; Tumor Suppressor Protein p53 | 2020 |
[Reversal effect of peptide-modified chitosan tetramethylpyrazine nanoparticles on multidrug resistance in tumor cells].
Topics: Breast Neoplasms; Chitosan; Doxorubicin; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Humans; Nanoparticles; Peptides; Pyrazines | 2020 |
Highly Bright NIR-BRET System for Imaging Molecular Events in Live Cells.
Topics: Animals; Apoptosis; Breast Neoplasms; Cell Proliferation; Female; Fluorescence Resonance Energy Transfer; Humans; Imidazoles; Luciferases; Luminescent Agents; Luminescent Measurements; Mice; Mice, Inbred NOD; Mice, SCID; Optical Imaging; Pyrazines; Spectroscopy, Near-Infrared; Tumor Cells, Cultured; Xenograft Model Antitumor Assays | 2021 |
Insulin-like growth factor-1 signaling is responsible for cathepsin G-induced aggregation of breast cancer MCF-7 cells.
Topics: Autocrine Communication; Axitinib; Breast Neoplasms; Cathepsin G; Cell Aggregation; Female; Humans; Imidazoles; Indazoles; Indoles; Insulin-Like Growth Factor I; MCF-7 Cells; Phosphorylation; Pyrazines; Pyrroles; Receptor, IGF Type 1; Receptors, Somatomedin; Signal Transduction; Small Molecule Libraries; Sunitinib | 2017 |
A novel agent attenuates cardiotoxicity and improves antitumor activity of doxorubicin in breast cancer cells.
Topics: Animals; Antineoplastic Agents; Blotting, Western; Breast Neoplasms; Cell Line; Cell Line, Tumor; Cell Survival; Doxorubicin; Endoplasmic Reticulum Stress; Humans; Lactates; Oxidative Stress; Pyrazines; Rats; Signal Transduction; Zebrafish | 2019 |
Highly bright and stable NIR-BRET with blue-shifted coelenterazine derivatives for deep-tissue imaging of molecular events
Topics: Amino Acid Sequence; Animals; Binding Sites; Breast Neoplasms; Chlorocebus aethiops; COS Cells; Female; Fluorescence Resonance Energy Transfer; HeLa Cells; Heterografts; Humans; Imidazoles; Liver Neoplasms; Luciferases; Luminescent Agents; Luminescent Measurements; Luminescent Proteins; Lung Neoplasms; Mice; Models, Molecular; Molecular Imaging; Protein Binding; Protein Interaction Domains and Motifs; Protein Structure, Secondary; Pyrazines; Receptors, Estrogen; Recombinant Fusion Proteins; Red Fluorescent Protein; Single-Cell Analysis | 2019 |
ATR mediates cisplatin resistance in 3D-cultured breast cancer cells via translesion DNA synthesis modulation.
Topics: A549 Cells; Antineoplastic Agents; Ataxia Telangiectasia Mutated Proteins; Autophagy; Breast Neoplasms; Cell Culture Techniques; Cellular Microenvironment; Cellular Senescence; Checkpoint Kinase 1; Cisplatin; DNA Damage; DNA Replication; DNA-Binding Proteins; DNA-Directed DNA Polymerase; Drug Resistance, Neoplasm; Female; Histones; Humans; MCF-7 Cells; Pyrazines; S Phase Cell Cycle Checkpoints; Sulfones; Tumor Cells, Cultured; Tumor Suppressor Protein p53 | 2019 |
Development of a quantitative method to measure EV uptake.
Topics: Biological Transport; Breast Neoplasms; Cell Line, Tumor; Extracellular Vesicles; Female; Genes, Reporter; Green Fluorescent Proteins; High-Throughput Screening Assays; Humans; Imidazoles; Luciferases, Renilla; Luminescent Measurements; Nanoparticles; Pyrazines; Recombinant Fusion Proteins; Sensitivity and Specificity; Subcellular Fractions; Tetraspanin 29; Tetraspanin 30 | 2019 |
Tandem multicomponent reactions toward the design and synthesis of novel antibacterial and cytotoxic motifs.
Topics: Anti-Bacterial Agents; Antineoplastic Agents; Bacteria; Bacterial Infections; Breast Neoplasms; Cell Line, Tumor; Female; Humans; Imidazoles; Melanoma; Pyrazines; Pyridines | 2013 |
Effect of bortezomib in combination with cisplatin and 5‑fluorouracil on 4T1 breast cancer cells.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Cell Survival; Cisplatin; Drug Synergism; Female; Fluorouracil; Humans; Inhibitory Concentration 50; Pyrazines | 2013 |
Combined treatment with SAHA, bortezomib, and clarithromycin for concomitant targeting of aggresome formation and intracellular proteolytic pathways enhances ER stress-mediated cell death in breast cancer cells.
Topics: Anilides; Animals; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Death; Cell Line, Tumor; Cell Proliferation; Clarithromycin; Drug Screening Assays, Antitumor; Endoplasmic Reticulum Stress; Female; Gene Expression Regulation, Neoplastic; Humans; Hydroxamic Acids; Inclusion Bodies; Intracellular Space; Mice; Proteolysis; Pyrazines; Transcription Factor CHOP; Vorinostat | 2013 |
Anticancer agent ukrain and bortezomib combination is synergistic in 4T1 breast cancer cells.
Topics: Antineoplastic Agents; Apoptosis; Berberine Alkaloids; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Drug Synergism; Female; Humans; Melanoma, Experimental; Phenanthridines; Pyrazines | 2014 |
Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonists.
Topics: Animals; Benzopyrans; Binding Sites; Breast Neoplasms; Cell Line, Tumor; Crystallography, X-Ray; Drug Design; Female; Half-Life; Humans; Inhibitor of Apoptosis Proteins; Mice; Molecular Dynamics Simulation; Protein Structure, Tertiary; Pyrazines; Pyrroles; RNA, Messenger; Stereoisomerism; Transplantation, Heterologous; Tumor Necrosis Factor-alpha | 2013 |
PKC?-dependent activation of the ubiquitin proteasome system is responsible for high glucose-induced human breast cancer MCF-7 cell proliferation, migration and invasion.
Topics: Acetophenones; Apoptosis; Benzopyrans; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Movement; Cell Proliferation; Female; Glucose; Humans; MCF-7 Cells; Phosphorylation; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Protein Kinase C-delta; Pyrazines; Ubiquitin | 2013 |
TRAP1 role in endoplasmic reticulum stress protection favors resistance to anthracyclins in breast carcinoma cells.
Topics: Anthracyclines; Antineoplastic Agents; Apoptosis; ATPases Associated with Diverse Cellular Activities; Blotting, Western; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Proliferation; Drug Resistance, Neoplasm; eIF-2 Kinase; Endoplasmic Reticulum Chaperone BiP; Endoplasmic Reticulum Stress; Female; Heat-Shock Proteins; HSP90 Heat-Shock Proteins; Humans; Phosphorylation; Proteasome Endopeptidase Complex; Pyrazines; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tumor Cells, Cultured | 2014 |
Changes in proteasome chymotrypsin-like activity during the development of human mammary and thyroid carcinomas.
Topics: Boronic Acids; Bortezomib; Breast; Breast Neoplasms; Chymotrypsin; Drug Resistance, Neoplasm; Female; Humans; Neoplasm Metastasis; Neoplasm Staging; Proteasome Endopeptidase Complex; Pyrazines; Thyroid Gland; Thyroid Neoplasms | 2013 |
NanoLuc reporter for dual luciferase imaging in living animals.
Topics: Animals; Breast Neoplasms; Cell Line; Disease Progression; Female; Heterografts; Imidazoles; Luciferases; Luciferases, Firefly; Luminescent Measurements; Mice; Molecular Imaging; Neoplasm Transplantation; Pyrazines; Signal Transduction; Substrate Specificity; Transfection; Transforming Growth Factor beta | 2013 |
Efficient induction of apoptosis by proteasome inhibitor: bortezomib in the human breast cancer cell line MDA-MB-231.
Topics: Antineoplastic Agents; Apoptosis; beta-Galactosidase; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line; Cell Line, Tumor; Cell Survival; Female; Fibroblasts; HSP70 Heat-Shock Proteins; Humans; Hypoxia; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines | 2014 |
IKKβ inhibitor in combination with bortezomib induces cytotoxicity in breast cancer cells.
Topics: Active Transport, Cell Nucleus; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Female; Humans; I-kappa B Kinase; I-kappa B Proteins; Imidazoles; MCF-7 Cells; NF-KappaB Inhibitor alpha; Phosphorylation; Pyrazines; Quinoxalines; Transcription Factor RelA | 2014 |
DLJ14, a novel chemo-sensitization agent, enhances therapeutic effects of adriamycin against MCF-7/A cells both in vitro and in vivo.
Topics: Animals; Antibiotics, Antineoplastic; Antineoplastic Agents, Phytogenic; Breast Neoplasms; Doxorubicin; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Herb-Drug Interactions; Humans; Ligusticum; MCF-7 Cells; Mice; Mice, Inbred BALB C; Mice, Nude; Phytotherapy; Plant Extracts; Pyrazines | 2014 |
Combination treatment of ligustrazine piperazine derivate DLJ14 and adriamycin inhibits progression of resistant breast cancer through inhibition of the EGFR/PI3K/Akt survival pathway and induction of apoptosis.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Apoptosis Regulatory Proteins; Breast Neoplasms; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Down-Regulation; Doxorubicin; Drug Resistance, Neoplasm; ErbB Receptors; Female; G2 Phase Cell Cycle Checkpoints; Humans; MCF-7 Cells; Membrane Potential, Mitochondrial; Mitochondria; Phosphatidylinositol 3-Kinase; Proto-Oncogene Proteins c-akt; Pyrazines; Signal Transduction | 2014 |
Cytotoxic activity of octahydropyrazin[2,1-a:5,4-a']diisoquinoline derivatives in human breast cancer cells.
Topics: Antineoplastic Agents; Apoptosis; Breast Neoplasms; Cell Survival; Cytotoxins; Dose-Response Relationship, Drug; Female; Humans; Isoquinolines; MCF-7 Cells; Membrane Potential, Mitochondrial; Pyrazines | 2015 |
A proteomic analysis of p53-independent induction of apoptosis by bortezomib in 4T1 breast cancer cell line.
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; DNA Replication; DNA, Neoplasm; Endoplasmic Reticulum Chaperone BiP; Energy Metabolism; Female; Humans; Proteasome Endopeptidase Complex; Protein Folding; Protein Processing, Post-Translational; Proteome; Proteomics; Pyrazines; Tumor Suppressor Protein p53 | 2015 |
Combination therapy targeting ectopic ATP synthase and 26S proteasome induces ER stress in breast cancer cells.
Topics: Aurovertins; Autophagy; Boronic Acids; Bortezomib; Breast Neoplasms; Calcium; Caspases; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Membrane; Cell Proliferation; Cyclin D3; eIF-2 Kinase; Electron Transport; Endoplasmic Reticulum Stress; Eukaryotic Initiation Factor-2; Female; Humans; Mitochondrial Proton-Translocating ATPases; Molecular Targeted Therapy; Phosphorylation; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Receptors, Purinergic; Tumor Stem Cell Assay; Ubiquitin; Unfolded Protein Response; Vacuoles | 2014 |
Radiofrequency ablation-induced upregulation of hypoxia-inducible factor-1α can be suppressed with adjuvant bortezomib or liposomal chemotherapy.
Topics: Animals; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Catheter Ablation; Chemotherapy, Adjuvant; Disease Models, Animal; Female; Hypoxia-Inducible Factor 1, alpha Subunit; Liposomes; Liver; Pyrazines; Rats; Rats, Inbred F344; Up-Regulation | 2014 |
Suppression of BRCA1 sensitizes cells to proteasome inhibitors.
Topics: Animals; Boronic Acids; Bortezomib; BRCA1 Protein; Breast Neoplasms; Cell Cycle; Cell Line, Tumor; Down-Regulation; Female; Gene Silencing; Humans; Mice; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Retinoblastoma Protein; RNA, Small Interfering; Signal Transduction | 2014 |
The proteasome inhibitor Bortezomib (Velcade) as potential inhibitor of estrogen receptor-positive breast cancer.
Topics: Animals; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Death; Cell Line, Tumor; Disease Models, Animal; ErbB Receptors; Estrogen Receptor alpha; Female; Gene Expression Regulation, Neoplastic; Humans; Mitogen-Activated Protein Kinases; Neoplasm Metastasis; Phosphatidylinositol 3-Kinases; Prognosis; Proteasome Inhibitors; Proto-Oncogene Proteins c-akt; Pyrazines; Receptor, ErbB-2; Receptors, Estrogen; Signal Transduction; TOR Serine-Threonine Kinases; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2015 |
MicroRNA-101 Suppresses Tumor Cell Proliferation by Acting as an Endogenous Proteasome Inhibitor via Targeting the Proteasome Assembly Factor POMP.
Topics: 3' Untranslated Regions; Animals; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor Proteins; Drug Resistance, Neoplasm; Estrogen Receptor alpha; Female; Gene Knockdown Techniques; HCT116 Cells; Hep G2 Cells; Humans; MCF-7 Cells; Mice; MicroRNAs; Molecular Chaperones; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; RNA, Small Interfering; Tumor Suppressor Protein p53 | 2015 |
Chk1 phosphorylated at serine345 is a predictor of early local recurrence and radio-resistance in breast cancer.
Topics: Ataxia Telangiectasia Mutated Proteins; Breast Neoplasms; Checkpoint Kinase 1; Cohort Studies; DNA Repair; DNA-Binding Proteins; Female; Gene Knockdown Techniques; Humans; Indoles; MCF-7 Cells; Neoplasm Recurrence, Local; Neoplasm Staging; Phosphorylation; Protein Kinases; Pyrazines; Pyridones; Radiation Tolerance; RNA Interference; RNA, Small Interfering; Serine; Sulfones; Up-Regulation | 2016 |
Binding of anterior gradient 2 and estrogen receptor-α: Dual critical roles in enhancing fulvestrant resistance and IGF-1-induced tumorigenesis of breast cancer.
Topics: Antibodies, Monoclonal; Antineoplastic Agents, Hormonal; Breast Neoplasms; Cell Cycle Checkpoints; Cell Movement; Cell Proliferation; Cell Transformation, Neoplastic; Drug Resistance, Neoplasm; Epithelial-Mesenchymal Transition; Estradiol; Estrogen Receptor alpha; Estrogen Receptor Antagonists; Female; Fulvestrant; Humans; Imidazoles; Insulin-Like Growth Factor I; MCF-7 Cells; Mucoproteins; Oncogene Proteins; Protein Binding; Proteins; Proteolysis; Pyrazines; RNA Interference; Signal Transduction; Time Factors; Transfection | 2016 |
A novel agent exerts antitumor activity in breast cancer cells by targeting mitochondrial complex II.
Topics: Adenosine Triphosphate; Animals; Antineoplastic Agents; Breast Neoplasms; Cell Cycle Checkpoints; Cell Proliferation; Cell Respiration; Dose-Response Relationship, Drug; Electron Transport Complex II; Energy Metabolism; Enzyme Inhibitors; Female; Humans; Lactates; MCF-7 Cells; Membrane Potential, Mitochondrial; Mice, Inbred BALB C; Mitochondria; Pyrazines; Reactive Oxygen Species; Signal Transduction; Time Factors; Tumor Burden | 2016 |
Targeting radioresistant breast cancer cells by single agent CHK1 inhibitor via enhancing replication stress.
Topics: Antineoplastic Agents; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Checkpoint Kinase 1; DNA Repair; Homologous Recombination; Humans; MCF-7 Cells; Phenylurea Compounds; Protein Kinase Inhibitors; Pyrazines; Radiation Tolerance; Radiation-Sensitizing Agents; Thiophenes; Urea | 2016 |
IGF-1R inhibition sensitizes breast cancer cells to ATM-related kinase (ATR) inhibitor and cisplatin.
Topics: Ataxia Telangiectasia Mutated Proteins; Biomarkers, Tumor; Breast Neoplasms; Cell Survival; Cisplatin; DNA Damage; Histones; Humans; Imidazoles; Inhibitory Concentration 50; MCF-7 Cells; Oncogenes; Phosphorylation; Pyrazines; Pyrazoles; Receptor, IGF Type 1; Receptors, Somatomedin; Recombinant Proteins; RNA, Small Interfering; Triazines | 2016 |
Two-Photon Tracer for Human Epidermal Growth Factor Receptor-2: Detection of Breast Cancer in a Live Tissue.
Topics: Animals; Benzofurans; Breast Neoplasms; Cell Line, Tumor; Fluorescent Dyes; Humans; Light; Mice, Inbred BALB C; Pyrazines; Receptor, ErbB-2; Recombinant Fusion Proteins | 2016 |
Design and synthesis of novel 7-aminosubstituted pyrido[2,3-b]pyrazines exhibiting anti-breast cancer activity.
Topics: Animals; Antineoplastic Agents; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Chemistry Techniques, Synthetic; Drug Design; Female; Humans; Mice; Phosphoinositide-3 Kinase Inhibitors; Pyrazines; Structure-Activity Relationship; Xenograft Model Antitumor Assays | 2017 |
Differential sensitivity of breast cancer and melanoma cells to proteasome inhibitor Velcade.
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Caspase 3; Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinase Inhibitor p21; Humans; Inhibitory Concentration 50; Melanoma; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Tumor Suppressor Protein p53 | 2008 |
New evidence in oncologic and cardiocirculatory medicine.
Topics: Antineoplastic Agents; Antineoplastic Agents, Alkylating; Antineoplastic Agents, Hormonal; Boronic Acids; Bortezomib; Breast Neoplasms; Cardiology; Diagnosis, Computer-Assisted; Drug Therapy, Combination; Evidence-Based Medicine; Female; Humans; Mammography; Medical Oncology; Melphalan; Multiple Myeloma; Prednisone; Pyrazines | 2009 |
Sensitization of human breast cancer cells to natural killer cell-mediated cytotoxicity by proteasome inhibition.
Topics: Animals; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Carcinoma; Cell Line, Tumor; Cell Proliferation; Cells, Cultured; Combined Modality Therapy; Cytotoxicity, Immunologic; Female; Humans; Immunotherapy, Adoptive; Killer Cells, Natural; Mice; Mice, SCID; Protease Inhibitors; Pyrazines; Receptors, Death Domain; RNA, Messenger; Xenograft Model Antitumor Assays | 2009 |
Combination effects of SC144 and cytotoxic anticancer agents.
Topics: Adenocarcinoma; Administration, Oral; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Breast Neoplasms; Cell Line, Tumor; Cell Survival; Colorectal Neoplasms; Cytotoxins; Drug Screening Assays, Antitumor; Drug Synergism; Female; Humans; Inhibitory Concentration 50; Injections, Intraperitoneal; Mice; Mice, Nude; Organoplatinum Compounds; Paclitaxel; Pyrazines; Quinoxalines; Xenograft Model Antitumor Assays | 2009 |
The role of ATF4 stabilization and autophagy in resistance of breast cancer cells treated with Bortezomib.
Topics: Activating Transcription Factor 4; Antineoplastic Agents; Autophagy; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Division; Cell Line, Tumor; Female; Flow Cytometry; Humans; Immunohistochemistry; Neoplasm Proteins; Polymerase Chain Reaction; Pyrazines; RNA, Neoplasm; RNA, Small Interfering | 2009 |
Bioluminescent CXCL12 fusion protein for cellular studies of CXCR4 and CXCR7.
Topics: Animals; Biological Assay; Breast Neoplasms; Cell Line; Cell Line, Tumor; Chemokine CXCL12; Copepoda; Drug Discovery; Female; Genetic Vectors; Green Fluorescent Proteins; Humans; Imidazoles; Kidney; Lentivirus; Luciferases; Luminescent Measurements; Luminescent Proteins; Promoter Regions, Genetic; Protein Binding; Pyrazines; Receptors, CXCR; Receptors, CXCR4; Recombinant Fusion Proteins; Signal Transduction; Substrate Specificity; Transduction, Genetic | 2009 |
BU-32: a novel proteasome inhibitor for breast cancer.
Topics: Animals; Apoptosis; Bone Neoplasms; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Growth Processes; Cell Line, Tumor; Chymotrypsin; Female; Gene Expression Regulation, Neoplastic; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; NF-kappa B; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Pyrazoles; Xenograft Model Antitumor Assays | 2009 |
Interactions of the Hdm2/p53 and proteasome pathways may enhance the antitumor activity of bortezomib.
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Carcinoma; Cell Line, Tumor; Cell Survival; Humans; Imidazoles; Multiple Myeloma; Mutation, Missense; Neoplasms, Glandular and Epithelial; Piperazines; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Proto-Oncogene Proteins c-mdm2; Pyrazines; Tumor Suppressor Protein p53 | 2009 |
Proteasome inhibition represses ERalpha gene expression in ER+ cells: a new link between proteasome activity and estrogen signaling in breast cancer.
Topics: Blotting, Western; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Chymotrypsin; Dose-Response Relationship, Drug; Estrogen Receptor alpha; Estrogens; Female; Gene Expression Regulation, Neoplastic; Humans; Kinetics; Promoter Regions, Genetic; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Reverse Transcriptase Polymerase Chain Reaction; RNA Polymerase II; Signal Transduction | 2010 |
Targeted proteasome inhibition by Velcade induces apoptosis in human mesothelioma and breast cancer cell lines.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Blotting, Western; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Cycle; Cell Line, Tumor; Cisplatin; Dose-Response Relationship, Drug; Drug Delivery Systems; Drug Synergism; Female; Flow Cytometry; Humans; Mesothelioma; Pilot Projects; Protease Inhibitors; Proteasome Inhibitors; Pyrazines; Signal Transduction; Time Factors | 2010 |
Bortezomib blocks the catabolic process of autophagy via a cathepsin-dependent mechanism, affects endoplasmic reticulum stress and induces caspase-dependent cell death in antiestrogen-sensitive and resistant ER+ breast cancer cells.
Topics: Antineoplastic Agents; Autophagy; Boronic Acids; Bortezomib; Breast Neoplasms; Caspases; Cathepsins; Cell Death; Down-Regulation; Drug Evaluation, Preclinical; Drug Resistance, Neoplasm; Endoplasmic Reticulum; Endoplasmic Reticulum Chaperone BiP; Estrogen Receptor Modulators; Female; Humans; Metabolism; Pyrazines; Receptors, Estrogen; Signal Transduction; Stress, Physiological; Tumor Cells, Cultured | 2010 |
ErbB2 trafficking and degradation associated with K48 and K63 polyubiquitination.
Topics: Benzoquinones; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Clathrin; Down-Regulation; HSP90 Heat-Shock Proteins; Humans; Lactams, Macrocyclic; Lysosomes; Mass Spectrometry; Microscopy, Fluorescence; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Receptor, ErbB-2; Ubiquitination | 2010 |
Combined effects of lapatinib and bortezomib in human epidermal receptor 2 (HER2)-overexpressing breast cancer cells and activity of bortezomib against lapatinib-resistant breast cancer cells.
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cyclin-Dependent Kinase Inhibitor p27; Drug Resistance, Neoplasm; Extracellular Signal-Regulated MAP Kinases; Female; Humans; Intracellular Signaling Peptides and Proteins; Lapatinib; Phosphorylation; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-akt; Pyrazines; Quinazolines; Receptor, ErbB-2 | 2010 |
A proteasome inhibitor, bortezomib, inhibits breast cancer growth and reduces osteolysis by downregulating metastatic genes.
Topics: Animals; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Growth Processes; Cell Line, Tumor; Down-Regulation; Female; Fluorodeoxyglucose F18; Gene Expression Regulation, Neoplastic; Humans; Mice; Mice, SCID; Neoplasm Metastasis; Osteolysis; Positron-Emission Tomography; Protease Inhibitors; Pyrazines; Radiopharmaceuticals; Xenograft Model Antitumor Assays | 2010 |
Bortezomib enhances the efficacy of fulvestrant by amplifying the aggregation of the estrogen receptor, which leads to a proapoptotic unfolded protein response.
Topics: Animals; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Blotting, Western; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Nucleus; Cytoplasm; Drug Resistance, Neoplasm; Drug Synergism; Estradiol; Female; Fluorescent Antibody Technique; Fulvestrant; Green Fluorescent Proteins; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Pyrazines; Receptors, Estrogen; Tamoxifen; Tumor Burden; Unfolded Protein Response; Xenograft Model Antitumor Assays | 2011 |
Mechanisms of drug sensitization to TRA-8, an agonistic death receptor 5 antibody, involve modulation of the intrinsic apoptotic pathway in human breast cancer cells.
Topics: Animals; Antibodies, Monoclonal; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Azocines; Benzhydryl Compounds; Boronic Acids; Bortezomib; Breast Neoplasms; Caspases; Cell Line, Tumor; Doxorubicin; Drug Resistance, Neoplasm; Female; Genes, bcl-2; Gossypol; Humans; Mice; Pyrazines; Receptors, TNF-Related Apoptosis-Inducing Ligand; Tumor Cells, Cultured | 2011 |
Tetramethylpyrazine reverses multidrug resistance in breast cancer cells through regulating the expression and function of P-glycoprotein.
Topics: Adenosine Triphosphatases; Antibiotics, Antineoplastic; ATP Binding Cassette Transporter, Subfamily B; Blotting, Western; Breast Neoplasms; Cell Proliferation; Doxorubicin; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Flow Cytometry; Gene Expression Regulation, Neoplastic; Humans; Pyrazines; Real-Time Polymerase Chain Reaction; RNA, Messenger; Tumor Cells, Cultured; Vasodilator Agents | 2012 |
Enhancement of doxorubicin cytotoxicity of human cancer cells by tyrosine kinase inhibition of insulin receptor and type I IGF receptor.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Autophagy; Breast Neoplasms; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Doxorubicin; Drug Synergism; Female; Humans; Imidazoles; Inhibitory Concentration 50; Mice; Mice, Nude; Pyrazines; Receptor, IGF Type 1; Receptor, Insulin; Signal Transduction; Tumor Burden; Xenograft Model Antitumor Assays | 2012 |
Discovery of novel imidazo[1,2-a]pyrazin-8-amines as Brk/PTK6 inhibitors.
Topics: Adaptor Proteins, Signal Transducing; Animals; Aurora Kinases; Breast Neoplasms; Computer Simulation; Dasatinib; DNA-Binding Proteins; Dose-Response Relationship, Drug; Drug Design; Drug Discovery; Drug Screening Assays, Antitumor; Female; Humans; Imidazoles; Inhibitory Concentration 50; Melanocytes; Mice; Molecular Targeted Therapy; Neoplasm Proteins; Oncogenes; Phenotype; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Protein-Tyrosine Kinases; Proto-Oncogenes; Pyrazines; Pyrimidines; RNA-Binding Proteins; Structure-Activity Relationship; Thiazoles | 2011 |
Estrogen-dependent gene transcription in human breast cancer cells relies upon proteasome-dependent monoubiquitination of histone H2B.
Topics: Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Estrogens; Female; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Histones; Humans; Neoplasms, Hormone-Dependent; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Transcription, Genetic; Ubiquitination | 2011 |
A kinome-wide screen identifies the insulin/IGF-I receptor pathway as a mechanism of escape from hormone dependence in breast cancer.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents, Hormonal; Breast Neoplasms; Cell Line, Tumor; Disease-Free Survival; Estradiol; Estrogen Receptor Modulators; Estrogens; Female; Fulvestrant; Gene Expression Regulation, Neoplastic; Humans; Imidazoles; Insulin; Insulin-Like Growth Factor I; Mice; Mice, Nude; Neoplasm Proteins; Neoplasms, Hormone-Dependent; Protein-Tyrosine Kinases; Pyrazines; Random Allocation; Receptor, IGF Type 1; Receptor, Insulin; Receptors, Estrogen; RNA Interference; Signal Transduction; Tamoxifen; Xenograft Model Antitumor Assays | 2011 |
Inhibition of proteasome deubiquitinating activity as a new cancer therapy.
Topics: Animals; Antineoplastic Agents; Apoptosis; bcl-2-Associated X Protein; Boronic Acids; Bortezomib; Breast Neoplasms; Carboxypeptidases; Cell Line, Tumor; Disease Models, Animal; Female; Gene Expression Regulation, Enzymologic; Humans; Mice; Mice, Inbred BALB C; Mice, SCID; Microarray Analysis; Multiple Myeloma; Piperidones; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Tumor Suppressor Protein p53; Ubiquitin; Ubiquitin Thiolesterase; Ubiquitination | 2011 |
Proteasome inhibitor bortezomib (PS-341) enhances RANKL-induced MDA-MB-231 breast cancer cell migration.
Topics: Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Movement; Female; Humans; Protease Inhibitors; Proto-Oncogene Proteins c-akt; Pyrazines; RANK Ligand; Receptor Activator of Nuclear Factor-kappa B; Up-Regulation | 2012 |
Pharmacodynamic modeling of sequence-dependent antitumor activity of insulin-like growth factor blockade and gemcitabine.
Topics: Antineoplastic Combined Chemotherapy Protocols; Bayes Theorem; Breast Neoplasms; Cell Line, Tumor; Deoxycytidine; Drug Administration Schedule; Female; Gemcitabine; Humans; Imidazoles; Models, Biological; Pyrazines; Receptor, IGF Type 1; Signal Transduction; Somatomedins | 2012 |
[The new antidiabetic agents in the firing line.... safety reasons or witch hunt?].
Topics: Animals; Breast Neoplasms; Calcitonin; Carcinoma, Medullary; Clinical Trials as Topic; Comorbidity; Diabetes Mellitus, Type 2; Dipeptidyl Peptidase 4; Disease Susceptibility; Female; Glucagon-Like Peptide 1; Humans; Hypoglycemic Agents; Infections; Liraglutide; Pancreatitis; Pharmacovigilance; Pioglitazone; Pyrazines; Risk Assessment; Safety-Based Drug Withdrawals; Sitagliptin Phosphate; Species Specificity; Thiazolidinediones; Thyroid Neoplasms; Triazoles; Urinary Bladder Neoplasms | 2012 |
Clarithromycin enhances bortezomib-induced cytotoxicity via endoplasmic reticulum stress-mediated CHOP (GADD153) induction and autophagy in breast cancer cells.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Autophagy; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Clarithromycin; Cytotoxicity, Immunologic; Drug Synergism; Endoplasmic Reticulum; Endoplasmic Reticulum Chaperone BiP; Female; Gene Expression; Humans; Pyrazines; Transcription Factor CHOP | 2012 |
Combination with bortezomib enhances the antitumor effects of nanoparticle-encapsulated thiostrepton.
Topics: Adenocarcinoma; Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Drug Synergism; Female; Humans; Male; Mice; Mice, Nude; Nanocapsules; Proteasome Endopeptidase Complex; Pyrazines; Random Allocation; Thiostrepton; Tissue Distribution; Tumor Burden; Xenograft Model Antitumor Assays | 2012 |
The p53-independent induction of apoptosis in breast cancer cells in response to proteasome inhibitor bortezomib.
Topics: Antineoplastic Agents; Apoptosis; Apoptosis Regulatory Proteins; Boronic Acids; Bortezomib; Breast Neoplasms; Caspase 3; Cell Line, Tumor; Enzyme Activation; Female; Gene Expression Regulation, Neoplastic; Humans; Pyrazines; Tumor Suppressor Protein p53 | 2012 |
Why is management of cancer pain still a problem?
Topics: Analgesics; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Colorectal Neoplasms; Female; Healthcare Disparities; Humans; Lung Neoplasms; Male; Multiple Myeloma; Pain Management; Practice Patterns, Physicians'; Prostatic Neoplasms; Pyrazines | 2012 |
Chalcone-based small-molecule inhibitors attenuate malignant phenotype via targeting deubiquitinating enzymes.
Topics: Antineoplastic Agents; Apoptosis; Benzylidene Compounds; Boronic Acids; Bortezomib; Breast Neoplasms; Catalytic Domain; Cell Cycle Checkpoints; Cell Proliferation; Cell Survival; Chalcone; Cyclin D1; Cysteine; Dose-Response Relationship, Drug; Endopeptidases; Female; HeLa Cells; Humans; Ovarian Neoplasms; Phenotype; Piperidones; Protease Inhibitors; Proteasome Endopeptidase Complex; Pyrazines; Tumor Suppressor Protein p53; Ubiquitin Thiolesterase; Ubiquitins | 2012 |
CIP2A is a target of bortezomib in human triple negative breast cancer cells.
Topics: Animals; Antineoplastic Agents; Apoptosis; Autoantigens; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Dose-Response Relationship, Drug; Drug Resistance, Neoplasm; Female; Humans; Intracellular Signaling Peptides and Proteins; MCF-7 Cells; Membrane Proteins; Mice; Mice, Nude; Proteasome Inhibitors; Proto-Oncogene Proteins c-akt; Pyrazines; Receptors, Estrogen; Xenograft Model Antitumor Assays | 2012 |
Identification of a GαGβγ, AKT and PKCα signalome associated with invasive growth in two genetic models of human breast cancer cell epithelial-to-mesenchymal transition.
Topics: Biomarkers, Tumor; Breast Neoplasms; CCN Intercellular Signaling Proteins; Cell Line, Tumor; Cell Movement; Cell Proliferation; Cyclohexanes; Epithelial-Mesenchymal Transition; Female; Gene Expression Profiling; Gene Knockdown Techniques; Heterotrimeric GTP-Binding Proteins; Humans; Mitogen-Activated Protein Kinases; Pertussis Toxin; Phenotype; Prognosis; Protein Kinase C-alpha; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-akt; Pyrazines; Repressor Proteins; RNA Interference; Signal Transduction; Snail Family Transcription Factors; Transcription Factors; Xanthenes | 2012 |
Simultaneous mitochondrial Ca(2+) overload and proteasomal inhibition are responsible for the induction of paraptosis in malignant breast cancer cells.
Topics: Antineoplastic Agents, Phytogenic; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Calcium; Cell Death; Cell Line, Tumor; Clonazepam; Curcumin; Dose-Response Relationship, Drug; Endoplasmic Reticulum; Female; Humans; Mitochondria; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Sodium-Calcium Exchanger; Thiazepines; Time Factors | 2012 |
Expression of heme oxygenase-1 in response to proteasomal inhibition.
Topics: Animals; Base Sequence; Blotting, Western; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Dose-Response Relationship, Drug; Enzyme Induction; Female; Genes, p53; Heme Oxygenase-1; Humans; Leupeptins; Melanoma, Experimental; Mice; Molecular Sequence Data; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Regulatory Sequences, Nucleic Acid | 2012 |
Alendronate coated poly-lactic-co-glycolic acid (PLGA) nanoparticles for active targeting of metastatic breast cancer.
Topics: Alendronate; Animals; Antineoplastic Agents; Bone and Bones; Bone Neoplasms; Boronic Acids; Bortezomib; Breast Neoplasms; Curcumin; Drug Carriers; Female; Humans; Lactic Acid; Mice; Mice, Nude; Nanoparticles; Neoplasm Metastasis; Osteoporosis; Polyglycolic Acid; Polylactic Acid-Polyglycolic Acid Copolymer; Pyrazines | 2012 |
Diethyldithiocarbamate complex with copper: the mechanism of action in cancer cells.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Coordination Complexes; Copper; Ditiocarb; Humans; Oxidative Stress; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines | 2012 |
Roles of estrogen receptor and p21(Waf1) in bortezomib-induced growth inhibition in human breast cancer cells.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Growth Processes; Cell Line, Tumor; Cyclin-Dependent Kinase Inhibitor p21; Estrogen Receptor alpha; Female; HCT116 Cells; Humans; MCF-7 Cells; Pyrazines; Tumor Cells, Cultured; Tumor Suppressor Protein p53 | 2012 |
Selective tyrosine kinase inhibition of insulin-like growth factor-1 receptor inhibits human and mouse breast cancer-induced bone cell activity, bone remodeling, and osteolysis.
Topics: Animals; Bone Remodeling; Breast Neoplasms; Cell Line, Tumor; Female; Humans; Imidazoles; Mice; Osteoclasts; Osteolysis; Protein-Tyrosine Kinases; Pyrazines; Receptor, IGF Type 1 | 2013 |
Antitumor activity and pharmacodynamic biomarkers of a novel and orally available small-molecule antagonist of inhibitor of apoptosis proteins.
Topics: Animals; Apoptosis; Biomarkers, Tumor; Breast Neoplasms; Caspases; Cell Line; Cell Survival; Humans; Inhibitor of Apoptosis Proteins; Mice; Mice, Inbred BALB C; Mice, Nude; Oligopeptides; Pyrazines; Signal Transduction; Tumor Cells, Cultured; Tumor Necrosis Factor-alpha; Tumor Necrosis Factors | 2013 |
Synthesis and preliminary biological evaluation of MMP inhibitor radiotracers [11C]methyl-halo-CGS 27023A analogs, new potential PET breast cancer imaging agents.
Topics: Animals; Biomarkers, Tumor; Breast Neoplasms; Carbon Radioisotopes; Humans; Hydroxamic Acids; Metalloendopeptidases; Protease Inhibitors; Pyrazines; Radiopharmaceuticals; Sulfonamides; Tomography, Emission-Computed | 2002 |
Evidence that mitogen-activated protein kinase phosphatase-1 induction by proteasome inhibitors plays an antiapoptotic role.
Topics: Animals; Apoptosis; Boronic Acids; Bortezomib; Breast; Breast Neoplasms; Cell Cycle Proteins; Cell Line; Cell Line, Transformed; Cell Line, Tumor; Dual Specificity Phosphatase 1; Fibroblasts; Genes, myc; Humans; Immediate-Early Proteins; Mice; Mice, Knockout; Mice, Nude; Phosphoprotein Phosphatases; Protease Inhibitors; Proteasome Endopeptidase Complex; Protein Phosphatase 1; Protein Tyrosine Phosphatases; Pyrazines; Recombinant Proteins; Transplantation, Heterologous | 2004 |
Pamidronate resistance and associated low ras levels in breast cancer cells: a role for combinatorial therapy.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Benzamides; Boronic Acids; Bortezomib; Breast Neoplasms; Carcinoma; Cell Line, Tumor; Cell Proliferation; Diphosphonates; Drug Combinations; Drug Resistance, Neoplasm; Female; Humans; Imatinib Mesylate; Pamidronate; Piperazines; Pyrazines; Pyrimidines; ras Proteins; Sirolimus | 2004 |
Intermittent hypoxia induces proteasome-dependent down-regulation of estrogen receptor alpha in human breast carcinoma.
Topics: Antigens, Neoplasm; Blotting, Western; Boronic Acids; Bortezomib; Breast Neoplasms; Carbonic Anhydrase IX; Carbonic Anhydrases; Carcinoma, Intraductal, Noninfiltrating; Cell Hypoxia; Cell Survival; Down-Regulation; Estrogen Receptor alpha; Female; Glucose Transporter Type 1; Humans; Immunoenzyme Techniques; Monosaccharide Transport Proteins; Neoplasm Invasiveness; Oxygen; Protease Inhibitors; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Tumor Cells, Cultured | 2004 |
Targeting BCL-2 overexpression in various human malignancies through NF-kappaB inhibition by the proteasome inhibitor bortezomib.
Topics: Boronic Acids; Bortezomib; Breast Neoplasms; Cyclin D1; Female; Gene Expression Regulation, Neoplastic; Humans; Male; NF-kappa B; Pancreatic Neoplasms; Prostatic Neoplasms; Protease Inhibitors; Pyrazines; Signal Transduction; Transcription, Genetic; Tumor Cells, Cultured | 2005 |
Intracellular inhibitory effects of Velcade correlate with morphoproteomic expression of phosphorylated-nuclear factor-kappaB and p53 in breast cancer cell lines.
Topics: Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Division; Cell Line, Tumor; Female; Gene Expression Regulation, Neoplastic; Humans; NF-kappa B; Phosphorylation; Protease Inhibitors; Proteome; Pyrazines; Tumor Suppressor Protein p53 | 2005 |
Chemical blockage of the proteasome inhibitory function of bortezomib: impact on tumor cell death.
Topics: 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt; Antineoplastic Agents; Antioxidants; Binding, Competitive; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Death; Cell Line; Cell Line, Tumor; Cell Survival; Drug Antagonism; Fibroblasts; Free Radicals; Humans; Immunoblotting; Kinetics; Leupeptins; Melanocytes; Melanoma; Membrane Potentials; Models, Biological; Protease Inhibitors; Proteasome Inhibitors; Pyrazines; Reactive Oxygen Species; Skin; Time Factors | 2006 |
Differential cellular and molecular effects of bortezomib, a proteasome inhibitor, in human breast cancer cells.
Topics: Boronic Acids; Bortezomib; Breast Neoplasms; Cell Cycle Proteins; Cell Line, Tumor; Cell Survival; Cysteine Proteinase Inhibitors; Drug Resistance, Neoplasm; Dual Specificity Phosphatase 1; Enzyme Activation; ErbB Receptors; Female; Humans; Immediate-Early Proteins; MAP Kinase Kinase 4; MAP Kinase Kinase Kinases; Mitogen-Activated Protein Kinase 1; Phosphoprotein Phosphatases; Phosphorylation; Proteasome Inhibitors; Protein Phosphatase 1; Protein Serine-Threonine Kinases; Protein Tyrosine Phosphatases; Proto-Oncogene Proteins c-akt; Pyrazines; raf Kinases; Receptor Protein-Tyrosine Kinases; Receptor, ErbB-2 | 2006 |
Proteasome inhibitor bortezomib increases PTEN expression and enhances trastuzumab-induced growth inhibition in trastuzumab-resistant cells.
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Proliferation; Drug Interactions; Drug Resistance; Drug Resistance, Neoplasm; Female; Humans; Protease Inhibitors; Proteasome Inhibitors; PTEN Phosphohydrolase; Pyrazines; Trastuzumab | 2006 |
Proteasome inhibitors induce a p38 mitogen-activated protein kinase (MAPK)-dependent anti-apoptotic program involving MAPK phosphatase-1 and Akt in models of breast cancer.
Topics: Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Cycle Proteins; Cell Line, Transformed; Cell Line, Tumor; Dual Specificity Phosphatase 1; Female; Humans; Immediate-Early Proteins; p38 Mitogen-Activated Protein Kinases; Phosphoprotein Phosphatases; Protease Inhibitors; Protein Phosphatase 1; Protein Tyrosine Phosphatases; Proto-Oncogene Proteins c-akt; Pyrazines | 2006 |
Cyclin D1 overexpression and response to bortezomib treatment in a breast cancer model.
Topics: Animals; Antineoplastic Agents; Apoptosis; bcl-X Protein; Biomarkers, Tumor; Boronic Acids; Bortezomib; Breast Neoplasms; Calcium; Caspase 3; Caspases; Cell Line, Tumor; Cell Proliferation; Cyclin D1; Female; Fluorescent Antibody Technique; Gene Expression Regulation, Neoplastic; Humans; Immunoblotting; In Situ Nick-End Labeling; Mice; Mice, Inbred BALB C; Microarray Analysis; Protease Inhibitors; Proteasome Endopeptidase Complex; Pyrazines; STAT3 Transcription Factor; Transplantation, Heterologous; Up-Regulation | 2006 |
Bortezomib (PS-341, Velcade) increases the efficacy of trastuzumab (Herceptin) in HER-2-positive breast cancer cells in a synergistic manner.
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Nucleus; Cyclin-Dependent Kinase Inhibitor p27; Drug Resistance, Neoplasm; Drug Synergism; Humans; NF-kappa B; Pyrazines; Receptor, ErbB-2; Trastuzumab | 2006 |
Proteasome-regulated ERBB2 and estrogen receptor pathways in breast cancer.
Topics: Antineoplastic Agents; Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Drug Therapy, Combination; Humans; Oxidation-Reduction; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Pyrazines; Receptor, ErbB-2; Receptors, Estrogen; Transcription, Genetic | 2007 |
Diminished feedback regulation of proteasome expression and resistance to proteasome inhibitors in breast cancer cells.
Topics: Apoptosis; Boronic Acids; Bortezomib; Breast Neoplasms; Cell Line, Tumor; Cell Survival; Dose-Response Relationship, Drug; Drug Resistance, Neoplasm; Feedback, Physiological; Humans; Leupeptins; Protease Inhibitors; Proteasome Endopeptidase Complex; Pyrazines; Reverse Transcriptase Polymerase Chain Reaction; Temperature; Tetrazolium Salts; Thiazoles | 2008 |
Quantitative study of the drug efflux kinetics from sensitive and MDR human breast cancer cells.
Topics: Antibiotics, Antineoplastic; Biological Transport; Breast Neoplasms; Calcium Channel Blockers; Cell Line, Tumor; Diffusion; Doxorubicin; Drug Resistance, Multiple; Female; Humans; Kinetics; Microelectrodes; Models, Biological; Pyrazines; Verapamil | 2007 |
Chemo-, regio-, and stereoselectivity of F-ring opening reactions in the cephalostatin series.
Topics: Antineoplastic Agents; Boranes; Breast Neoplasms; Cell Line, Tumor; Drug Screening Assays, Antitumor; Humans; Liver Neoplasms; Phenazines; Pyrazines; Spiro Compounds; Steroids; Stomach Neoplasms; Structure-Activity Relationship | 2008 |
Revealing targeted therapy for human cancer by gene module maps.
Topics: Algorithms; Antineoplastic Agents; Boronic Acids; Bortezomib; Breast Neoplasms; Chromosome Mapping; Electronic Data Processing; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Gene Regulatory Networks; Gene Targeting; Genes, Mitochondrial; Genetic Therapy; Humans; Neoplasm Invasiveness; Neoplasms; Oligonucleotide Array Sequence Analysis; Prognosis; Proteasome Endopeptidase Complex; Pyrazines; Tumor Cells, Cultured; Wounds and Injuries | 2008 |
The proteasome inhibitor PS-341 in cancer therapy.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Bortezomib; Breast Neoplasms; Cisplatin; Cyclophosphamide; Dipeptides; Drug Synergism; Humans; Mammary Neoplasms, Experimental; Mice; Mice, Inbred BALB C; Protease Inhibitors; Pyrazines; Radiation-Sensitizing Agents; Tumor Cells, Cultured; Ubiquitins | 1999 |
Effects of chemopreventive and antitelomerase agents on the spontaneous immortalization of breast epithelial cells.
Topics: Antineoplastic Agents; Breast; Breast Neoplasms; Cell Division; Cell Transformation, Neoplastic; Cells, Cultured; Disease Progression; DNA, Complementary; Eflornithine; Enzyme Activation; Enzyme Inhibitors; Epithelial Cells; Female; Humans; Li-Fraumeni Syndrome; Oligodeoxyribonucleotides, Antisense; Point Mutation; Pyrazines; Reverse Transcriptase Inhibitors; Tamoxifen; Telomerase; Thiones; Thiophenes; Transformation, Genetic; Tretinoin | 2001 |
Effect of chemopreventive agents on DNA adduction induced by the potent mammary carcinogen dibenzo[a,l]pyrene in the human breast cells MCF-7.
Topics: Anticarcinogenic Agents; Antimutagenic Agents; Antineoplastic Agents; Benzopyrenes; Breast; Breast Neoplasms; Carcinogens; Cell Line; Chemoprevention; Chlorophyllides; DNA Adducts; Dose-Response Relationship, Drug; Female; Humans; Pyrazines; Thiones; Thiophenes | 2001 |