4-aminobenzoic acid has been researched along with rg7388 in 55 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 40 (72.73) | 24.3611 |
2020's | 15 (27.27) | 2.80 |
Authors | Studies |
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Bartkovitz, D; Chu, XJ; Ding, Q; Filipovic, ZM; Glenn, K; Graves, B; Higgins, B; Janson, C; Jiang, N; Liu, JJ; Packman, K; Podlaski, F; Ross, TM; Tovar, C; Vassilev, LT; Zhang, J; Zhang, Z | 1 |
Adames, V; Filipovic, Z; Garrido, R; Glenn, K; Heimbrook, D; Higgins, B; Hussain, S; Kolinsky, K; Lee, E; Linn, M; Meille, C; Packman, K; Tannu, S; Tovar, C; Vassilev, L; Walz, A | 1 |
Berry, P; Chen, L; Del Bello, F; Halliday, GC; Lunec, J; Middleton, SA; Newell, DR; Nichols, GL; Piergentili, A; Rousseau, RF; Tweddle, DA; Zhao, Y | 1 |
Bartkovitz, D; Chu, XJ; Ding, Q; Filipovic, ZM; Glenn, K; Graves, B; Higgins, B; Janson, C; Jiang, N; Liu, JJ; Luk, KC; Packman, K; Tovar, C; Vassilev, LT; Zhang, J; Zhang, Z | 1 |
Bondra, K; Chronowski, C; Houghton, PJ; Kurmasheva, RT; Leasure, J; Middleton, S; Mo, X; Phelps, D; Seum, S; Wang, D | 1 |
Chen, L; Lunec, J; Middleton, SA; Newell, DR; Nichols, GL; Rousseau, RF; Tweddle, DA | 1 |
Golding, BT; Hardcastle, IR; Zhang, B | 1 |
Allo, G; Hai, J; Ludkovski, O; Ng, C; Sakashita, S; Shepherd, FA; Tsao, MS | 1 |
Chaire, V; Chibon, F; Coindre, JM; Hostein, I; Italiano, A; Lagarde, P; Laroche, A; Lesluyes, T; Lucchesi, C; Neuville, A; Tran-Cong, K | 1 |
Kim, ES; Shohet, JM | 1 |
Fretland, AJ; Glenn, KJ; Hussain, S; Palacios, M; Parrott, N; Reddy, MB; Tuerck, D; Vazvaei, F; Yu, LJ; Zhi, J | 1 |
Esfandiari, A; Hawthorne, TA; Lunec, J; Nakjang, S | 1 |
Assouline, S; Blotner, S; Chen, G; Chen, LC; Dickinson, MJ; Drummond, M; Hashemyan, M; Jukofsky, L; Kasner, M; Kelly, KR; Lee, JH; Martinelli, G; Middleton, SA; Nichols, G; Pierceall, WE; Reis, B; Rueger, R; Seiter, K; So, WV; Theron, M; Vey, N; Yee, K; Yoon, SS; Zhong, H | 1 |
Bacac, M; Dangl, M; Friess, T; Herter, S; Herting, F; Klein, C; Muth, G; Sulcova, J; Umana, P | 1 |
Edmondson, RJ; Lunec, J; Zanjirband, M | 1 |
Birzele, F; Dangl, M; Friess, T; Kiialainen, A; Lehmann, C | 1 |
Algeo, MP; Chaire, V; Derieppe, MA; Italiano, A; Laroche-Clary, A; Loarer, FL | 1 |
Gonelli, A; Secchiero, P; Tisato, V; Voltan, R; Zauli, G | 1 |
Aviles-Padilla, K; Barbieri, E; Chakraborty, R; Chen, Z; Kim, ES; Lakoma, A; Molenaar, JJ; Moreno-Smith, M; Nikzad, R; Paust, S; Schild, L; Scorsone, KA; Sheehan, V; Shohet, JM; Tao, L; Vasudevan, SA; Zhang, Y | 1 |
Friess, T; Herting, F; Klein, C; Middleton, S; Umaña, P | 1 |
Andrew Johnson, C; Ayers, GD; Chen, SC; Cobb, P; Flaherty, D; Higgins, B; Johnson, DB; Johnston, JN; Kelley, MC; Malikayil, K; Raman, D; Richmond, A; Saleh, N; Vara, BA; Vilgelm, AE | 1 |
Andreeff, M; Konopleva, M; Leverson, JD; Mu, H; Nichols, G; Pan, R; Reed, JC; Ruvolo, V | 1 |
Aptullahoglu, E; Esfandiari, A; Ho, YH; Lovat, P; Lunec, J; Mahdi, AK; Wang, N; Wu, CE | 1 |
Blotner, S; Chen, LC; Ejadi, S; Miller, W; Nemunaitis, J; Nichols, G; Razak, A; Vazvaei, F; Young, A; Zhi, J | 1 |
Blotner, S; Chen, LC; Ferlini, C; Zhi, J | 1 |
Chen, L; Esfandiari, A; Hogarty, MD; Lunec, J; Reaves, W; Tweddle, DA; Vu, A | 1 |
Chang, Y; Ding, K; Guo, H; Hao, P; Li, L; Li, Z; Ni, Y; Xu, Y; Zhang, ZM; Zhu, D | 1 |
Castro, J; Heam, K; Heightman, TD; Lebraud, H; Lunec, J; Newell, DR; Noble, RA; Phillips, N; Wedge, SR; Zhao, Y | 1 |
Diodone, R; Fishlock, D; Hildbrand, S; Kuhn, B; Mössner, C; Peters, C; Rege, PD; Rimmler, G; Schantz, M | 1 |
Bendszus, M; Berberich, A; Breckwoldt, MO; Ciprut, S; Fischer, M; Hielscher, T; Hucke, N; Kessler, T; Lemke, D; Oezen, I; Platten, M; Pusch, S; Ruebmann, P; Sahm, F; Schmitt, LM; Thomé, CM; von Deimling, A; Wick, W | 1 |
Feringa, BL; Feringa, FM; Hansen, MJ; Kobauri, P; Medema, RH; Szymanski, W | 1 |
Ou Yang, TH; So, WV; Yang, X; Zhi, J | 1 |
Berry, P; Bonner, J; Chen, L; Daga, A; Kirk, C; Lunec, J; Newell, DR; Pastorino, F; Ponzoni, M; Thomas, HD; Tweddle, DA; Veal, GJ; Wood, KM; Zhao, Y | 1 |
Foucar, CE; Stein, BL | 1 |
Natarajan, U; Radhakrishnan, V; Rathinavelu, A; Samuel, S; Venkatesan, T | 1 |
Natarajan, U; Radhakrishnan, V; Rasappan, P; Rathinavelu, A; Samuel, S; Venkatesan, T | 1 |
Blotner, S; Chen, LC; Da Costa, D; Gleave, M; Jones, R; Pápai, Z; Vazvaei, F; Zhi, J | 1 |
Estey, EH; Percival, MM | 1 |
Ritchie, EK | 1 |
Chen, D; Chen, K; Guan, G; Hu, H; Li, G; Li, W; Qiao, M; Qiu, L; Xin, X; Zhao, X | 1 |
Abdul Razak, AR; Blotner, S; Chen, LC; Gore, L; Higgins, B; Miller, WH; Uy, GL; Young, AM | 1 |
Assouline, S; Blotner, S; Chen, LC; Higgins, B; Uy, GL; Yee, K; Young, AM | 1 |
Corbali, MO; Eskazan, AE | 1 |
Crown, J; Duffy, MJ; O'Grady, S; Synnott, NC | 1 |
Cui, Y; Rong, F; Zhou, J | 1 |
Arango Ossa, JE; Cassinat, B; Dueck, A; Farnoud, N; Hoffman, R; Houldsworth, J; Kiladjian, JJ; Kosiorek, H; Levine, MF; Lu, M; Marcellino, BK; Mascarenhas, J; McGovern, E; Medina-Martinez, J; Mehrotra, M; Patel, M; Rampal, RK; Rossi, M; Verger, E; Zhou, Y | 1 |
Assouline, S; Blotner, S; Chen, LC; Dickinson, MJ; Drummond, MW; Higgins, B; Jukofsky, L; Kasner, M; Kelly, KR; Lee, JH; Martinelli, G; Monnet, A; Muehlbauer, S; Nichols, G; Ott, M; Papayannidis, C; Pierceall, WE; Seiter, K; Simon, S; Vey, N; Yee, K; Yoon, SS; Zhi, J | 1 |
Alles, LK; Bate-Eya, LT; Dolman, MEM; Egan, DA; Goldsmith, KC; Jonus, HC; Kerstjens, M; Koopmans, B; Koster, J; Lee, JY; Lelieveld, D; Molenaar, JJ; Schild, L; Schubert, NA; Stam, RW; Vernooij, L | 1 |
Ayyagari, P; Das, SK; Pollok, KE; Shannon, HE; Smiley, SB; Vannier, MW; Veronesi, MC; Yun, Y | 1 |
Abdeldayem, A; Aittokallio, T; Bhatti, MN; Bukhari, S; de Araujo, ED; Gawel, JM; Geletu, M; Gunning, PT; Hassan, MM; Herling, M; Ianevski, A; Israelian, J; Krämer, OH; Manaswiyoungkul, P; Moriggl, R; Mustjoki, S; Nawar, N; Neubauer, HA; Olaoye, OO; Radu, TB; Raouf, YS; Sedighi, A; Shouksmith, AE; Sorger, H; Timonen, S; Toutah, K; von Jan, J | 1 |
Bang, YJ; Blay, JY; Blotner, S; Chen, LC; Gietema, JA; Higgins, B; Hirte, HW; Italiano, A; Jamois, C; Mileshkin, LR; Miller, WH; Nichols, GL; Petry, C; Schmitt, C; Siu, LL; Yang, QJ | 1 |
Chen, LH; Diplas, BH; Greer, PK; He, Y; Liu, H; Pirozzi, CJ; Waitkus, MS; Xu, C; Yan, H; Zhang, L | 1 |
Bellini, M; Burbury, K; El-Galaly, TC; Gerds, A; Gupta, V; Higgins, B; Huw, LY; Jamois, C; Katakam, S; Kovic, B; Maffioli, M; Mascarenhas, J; Mesa, R; Palmer, J; Passamonti, F; Ross, DM; Vannucchi, AM; Wonde, K; Yacoub, A | 1 |
Cleary, Y; Fowler, S; Parrott, N; Tuerck, D; Umehara, K | 1 |
Beckermann, BM; Catalani, O; Cavenagh, J; Deeren, D; Fenaux, P; Genevray, M; Girshova, L; Jamois, C; Konopleva, MY; Krauter, J; Martinelli, G; Montesinos, P; Muehlbauer, S; Mundt, K; Ott, M; Ottmann, O; Petrini, M; Pigneux, A; Rambaldi, A; Recher, C; Rodriguez-Veiga, R; Röllig, C; Schäfer, JA; Taussig, D; Vey, N; Wei, AH; Yoon, SS | 1 |
5 review(s) available for 4-aminobenzoic acid and rg7388
Article | Year |
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Small-molecule MDM2-p53 inhibitors: recent advances.
Topics: Animals; Antineoplastic Agents; Clinical Trials as Topic; Crystallography, X-Ray; Humans; Imidazoles; Indoles; Models, Molecular; Neoplasms; Oxindoles; para-Aminobenzoates; Piperazines; Protein Interaction Maps; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Small Molecule Libraries; Structure-Activity Relationship; Tumor Suppressor Protein p53 | 2015 |
MDM2/X inhibitors under clinical evaluation: perspectives for the management of hematological malignancies and pediatric cancer.
Topics: Animals; Antineoplastic Agents; Cell Cycle Proteins; Child; Hematologic Neoplasms; Humans; Imidazolines; Indoles; Molecular Targeted Therapy; Nuclear Proteins; para-Aminobenzoates; Protein Interaction Maps; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Signal Transduction; Spiro Compounds; Tumor Suppressor Protein p53 | 2017 |
Novel therapeutic approaches in polycythemia vera.
Topics: Clinical Trials, Phase II as Topic; Clinical Trials, Phase III as Topic; Half-Life; Humans; Hydroxyurea; Interferon alpha-2; Interferon-alpha; Nitriles; para-Aminobenzoates; Polycythemia Vera; Polyethylene Glycols; Pyrazoles; Pyrimidines; Pyrrolidines; Recombinant Proteins; Salvage Therapy | 2018 |
Current treatment strategies for measurable residual disease in patients with acute myeloid leukemia.
Topics: Aminopyridines; Aniline Compounds; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Antineoplastic Agents, Immunological; Azacitidine; Cytogenetic Analysis; Decitabine; Enzyme Inhibitors; Flow Cytometry; Hematopoietic Stem Cell Transplantation; Humans; Hydrazines; Immunologic Factors; In Situ Hybridization, Fluorescence; Lenalidomide; Leukemia, Myeloid, Acute; Molecular Diagnostic Techniques; Neoplasm, Residual; Nivolumab; para-Aminobenzoates; Protein Kinase Inhibitors; Pyrazines; Pyrrolidines; Recombinant Fusion Proteins; Remission Induction; Transplantation, Homologous; Triazines; Triazoles | 2019 |
Targeting p53 for the treatment of cancer.
Topics: Aminoquinolines; Antineoplastic Agents; Cell Cycle Proteins; Humans; Neoplasms; para-Aminobenzoates; Protein Isoforms; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Quinuclidines; Thiosemicarbazones; Tumor Suppressor Protein p53 | 2022 |
9 trial(s) available for 4-aminobenzoic acid and rg7388
Article | Year |
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Acute myeloid leukemia patients' clinical response to idasanutlin (RG7388) is associated with pre-treatment MDM2 protein expression in leukemic blasts.
Topics: Blast Crisis; Female; Gene Expression Regulation, Leukemic; Humans; Leukemia, Myeloid, Acute; Male; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines | 2016 |
Phase 1 summary of plasma concentration-QTc analysis for idasanutlin, an MDM2 antagonist, in patients with advanced solid tumors and AML.
Topics: Acute Disease; Adult; Aged; Aged, 80 and over; Dose-Response Relationship, Drug; Electrocardiography; Female; Heart Rate; Humans; Leukemia, Myeloid; Long QT Syndrome; Male; Middle Aged; Neoplasms; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Young Adult | 2018 |
A single-center, open-label study investigating the excretion balance, pharmacokinetics, metabolism, and absolute bioavailability of a single oral dose of [
Topics: Administration, Oral; Adult; Aged; Antineoplastic Agents; Biological Availability; Cohort Studies; Drug Interactions; Female; Humans; Male; Middle Aged; Neoplasms; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines | 2019 |
A phase 1 study of the MDM2 antagonist RO6839921, a pegylated prodrug of idasanutlin, in patients with advanced solid tumors.
Topics: Administration, Oral; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Female; Growth Differentiation Factor 15; Humans; Infusions, Intravenous; Male; Middle Aged; Neoplasms; para-Aminobenzoates; Polyethylene Glycols; Prodrugs; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Treatment Outcome; Tumor Suppressor Protein p53 | 2020 |
Phase 1 study of the MDM2 antagonist RO6839921 in patients with acute myeloid leukemia.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Female; Humans; Infusions, Intravenous; Leukemia, Myeloid, Acute; Male; Maximum Tolerated Dose; Middle Aged; para-Aminobenzoates; Prodrugs; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Young Adult | 2020 |
Murine double minute 2 inhibition alone or with cytarabine in acute myeloid leukemia: Results from an idasanutlin phase 1/1b study⋆.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Cytarabine; Female; Follow-Up Studies; Humans; Leukemia, Myeloid, Acute; Male; Maximum Tolerated Dose; Middle Aged; para-Aminobenzoates; Prognosis; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Remission Induction; Tissue Distribution; Young Adult | 2021 |
Phase I study of daily and weekly regimens of the orally administered MDM2 antagonist idasanutlin in patients with advanced tumors.
Topics: Adult; Aged; Antineoplastic Agents; Dose-Response Relationship, Drug; Drug Administration Schedule; Female; Humans; Male; Maximum Tolerated Dose; Middle Aged; Neoplasms; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines | 2021 |
The MDM2 antagonist idasanutlin in patients with polycythemia vera: results from a single-arm phase 2 study.
Topics: Humans; Hydroxyurea; Nausea; para-Aminobenzoates; Polycythemia Vera; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Splenomegaly; Vomiting | 2022 |
Idasanutlin plus cytarabine in relapsed or refractory acute myeloid leukemia: results of the MIRROS trial.
Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Cytarabine; Humans; Leukemia, Myeloid, Acute; para-Aminobenzoates; Pyrrolidines | 2022 |
41 other study(ies) available for 4-aminobenzoic acid and rg7388
Article | Year |
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Discovery of RG7388, a potent and selective p53-MDM2 inhibitor in clinical development.
Topics: Animals; Antineoplastic Agents; Drug Discovery; Humans; Male; Mice; Mice, Inbred C57BL; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53 | 2013 |
Preclinical optimization of MDM2 antagonist scheduling for cancer treatment by using a model-based approach.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Apoptosis; Bone Neoplasms; Cell Line, Tumor; Drug Administration Schedule; Female; Humans; Imidazolines; Mice, Nude; Osteosarcoma; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Xenograft Model Antitumor Assays | 2014 |
Structurally diverse MDM2-p53 antagonists act as modulators of MDR-1 function in neuroblastoma.
Topics: Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 1; Cell Line, Tumor; Cisplatin; Doxorubicin; Drug Resistance, Neoplasm; Drug Synergism; Humans; Imidazoles; Indoles; Inhibitory Concentration 50; Neuroblastoma; para-Aminobenzoates; Piperazines; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Spiro Compounds; Tumor Suppressor Protein p53; Verapamil; Vincristine | 2014 |
Discovery of potent and selective spiroindolinone MDM2 inhibitor, RO8994, for cancer therapy.
Topics: Apoptosis; Binding Sites; Cell Line, Tumor; Cell Proliferation; Drug Evaluation, Preclinical; Humans; Imidazolines; Indoles; Indolizidines; Molecular Dynamics Simulation; Neoplasms; para-Aminobenzoates; Protein Binding; Protein Structure, Tertiary; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Spiro Compounds; Tumor Suppressor Protein p53 | 2014 |
Inhibition of MDM2 by RG7388 confers hypersensitivity to X-radiation in xenograft models of childhood sarcoma.
Topics: Animals; Apoptosis; Apoptosis Regulatory Proteins; Child; Child, Preschool; Cyclin-Dependent Kinase Inhibitor p21; DNA-Binding Proteins; Female; Growth Differentiation Factor 15; Humans; Mice; Mice, Nude; Neoplasm Recurrence, Local; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Radiation-Sensitizing Agents; Rhabdomyosarcoma; Tumor Suppressor Protein p53; Tumor Suppressor Proteins; Xenograft Model Antitumor Assays | 2015 |
Pre-clinical evaluation of the MDM2-p53 antagonist RG7388 alone and in combination with chemotherapy in neuroblastoma.
Topics: Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Cell Line, Tumor; Drug Screening Assays, Antitumor; Humans; Neuroblastoma; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53 | 2015 |
Inhibiting MDM2-p53 Interaction Suppresses Tumor Growth in Patient-Derived Non-Small Cell Lung Cancer Xenograft Models.
Topics: Animals; Antineoplastic Agents; Apoptosis; Carcinoma, Non-Small-Cell Lung; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Humans; Lung Neoplasms; Mice; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Sequence Analysis, DNA; Signal Transduction; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2015 |
Heterogeneous Mechanisms of Secondary Resistance and Clonal Selection in Sarcoma during Treatment with Nutlin.
Topics: Antineoplastic Agents; Apoptosis; Autophagy; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Clone Cells; Drug Resistance, Neoplasm; Gene Expression Profiling; Humans; Imidazoles; Mutation; para-Aminobenzoates; Ploidies; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Sarcoma; Sequence Analysis, RNA; Signal Transduction; Tumor Suppressor Protein p53 | 2015 |
Reactivation of p53 via MDM2 inhibition.
Topics: Animals; Apoptosis; Cell Line, Tumor; Hypoxia-Inducible Factor 1, alpha Subunit; Mice; Neovascularization, Pathologic; Neuroblastoma; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53; Vascular Endothelial Growth Factor A | 2015 |
Investigating the effect of autoinduction in cynomolgus monkeys of a novel anticancer MDM2 antagonist, idasanutlin, and relevance to humans.
Topics: Animals; Antineoplastic Agents; Humans; Macaca fascicularis; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines | 2016 |
Chemical Inhibition of Wild-Type p53-Induced Phosphatase 1 (WIP1/PPM1D) by GSK2830371 Potentiates the Sensitivity to MDM2 Inhibitors in a p53-Dependent Manner.
Topics: Aminopyridines; Antineoplastic Agents; Apoptosis; Caspase 3; Caspase 7; Catalysis; Cell Line, Tumor; Cell Survival; Dipeptides; Dose-Response Relationship, Drug; Drug Resistance, Neoplasm; Drug Synergism; Humans; Imidazoles; Mutation; Neoplasms; para-Aminobenzoates; Piperazines; Protein Phosphatase 2C; Proteolysis; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Transcription, Genetic; Tumor Suppressor Protein p53; Ubiquitin | 2016 |
Antitumour activity of the glycoengineered type II anti-CD20 antibody obinutuzumab (GA101) in combination with the MDM2-selective antagonist idasanutlin (RG7388).
Topics: Animals; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antibody-Dependent Cell Cytotoxicity; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Disease Models, Animal; Dose-Response Relationship, Drug; Humans; Killer Cells, Natural; Lymphocyte Depletion; Lymphoma, B-Cell; Mice; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Burden; Xenograft Model Antitumor Assays | 2016 |
Pre-clinical efficacy and synergistic potential of the MDM2-p53 antagonists, Nutlin-3 and RG7388, as single agents and in combined treatment with cisplatin in ovarian cancer.
Topics: Apoptosis; Cell Cycle; Cell Line, Tumor; Cell Survival; Cisplatin; DNA Repair; Female; Gene Expression Regulation, Neoplastic; Genotype; Humans; Imidazoles; Ovarian Neoplasms; para-Aminobenzoates; Piperazines; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53 | 2016 |
Superior anti-tumor activity of the MDM2 antagonist idasanutlin and the Bcl-2 inhibitor venetoclax in p53 wild-type acute myeloid leukemia models.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Bridged Bicyclo Compounds, Heterocyclic; Cell Cycle; Cell Line, Tumor; Cell Survival; Drug Synergism; Female; Gene Expression Profiling; Heterografts; Humans; Leukemia, Myeloid, Acute; Mice; Myeloid Cell Leukemia Sequence 1 Protein; para-Aminobenzoates; Proto-Oncogene Proteins c-bcl-2; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Sequence Analysis, RNA; Sulfonamides; Tumor Suppressor Protein p53 | 2016 |
Combined targeting of MDM2 and CDK4 is synergistic in dedifferentiated liposarcomas.
Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinase 4; Drug Synergism; Female; Humans; Liposarcoma; Mice; Molecular Targeted Therapy; para-Aminobenzoates; Piperazines; Proto-Oncogene Proteins c-mdm2; Pyridines; Pyrrolidines | 2017 |
p53 Nongenotoxic Activation and mTORC1 Inhibition Lead to Effective Combination for Neuroblastoma Therapy.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Cell Line, Tumor; Cell Proliferation; Drug Resistance, Neoplasm; Gene Expression Regulation, Neoplastic; Humans; Mechanistic Target of Rapamycin Complex 1; Mice; Neuroblastoma; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Sirolimus; TOR Serine-Threonine Kinases; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2017 |
Chemotherapy-free, triple combination of obinutuzumab, venetoclax and idasanutlin: antitumor activity in xenograft models of non-Hodgkin lymphoma.
Topics: Animals; Antibodies, Monoclonal, Humanized; Bridged Bicyclo Compounds, Heterocyclic; Disease Models, Animal; Drug Therapy, Combination; Humans; Lymphoma, Non-Hodgkin; Mice; para-Aminobenzoates; Pyrrolidines; Sulfonamides; Xenograft Model Antitumor Assays | 2018 |
MDM2 Antagonists Counteract Drug-Induced DNA Damage.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Azepines; Cell Line, Tumor; Cyclin-Dependent Kinase Inhibitor p21; DNA Damage; DNA Replication; HCT116 Cells; Humans; Imidazoles; Melanoma; Mice; para-Aminobenzoates; Piperazines; Protein Binding; Proto-Oncogene Proteins c-mdm2; Pyrimidines; Pyrrolidines; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2017 |
Synthetic Lethality of Combined Bcl-2 Inhibition and p53 Activation in AML: Mechanisms and Superior Antileukemic Efficacy.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Bridged Bicyclo Compounds, Heterocyclic; Cell Line, Tumor; Drug Resistance, Neoplasm; Female; Humans; Leukemia, Myeloid, Acute; Mice; Mice, Inbred NOD; Mice, SCID; para-Aminobenzoates; Proto-Oncogene Proteins c-bcl-2; Pyrrolidines; Sulfonamides; Synthetic Lethal Mutations; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2017 |
Targeting negative regulation of p53 by MDM2 and WIP1 as a therapeutic strategy in cutaneous melanoma.
Topics: Aminopyridines; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Cell Survival; Dipeptides; Drug Synergism; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Humans; Imidazoles; Melanoma; Melanoma, Cutaneous Malignant; Mutagenesis, Site-Directed; para-Aminobenzoates; Phosphorylation; Piperazines; Protein Binding; Protein Phosphatase 2C; Protein Stability; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Skin Neoplasms; Tumor Suppressor Protein p53 | 2018 |
Effects of posaconazole (a strong CYP3A4 inhibitor), two new tablet formulations, and food on the pharmacokinetics of idasanutlin, an MDM2 antagonist, in patients with advanced solid tumors.
Topics: Administration, Oral; Area Under Curve; Biological Availability; Cross-Over Studies; Cytochrome P-450 CYP3A Inhibitors; Drug Compounding; Drug Interactions; Fasting; Female; Food-Drug Interactions; Humans; Male; Middle Aged; Neoplasm Staging; Neoplasms; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tablets; Therapeutic Equivalency; Triazoles | 2018 |
Characterisation of the p53 pathway in cell lines established from TH-MYCN transgenic mouse tumours.
Topics: Animals; Cell Line, Tumor; Disease Models, Animal; Humans; Imidazoles; Indoles; Mice; Mice, Transgenic; Mutation; N-Myc Proto-Oncogene Protein; Neuroblastoma; para-Aminobenzoates; Piperazines; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Radiation, Ionizing; Signal Transduction; Spiro Compounds; Tumor Suppressor Protein p53 | 2018 |
Cell- and Tissue-Based Proteome Profiling and Dual Imaging of Apoptosis Markers with Probes Derived from Venetoclax and Idasanutlin.
Topics: Antineoplastic Agents; Apoptosis; Biomarkers, Tumor; Breast Neoplasms; Bridged Bicyclo Compounds, Heterocyclic; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Fluorescent Dyes; Humans; MCF-7 Cells; Models, Molecular; Molecular Structure; Optical Imaging; para-Aminobenzoates; Proteome; Proto-Oncogene Proteins c-bcl-2; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Structure-Activity Relationship; Sulfonamides | 2018 |
Highly Potent Clickable Probe for Cellular Imaging of MDM2 and Assessing Dynamic Responses to MDM2-p53 Inhibition.
Topics: Boron Compounds; Cell Line, Tumor; Click Chemistry; Cyclooctanes; Fluorescent Dyes; Humans; Molecular Docking Simulation; Optical Imaging; para-Aminobenzoates; Protein Binding; Protein Interaction Maps; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53 | 2018 |
Efficient Industrial Synthesis of the MDM2 Antagonist Idasanutlin via a Cu(I)-catalyzed [3+2] Asymmetric Cycloaddition.
Topics: Catalysis; Copper; Cycloaddition Reaction; Hydrolysis; Isomerism; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines | 2018 |
Targeting Resistance against the MDM2 Inhibitor RG7388 in Glioblastoma Cells by the MEK Inhibitor Trametinib.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Cell Line, Tumor; Drug Resistance, Neoplasm; Glioblastoma; Heterografts; Humans; Insulin-Like Growth Factor Binding Protein 1; Mice; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyridones; Pyrimidinones; Pyrrolidines; Signal Transduction; Tumor Suppressor Protein p53 | 2019 |
Photoactivation of MDM2 Inhibitors: Controlling Protein-Protein Interaction with Light.
Topics: Animals; Cell Line, Tumor; Coumarins; Humans; Light; Molecular Docking Simulation; para-Aminobenzoates; Protein Binding; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Transcription Factors; Xenopus laevis; Xenopus Proteins | 2018 |
Lack of UGT polymorphism association with idasanutlin pharmacokinetics in solid tumor patients.
Topics: Glucuronosyltransferase; Humans; Neoplasms; para-Aminobenzoates; Polymorphism, Single Nucleotide; Prognosis; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tissue Distribution | 2019 |
Preclinical evaluation of the first intravenous small molecule MDM2 antagonist alone and in combination with temozolomide in neuroblastoma.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Drug Screening Assays, Antitumor; Drug Synergism; Humans; Mice; Neuroblastoma; para-Aminobenzoates; Prodrugs; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Random Allocation; Temozolomide; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2019 |
Differential Mechanisms of Cell Death Induced by HDAC Inhibitor SAHA and MDM2 Inhibitor RG7388 in MCF-7 Cells.
Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; bcl-2-Associated X Protein; Cell Cycle Checkpoints; Cell Death; Cyclin-Dependent Kinase Inhibitor p21; Female; Histone Deacetylase Inhibitors; Humans; Letrozole; MCF-7 Cells; para-Aminobenzoates; Protein Kinases; Pyrrolidines; Receptor-Interacting Protein Serine-Threonine Kinases; Vorinostat | 2018 |
Cell Cycle Arrest and Cytotoxic Effects of SAHA and RG7388 Mediated through p21
Topics: Apoptosis; Breast Neoplasms; Cell Cycle Checkpoints; Cell Survival; Cyclin-Dependent Kinase Inhibitor p21; Cyclin-Dependent Kinase Inhibitor p27; Drug Discovery; Female; Histone Deacetylase Inhibitors; Humans; Male; MCF-7 Cells; para-Aminobenzoates; Prostatic Neoplasms; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53; Vorinostat | 2019 |
Drug development challenges in polycythemia vera.
Topics: Drug Development; Humans; para-Aminobenzoates; Polycythemia Vera; Pyrrolidines | 2019 |
Co-delivery of p53 and MDM2 inhibitor RG7388 using a hydroxyl terminal PAMAM dendrimer derivative for synergistic cancer therapy.
Topics: Animals; Apoptosis; Biomarkers, Tumor; Body Weight; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Movement; Cell Proliferation; Dendrimers; Drug Liberation; Female; Gene Transfer Techniques; Human Umbilical Vein Endothelial Cells; Humans; Mice, Inbred BALB C; Mice, Nude; Neoplasm Invasiveness; Neoplasms; Neovascularization, Physiologic; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53 | 2019 |
Idasanutlin as a new treatment option in improving the therapeutic odyssey of relapsed/refractory AML.
Topics: Antineoplastic Agents; Biomarkers, Tumor; Drug Resistance, Neoplasm; Humans; Leukemia, Myeloid, Acute; para-Aminobenzoates; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Recurrence; Retreatment; Treatment Outcome | 2020 |
Combination of metformin and RG7388 enhances inhibition of growth and induction of apoptosis of ovarian cancer cells through the PI3K/AKT/mTOR pathway.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Cell Line, Tumor; Cell Proliferation; Female; Humans; MAP Kinase Signaling System; Metformin; Mice, Nude; Ovarian Neoplasms; para-Aminobenzoates; Phosphatidylinositol 3-Kinase; Proto-Oncogene Proteins c-akt; Pyrrolidines; Reactive Oxygen Species; TOR Serine-Threonine Kinases; Xenograft Model Antitumor Assays | 2020 |
Transient expansion of TP53 mutated clones in polycythemia vera patients treated with idasanutlin.
Topics: Clone Cells; Humans; para-Aminobenzoates; Polycythemia Vera; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53 | 2020 |
High-Throughput Screening Identifies Idasanutlin as a Resensitizing Drug for Venetoclax-Resistant Neuroblastoma Cells.
Topics: Animals; Cell Line, Tumor; Disease Models, Animal; High-Throughput Screening Assays; Humans; Mice; Neuroblastoma; para-Aminobenzoates; Proto-Oncogene Proteins c-mdm2; Pyrrolidines | 2021 |
Development of CD133 Targeting Multi-Drug Polymer Micellar Nanoparticles for Glioblastoma - In Vitro Evaluation in Glioblastoma Stem Cells.
Topics: AC133 Antigen; Animals; Brain Neoplasms; Cell Line, Tumor; Dose-Response Relationship, Drug; Drug Delivery Systems; Drug Development; Drug Evaluation, Preclinical; Glioblastoma; Humans; Mice; Micelles; Nanoparticles; Neoplastic Stem Cells; para-Aminobenzoates; Polymers; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Temozolomide | 2021 |
Development of HDAC Inhibitors Exhibiting Therapeutic Potential in T-Cell Prolymphocytic Leukemia.
Topics: Animals; Antineoplastic Agents; Apoptosis; Bendamustine Hydrochloride; Bridged Bicyclo Compounds, Heterocyclic; Cell Line, Tumor; Drug Synergism; Histone Deacetylase 6; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Leukemia, Prolymphocytic, T-Cell; Male; Mice; Molecular Docking Simulation; Molecular Structure; para-Aminobenzoates; Pyrrolidines; Structure-Activity Relationship; Sulfonamides | 2021 |
TP53 wild-type/PPM1D mutant diffuse intrinsic pontine gliomas are sensitive to a MDM2 antagonist.
Topics: Animals; Antineoplastic Agents; Apoptosis; Brain Stem Neoplasms; Cell Line, Tumor; Cell Proliferation; Cell Survival; Diffuse Intrinsic Pontine Glioma; Humans; Mice; para-Aminobenzoates; Protein Phosphatase 2C; Proto-Oncogene Proteins c-mdm2; Pyrrolidines; Tumor Suppressor Protein p53; Xenograft Model Antitumor Assays | 2021 |
Accelerating Clinical Development of Idasanutlin through a Physiologically Based Pharmacokinetic Modeling Risk Assessment for CYP450 Isoenzyme-Related Drug-Drug Interactions.
Topics: Cytochrome P-450 CYP3A; Cytochrome P-450 CYP3A Inhibitors; Drug Interactions; Humans; Isoenzymes; Leukemia, Myeloid, Acute; Models, Biological; para-Aminobenzoates; Pyrrolidines; Risk Assessment | 2022 |