celecoxib has been researched along with Cancer of Colon in 119 studies
Excerpt | Relevance | Reference |
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"Celecoxib is approved as an adjunctive chemopreventive agent in adults with familial adenomatous polyposis (FAP)." | 9.14 | The safety and efficacy of celecoxib in children with familial adenomatous polyposis. ( Ayers, GD; Burke, CA; Church, J; Eagle, C; Half, E; Hasson, H; Hawk, E; Lynch, PM; Patterson, S; Richmond, E; Woloj, M, 2010) |
"This study was designated to explore the role of cancer stem cells (CSCs) during chemically induced mouse colon carcinogenesis (by 1,2- dimethylhydrazine dihydrochloride, DMH) with/or without the treatment with a targeted (anti-COX-2) therapeutic drug, celecoxib." | 7.91 | Celecoxib Targeted Therapy Attenuates Mouse Colon Carcinogenesis through Modulation of Expression Patterns of Cancer Stem Cells. ( Eltonouby, EA; Hegazi, MM; Helmy, HM; Kang, JS; Mahfouz, ME; Salim, EI, 2019) |
"The purpose of this study was to investigate the role of colon cancer stem cells (CSCs) during chemicallyinduced rat multi-step colon carcinogenesis with or without the treatment with a specific cyclooxygenase-2 inhibitor drug (celecoxib)." | 7.83 | Expression Patterns of Cancer Stem Cell Markers During Specific Celecoxib Therapy in Multistep Rat Colon Carcinogenesis Bioassays. ( Hegazi, MM; Helmy, HM; Kang, JS; Salim, EI, 2016) |
"This study was performed to evaluate whether down-regulation of prostaglandin E(2) (PGE(2)) synthesis by celecoxib treatment is associated with inhibition of cell growth in human colon carcinoma cell lines." | 7.74 | Down-regulation of PGE2 by physiologic levels of celecoxib is not sufficient to induce apoptosis or inhibit cell proliferation in human colon carcinoma cell lines. ( Arber, N; Ben-Yosef, R; Kazanov, D; Lev-Ari, S; Liberman, E, 2007) |
"Celecoxib has proven to be a very prominent member of this group with cytostatic activities." | 5.51 | Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines. ( Buzharevski, A; Hey-Hawkins, E; Laube, M; Lönnecke, P; Maksimovic-Ivanic, D; Mijatovic, S; Neumann, W; Paskas, S; Pietzsch, J; Sárosi, MB, 2019) |
"Local recurrence in colon cancer causes poor prognosis affecting overall survival of cancer-affected patient population." | 5.43 | Cooperative effect of BI-69A11 and celecoxib enhances radiosensitization by modulating DNA damage repair in colon carcinoma. ( Chaurasia, M; Chowdhury, T; Das, S; Dey, KK; Mandal, M; Pal, I; Parida, S; Rajesh, Y; Sharma, K, 2016) |
"HT-29 colon cancer cells and LT97 colorectal micro-adenoma cells derived from a patient with FAP, were exposed to low dose celecoxib and UDCA alone or in combination with tauro-cholic acid (CA) and tauro-chenodeoxycholic acid (CDCA), mimicking bile of FAP patients treated with UDCA." | 5.38 | Celecoxib and tauro-ursodeoxycholic acid co-treatment inhibits cell growth in familial adenomatous polyposis derived LT97 colon adenoma cells. ( Marian, B; Nagengast, FM; Peters, WH; Roelofs, HM; Te Morsche, RH; van Heumen, BW, 2012) |
"Celecoxib is approved as an adjunctive chemopreventive agent in adults with familial adenomatous polyposis (FAP)." | 5.14 | The safety and efficacy of celecoxib in children with familial adenomatous polyposis. ( Ayers, GD; Burke, CA; Church, J; Eagle, C; Half, E; Hasson, H; Hawk, E; Lynch, PM; Patterson, S; Richmond, E; Woloj, M, 2010) |
"NSAIDs such as celecoxib and sulindac play a critical role in the treatment of colorectal cancer, yet it is not understood how sufficiently high concentrations are reached in colonic tissue." | 4.02 | Insight into the Colonic Disposition of Sulindac in Humans. ( Augustijns, P; Brouwers, J; Lemmens, G; Snoeys, J; Vanuytsel, T, 2021) |
"This study was designated to explore the role of cancer stem cells (CSCs) during chemically induced mouse colon carcinogenesis (by 1,2- dimethylhydrazine dihydrochloride, DMH) with/or without the treatment with a targeted (anti-COX-2) therapeutic drug, celecoxib." | 3.91 | Celecoxib Targeted Therapy Attenuates Mouse Colon Carcinogenesis through Modulation of Expression Patterns of Cancer Stem Cells. ( Eltonouby, EA; Hegazi, MM; Helmy, HM; Kang, JS; Mahfouz, ME; Salim, EI, 2019) |
"The purpose of this study was to investigate the role of colon cancer stem cells (CSCs) during chemicallyinduced rat multi-step colon carcinogenesis with or without the treatment with a specific cyclooxygenase-2 inhibitor drug (celecoxib)." | 3.83 | Expression Patterns of Cancer Stem Cell Markers During Specific Celecoxib Therapy in Multistep Rat Colon Carcinogenesis Bioassays. ( Hegazi, MM; Helmy, HM; Kang, JS; Salim, EI, 2016) |
"Several studies have shown the anti-neoplastic effects of non-steroidal anti-inflammatory drugs (NSAIDs) on 1,2-dimethylhydrazine (DMH)-induced colon carcinogenesis, but how these drugs act in case of inflammation-augmented tumorigenesis is still not clear." | 3.80 | Activation of NF-κB: bridging the gap between inflammation and cancer in colitis-mediated colon carcinogenesis. ( Nehru, B; Sanyal, SN; Setia, S, 2014) |
"The expression of the putative markers LGR-5 (leucine-rich-repeat-containing G-protein-coupled receptor 5), MSI-1 (Musashi-1) and DCAMKL-1 (doublecortin and calcium/calmodulin-dependent protein kinase-like-1) was studied in normal colon mucosa (NM), in the precancerous lesions Mucin Depleted Foci (MDF) and in macroscopic tumours (adenomas) of 1,2-dimethylhydrazine-treated rats." | 3.79 | Expression of LGR-5, MSI-1 and DCAMKL-1, putative stem cell markers, in the early phases of 1,2-dimethylhydrazine-induced rat colon carcinogenesis: correlation with nuclear β-catenin. ( Caderni, G; Dolara, P; Femia, AP; Salvadori, M, 2013) |
"This study was performed to evaluate whether down-regulation of prostaglandin E(2) (PGE(2)) synthesis by celecoxib treatment is associated with inhibition of cell growth in human colon carcinoma cell lines." | 3.74 | Down-regulation of PGE2 by physiologic levels of celecoxib is not sufficient to induce apoptosis or inhibit cell proliferation in human colon carcinoma cell lines. ( Arber, N; Ben-Yosef, R; Kazanov, D; Lev-Ari, S; Liberman, E, 2007) |
"Elevated polyamine and nitric oxide levels (both derived from arginine) promote tumorigenesis, whereas non-steroidal anti-inflammatory drugs (NSAIDs) inhibit colorectal cancer (CRC) incidence in experimental and epidemiologic studies." | 3.74 | Risk and risk reduction involving arginine intake and meat consumption in colorectal tumorigenesis and survival. ( Anton-Culver, H; Besselsen, DG; Gerner, EW; Ignatenko, NA; Yerushalmi, HF; Zell, JA; Ziogas, A, 2007) |
"A total of 2526 patients with stage III colon cancer were enrolled between June 2010 and November 2015 and were followed up through August 10, 2020." | 3.01 | Effect of Celecoxib vs Placebo Added to Standard Adjuvant Therapy on Disease-Free Survival Among Patients With Stage III Colon Cancer: The CALGB/SWOG 80702 (Alliance) Randomized Clinical Trial. ( Bendell, JC; Bertagnolli, M; Blanke, C; Couture, F; Fuchs, CS; Goldberg, RM; Grothey, A; Guthrie, KA; Hochster, HS; Kuebler, P; Kumar, P; Kumthekar, P; Lewis, D; Meyer, J; Meyerhardt, JA; Niedzwiecki, D; O'Reilly, EM; Shi, Q; Shields, AF; Tan, B; Venook, A; Zemla, T, 2021) |
"Celecoxib has been accounted to be an effective antitumor drug, but may exhibit significant side effects." | 1.91 | ADT-OH synergistically enhanced the antitumor activity of celecoxib in human colorectal cancer cells. ( Cai, F; Hua, ZC; Li, P; Ma, H; Sun, H; Tan, Y; Wang, X; Xu, H; Xu, J; Zhuang, H, 2023) |
"PIP as a bioenhancer increased the oral bioavailability of CXB (129%)." | 1.62 | Piperine and Celecoxib synergistically inhibit colon cancer cell proliferation via modulating Wnt/β-catenin signaling pathway. ( Chaturvedi, S; Dewangan, J; Divakar, A; Kumar, S; Mishra, S; Rath, SK; Srivastava, S; Wahajuddin, M, 2021) |
"The fifth case was a breast cancer patient with distant metastases in CR, while receiving beta-interferon and interleukin-2 in addition to conventional hormone therapy." | 1.51 | Treatment of Metastatic or High-Risk Solid Cancer Patients by Targeting the Immune System and/or Tumor Burden: Six Cases Reports. ( Carpi, A; Ferrari, P; Morganti, R; Nicolini, A, 2019) |
"Celecoxib has proven to be a very prominent member of this group with cytostatic activities." | 1.51 | Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines. ( Buzharevski, A; Hey-Hawkins, E; Laube, M; Lönnecke, P; Maksimovic-Ivanic, D; Mijatovic, S; Neumann, W; Paskas, S; Pietzsch, J; Sárosi, MB, 2019) |
"Local recurrence in colon cancer causes poor prognosis affecting overall survival of cancer-affected patient population." | 1.43 | Cooperative effect of BI-69A11 and celecoxib enhances radiosensitization by modulating DNA damage repair in colon carcinoma. ( Chaurasia, M; Chowdhury, T; Das, S; Dey, KK; Mandal, M; Pal, I; Parida, S; Rajesh, Y; Sharma, K, 2016) |
"We used gastric and colon cancer cell lines to study the synergistic effect of As4S4 in combination with BRD4 inhibitor JQ1, or with chemotherapy drug cisplatin and irinotecan or with COX2 inhibitor celecoxib." | 1.42 | Arsenic sulfide combined with JQ1, chemotherapy agents, or celecoxib inhibit gastric and colon cancer cell growth. ( Chen, S; Pan, M; Tong, Y; Zhang, L; Zhang, X, 2015) |
"CD133-positive cancer stem cells in colon cancer are resistant to conventional chemotherapy." | 1.39 | Celecoxib downregulates CD133 expression through inhibition of the Wnt signaling pathway in colon cancer cells. ( Deng, Y; Fu, X; Lin, EH; Mo, J; Su, Q; Zhang, Y, 2013) |
"Celecoxib treatment activated Cdc25C and inhibited p21 expression in both unirradiated and irradiated cells, regardless of COX-2 expression." | 1.39 | Different cell cycle modulation by celecoxib at different concentrations. ( Kim, YM; Pyo, H, 2013) |
"Celecoxib combined with 5-FU could inhibit the growth of tumors in vivo by inducing apoptosis and activation of the cytochrome C dependency apoptosis signal pathway." | 1.39 | Increase of cyclooxygenase-2 inhibition with celecoxib combined with 5-FU enhances tumor cell apoptosis and antitumor efficacy in a subcutaneous implantation tumor model of human colon cancer. ( Chen, WC; Guo, Q; Zhang, DQ; Zhu, JH, 2013) |
"Human HT-29 colon cancer cells were exposed to carefully controlled hypoxic conditions and/or epidermal growth factor (EGF) and then investigated for EMT changes and signal transduction pathways involved by using morphological, molecular, and cell biology techniques." | 1.38 | Celecoxib inactivates epithelial-mesenchymal transition stimulated by hypoxia and/or epidermal growth factor in colon cancer cells. ( Bocca, C; Bozzo, F; Cannito, S; Miglietta, A; Parola, M, 2012) |
"HT-29 colon cancer cells and LT97 colorectal micro-adenoma cells derived from a patient with FAP, were exposed to low dose celecoxib and UDCA alone or in combination with tauro-cholic acid (CA) and tauro-chenodeoxycholic acid (CDCA), mimicking bile of FAP patients treated with UDCA." | 1.38 | Celecoxib and tauro-ursodeoxycholic acid co-treatment inhibits cell growth in familial adenomatous polyposis derived LT97 colon adenoma cells. ( Marian, B; Nagengast, FM; Peters, WH; Roelofs, HM; Te Morsche, RH; van Heumen, BW, 2012) |
"Combined treatment of human HCT116 colon cancer cells with free celecoxib plus tributyrin emulsion inhibited the cellular proliferation more effectively than that of each drug alone, suggesting the possibility of tributyrin emulsion as a potential celecoxib carrier." | 1.38 | Dual function of tributyrin emulsion: solubilization and enhancement of anticancer effect of celecoxib. ( Hong, SS; Kang, SN; Lee, MK; Lim, SJ, 2012) |
"Celecoxib has shown potential anticancer activity against most carcinomas, especially in patients with familial adenomatous polyposis and precancerous disease of the colon." | 1.37 | The potential of celecoxib-loaded hydroxyapatite-chitosan nanocomposite for the treatment of colon cancer. ( Azab, B; Dash, R; Fisher, PB; Kundu, SC; Mandal, M; Pathak, A; Prashanth Kumar, BN; Puvvada, N; Sarkar, D; Venkatesan, P, 2011) |
"Leukotriene B4 (LTB4) has been implicated in prostate and colon carcinogenesis, but little is known about the potential role of LTB4 in celecoxib-mediated anticancer effect." | 1.36 | Role of leukotriene B4 in celecoxib-mediated anticancer effect. ( Gao, P; Guan, L; Zheng, J, 2010) |
"Therefore, two clones of a human colon cancer cell line (HT-29) in which GPx2 was stably knocked down by small interfering RNA (siRNA; siGPx2) were used to test whether cancer-relevant processes are affected by GPx2." | 1.35 | Glutathione Peroxidase 2 Inhibits Cyclooxygenase-2-Mediated Migration and Invasion of HT-29 Adenocarcinoma Cells but Supports Their Growth as Tumors in Nude Mice. ( Banning, A; Brigelius-Flohé, R; Florian, S; Kipp, A; Krehl, S; Löwinger, M; Schmitmeier, S; Steinberg, P; Thalmann, S; Thierbach, R, 2008) |
"Progression of colon cancer is associated with the up-regulation of cyclooxygenase-2 (COX-2) and hydroxymethyl glutaryl CoA reductase (HMG-R)." | 1.35 | Synergistic effects of lovastatin and celecoxib on caveolin-1 and its down-stream signaling molecules: Implications for colon cancer prevention. ( Guruswamy, S; Rao, CV, 2009) |
"Celecoxib is a non-steroidal anti-inflammatory drug (NSAID) developed as a selective inhibitor of cyclooxygenase-2 (COX-2)." | 1.35 | Novel nitro-oxy derivatives of celecoxib for the regulation of colon cancer cell growth. ( Bassignana, A; Bocca, C; Boschi, D; Bozzo, F; Gasco, A; Lazzarato, L; Miglietta, A, 2009) |
"To evaluate the effects of celecoxib, in combination with oxaliplatin, on tumour growth, cell apoptosis and angiogenesis in nude mice models." | 1.35 | Synergistic inhibition effect of tumor growth by using celecoxib in combination with oxaliplatin. ( Bian, H; Cai, J; Gui, L; Zhao, F; Zhao, S, 2009) |
"Celecoxib treatment resulted in significantly altered expression levels of over 1,000 to 3,000 transcripts in these cell lines, respectively." | 1.35 | Altered gene expression profiles define pathways in colorectal cancer cell lines affected by celecoxib. ( Ajaz, S; Ali, IU; Fatima, N; Greenwald, P; Munroe, DJ; Stauffer, S; Stephens, RM; Yi, M, 2008) |
"Celecoxib was incubated for 4 h with HT29 cells and HUVEC and adhesion was quantified by a computerized micro-imaging system." | 1.35 | Celecoxib modulates adhesion of HT29 colon cancer cells to vascular endothelial cells by inhibiting ICAM-1 and VCAM-1 expression. ( Brucato, L; Collino, M; Dianzani, C; Fantozzi, R; Gallicchio, M; Rosa, AC, 2008) |
"Two human colon cancer cell lines (HCT-15 and HT-29) were treated with 5-FU and celecoxib, alone and in combination." | 1.34 | Celecoxib attenuates 5-fluorouracil-induced apoptosis in HCT-15 and HT-29 human colon cancer cells. ( Bae, YM; Chun, WJ; Lim, YJ; Rhee, JC, 2007) |
"The proliferation of colon cancer cells was determined by MTT assay, and the cell cycle progression was analyzed by flow cytometric assay." | 1.33 | [Effects of selective and non-selective cyclooxygenase-2 inhibitor on the growth of colon cancer cells]. ( Huang, MH; Li, X; Ouyang, Q; Tang, CW; Wang, CH, 2006) |
" Chronic use of high doses of these agents may induce side effects in ostensibly normal individuals." | 1.33 | Prevention of azoxymethane-induced colon cancer by combination of low doses of atorvastatin, aspirin, and celecoxib in F 344 rats. ( Khor, TO; Kong, AN; Kopelovich, L; Rao, CV; Reddy, BS; Steele, VE; Wang, CX; Zheng, X, 2006) |
" This study examined the dose-response effect of celecoxib when administered during the initiation and postinitiation stages." | 1.31 | Chemoprevention of colon cancer by specific cyclooxygenase-2 inhibitor, celecoxib, administered during different stages of carcinogenesis. ( Hirose, Y; Kelloff, G; Lubet, R; Paulson, S; Rao, CV; Reddy, BS; Seibert, K; Steele, V, 2000) |
" Groups 2 and 3 also received experimental diet containing celecoxib (500 and 1500 ppm, respectively) for 8 weeks, starting a week before the first dosing of AOM." | 1.31 | Suppression of occurrence and advancement of beta-catenin-accumulated crypts, possible premalignant lesions of colon cancer, by selective cyclooxygenase-2 inhibitor, celecoxib. ( Hara, A; Hirose, Y; Katayama, M; Kuno, T; Mori, H; Qiao, Z; Shimizu, M; Yamada, Y; Yoshimi, N, 2001) |
"Celecoxib was more potent than SC560." | 1.31 | COX-2 independent induction of cell cycle arrest and apoptosis in colon cancer cells by the selective COX-2 inhibitor celecoxib. ( Bräutigam, L; Geisslinger, G; Grösch, S; Niederberger, E; Tegeder, I, 2001) |
" Experiments were designed to assess the potential chemopreventive properties of highly selective iNOS inhibitors, administered individually and in combination with a selective COX-2 inhibitor, on the development of AOM-induced colonic aberrant crypt foci (ACF)." | 1.31 | Chemopreventive properties of a selective inducible nitric oxide synthase inhibitor in colon carcinogenesis, administered alone or in combination with celecoxib, a selective cyclooxygenase-2 inhibitor. ( Connor, JR; Indranie, C; Manning, PT; Rao, CV; Reddy, BS; Simi, B, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (3.36) | 18.2507 |
2000's | 58 (48.74) | 29.6817 |
2010's | 49 (41.18) | 24.3611 |
2020's | 8 (6.72) | 2.80 |
Authors | Studies |
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Ottanà, R | 1 |
Carotti, S | 1 |
Maccari, R | 1 |
Landini, I | 1 |
Chiricosta, G | 1 |
Caciagli, B | 1 |
Vigorita, MG | 1 |
Mini, E | 1 |
Ruiz, JF | 1 |
Kedziora, K | 1 |
Keogh, B | 1 |
Maguire, J | 1 |
Reilly, M | 1 |
Windle, H | 1 |
Kelleher, DP | 1 |
Gilmer, JF | 1 |
Bhardwaj, A | 2 |
Kaur, J | 2 |
Sharma, SK | 1 |
Huang, Z | 1 |
Wuest, F | 2 |
Knaus, EE | 2 |
Misra, S | 1 |
Ghatak, S | 1 |
Patil, N | 1 |
Dandawate, P | 1 |
Ambike, V | 1 |
Adsule, S | 1 |
Unni, D | 1 |
Venkateswara Swamy, K | 1 |
Padhye, S | 1 |
Maruyama, R | 1 |
Kiyohara, Y | 1 |
Kudo, Y | 1 |
Sugiyama, T | 1 |
Xu, H | 1 |
Li, P | 1 |
Ma, H | 1 |
Tan, Y | 1 |
Wang, X | 1 |
Cai, F | 1 |
Xu, J | 1 |
Sun, H | 1 |
Zhuang, H | 1 |
Hua, ZC | 1 |
Nicolini, A | 1 |
Ferrari, P | 1 |
Morganti, R | 1 |
Carpi, A | 1 |
Salim, EI | 2 |
Mahfouz, ME | 1 |
Kang, JS | 2 |
Hegazi, MM | 2 |
Helmy, HM | 2 |
Eltonouby, EA | 1 |
Lemmens, G | 1 |
Brouwers, J | 1 |
Snoeys, J | 1 |
Augustijns, P | 1 |
Vanuytsel, T | 1 |
Mao, L | 1 |
Yang, J | 1 |
Yue, J | 1 |
Chen, Y | 2 |
Zhou, H | 1 |
Fan, D | 1 |
Zhang, Q | 3 |
Buraschi, S | 1 |
Iozzo, RV | 1 |
Bi, X | 1 |
Srivastava, S | 1 |
Dewangan, J | 1 |
Mishra, S | 1 |
Divakar, A | 1 |
Chaturvedi, S | 1 |
Wahajuddin, M | 1 |
Kumar, S | 1 |
Rath, SK | 1 |
Yin, X | 1 |
Zhang, Y | 3 |
Wen, Y | 1 |
Yang, Y | 1 |
Chen, H | 1 |
Kerr, DJ | 1 |
Chamberlain, S | 1 |
Kerr, RS | 1 |
Meyerhardt, JA | 1 |
Shi, Q | 1 |
Fuchs, CS | 1 |
Meyer, J | 1 |
Niedzwiecki, D | 1 |
Zemla, T | 1 |
Kumthekar, P | 1 |
Guthrie, KA | 1 |
Couture, F | 1 |
Kuebler, P | 1 |
Bendell, JC | 1 |
Kumar, P | 1 |
Lewis, D | 1 |
Tan, B | 1 |
Bertagnolli, M | 1 |
Grothey, A | 1 |
Hochster, HS | 1 |
Goldberg, RM | 1 |
Venook, A | 1 |
Blanke, C | 1 |
O'Reilly, EM | 1 |
Shields, AF | 1 |
Jain, S | 2 |
Ghanghas, P | 2 |
Rana, C | 4 |
Sanyal, SN | 10 |
Buzharevski, A | 1 |
Paskas, S | 1 |
Sárosi, MB | 1 |
Laube, M | 1 |
Lönnecke, P | 1 |
Neumann, W | 1 |
Mijatovic, S | 1 |
Maksimovic-Ivanic, D | 1 |
Pietzsch, J | 1 |
Hey-Hawkins, E | 1 |
Piplani, H | 3 |
Vaish, V | 4 |
Vaiphei, K | 1 |
Setia, S | 3 |
Nehru, B | 4 |
Liu, Z | 1 |
Duan, ZJ | 1 |
Chang, JY | 1 |
Zhang, ZF | 1 |
Chu, R | 1 |
Li, YL | 1 |
Dai, KH | 1 |
Mo, GQ | 1 |
Chang, QY | 1 |
Edagawa, M | 1 |
Kawauchi, J | 1 |
Hirata, M | 2 |
Goshima, H | 1 |
Inoue, M | 1 |
Okamoto, T | 1 |
Murakami, A | 1 |
Maehara, Y | 1 |
Kitajima, S | 1 |
Kim, SJ | 1 |
Ha, GH | 1 |
Bae, JH | 1 |
Kim, GR | 1 |
Son, CH | 1 |
Park, YS | 1 |
Yang, K | 1 |
Oh, SO | 1 |
Kim, SH | 1 |
Kang, CD | 1 |
Fink, SP | 2 |
Dawson, DM | 1 |
Kresak, A | 1 |
Lawrence, EG | 1 |
Yang, P | 2 |
Barnholtz-Sloan, JS | 2 |
Willis, JE | 1 |
Kopelovich, L | 2 |
Markowitz, SD | 2 |
Venè, R | 1 |
Tosetti, F | 1 |
Minghelli, S | 1 |
Poggi, A | 1 |
Ferrari, N | 1 |
Benelli, R | 1 |
Tian, S | 1 |
Chang, W | 1 |
Du, H | 1 |
Bai, J | 1 |
Sun, Z | 1 |
Wang, H | 1 |
Zhu, G | 1 |
Tao, K | 1 |
Long, Y | 1 |
Zhang, L | 1 |
Tong, Y | 1 |
Zhang, X | 1 |
Pan, M | 1 |
Chen, S | 1 |
Pal, I | 1 |
Dey, KK | 1 |
Chaurasia, M | 1 |
Parida, S | 1 |
Das, S | 2 |
Rajesh, Y | 1 |
Sharma, K | 1 |
Chowdhury, T | 1 |
Mandal, M | 4 |
Bazan, L | 1 |
Bendas, ER | 1 |
El Gazayerly, ON | 1 |
Badawy, SS | 1 |
Li, W | 1 |
Liu, D | 2 |
Zhang, H | 1 |
Correia, A | 1 |
Mäkilä, E | 1 |
Salonen, J | 1 |
Hirvonen, J | 1 |
Santos, HA | 1 |
Schiffmann, S | 1 |
Maier, TJ | 3 |
Wobst, I | 1 |
Janssen, A | 2 |
Corban-Wilhelm, H | 1 |
Angioni, C | 1 |
Geisslinger, G | 4 |
Grösch, S | 4 |
Gradilone, A | 1 |
Pulcinelli, FM | 1 |
Lotti, LV | 1 |
Trifirò, E | 1 |
Martino, S | 1 |
Gandini, O | 1 |
Gianni, W | 1 |
Frati, L | 1 |
Aglianò, AM | 1 |
Gazzaniga, P | 1 |
Fatima, N | 2 |
Yi, M | 1 |
Ajaz, S | 1 |
Stephens, RM | 1 |
Stauffer, S | 2 |
Greenwald, P | 2 |
Munroe, DJ | 1 |
Ali, IU | 2 |
Takahashi-Yanaga, F | 2 |
Yoshihara, T | 1 |
Jingushi, K | 1 |
Miwa, Y | 2 |
Morimoto, S | 2 |
Sasaguri, T | 2 |
Banning, A | 1 |
Kipp, A | 1 |
Schmitmeier, S | 1 |
Löwinger, M | 1 |
Florian, S | 1 |
Krehl, S | 1 |
Thalmann, S | 1 |
Thierbach, R | 1 |
Steinberg, P | 1 |
Brigelius-Flohé, R | 1 |
Zhao, S | 1 |
Cai, J | 1 |
Bian, H | 1 |
Gui, L | 1 |
Zhao, F | 1 |
Foreman, JE | 1 |
Sorg, JM | 1 |
McGinnis, KS | 1 |
Rigas, B | 1 |
Williams, JL | 1 |
Clapper, ML | 2 |
Gonzalez, FJ | 1 |
Peters, JM | 1 |
Yan, M | 1 |
Myung, SJ | 1 |
Lawrence, E | 1 |
Lutterbaugh, J | 1 |
Zhou, X | 1 |
Rerko, RM | 1 |
Willis, J | 1 |
Dawson, D | 1 |
Tai, HH | 1 |
Newman, RA | 1 |
Bertagnolli, MM | 2 |
Yang, Z | 1 |
Xiao, H | 2 |
Jin, H | 1 |
Koo, PT | 1 |
Tsang, DJ | 1 |
Yang, CS | 2 |
Bozzo, F | 3 |
Bassignana, A | 2 |
Lazzarato, L | 1 |
Boschi, D | 1 |
Gasco, A | 1 |
Bocca, C | 3 |
Miglietta, A | 3 |
Winfield, LL | 1 |
Inniss, TR | 1 |
Smith, DM | 1 |
Guruswamy, S | 1 |
Rao, CV | 10 |
Venkatesan, P | 3 |
Krishnan, MM | 1 |
Chakraborty, C | 1 |
Chaudhury, K | 2 |
Kanwar, SS | 1 |
Roy, KR | 1 |
Reddanna, P | 1 |
Lynch, PM | 1 |
Ayers, GD | 1 |
Hawk, E | 1 |
Richmond, E | 1 |
Eagle, C | 1 |
Woloj, M | 1 |
Church, J | 1 |
Hasson, H | 1 |
Patterson, S | 1 |
Half, E | 1 |
Burke, CA | 1 |
Carothers, AM | 1 |
Davids, JS | 1 |
Damas, BC | 1 |
Liu, JP | 2 |
Wei, HB | 2 |
Zheng, ZH | 2 |
Guo, WP | 2 |
Fang, JF | 2 |
Gao, P | 1 |
Guan, L | 1 |
Zheng, J | 1 |
Puvvada, N | 1 |
Dash, R | 2 |
Prashanth Kumar, BN | 1 |
Sarkar, D | 2 |
Azab, B | 1 |
Pathak, A | 1 |
Kundu, SC | 1 |
Fisher, PB | 2 |
Sade, A | 1 |
Tunçay, S | 1 |
Cimen, I | 1 |
Severcan, F | 1 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Temozolomide and Irinotecan Consolidation in Patients With MGMT Silenced, Microsatellite Stable Colorectal Cancer With Persistence of Minimal Residual Disease in Liquid Biopsy After Standard Adjuvant Chemotherapy: the ERASE-TMZ Study[NCT05031975] | Phase 2 | 35 participants (Anticipated) | Interventional | 2022-05-02 | Recruiting | ||
A Phase III Trial of 6 Versus 12 Treatments of Adjuvant FOLFOX Plus Celecoxib or Placebo for Patients With Resected Stage III Colon Cancer[NCT01150045] | Phase 3 | 2,527 participants (Actual) | Interventional | 2010-06-30 | Active, not recruiting | ||
Phase I Pilot Toxicity/Methods Validation Study of Celecoxib in Genotype-Positive Children With Familial Adenomatous Polyposis[NCT00685568] | Phase 1 | 22 participants (Actual) | Interventional | 2002-11-21 | Completed | ||
Radiosensitization With a COX-2 Inhibitor (Celecoxib), With Chemoradiation for Cancer of the Head and Neck[NCT00581971] | Phase 1/Phase 2 | 30 participants (Actual) | Interventional | 2002-09-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Disease-Free Survival (DFS) is defined as the time of randomization until documented progression or death from any cause. The endpoint of this trial is to compare disease-free survival of patients with stage III colon cancer randomized to standard chemotherapy only (FOLFOX; Arm A and Arm C) or standard chemotherapy (FOLFOX) with 3 years of celecoxib 400 mg daily (Arm B and Arm D). The percentage of patients who were alive and disease free after 3 years are reported here. A log-rank test stratified with the stratification factors was used to compare disease-free survival (celecoxib vs placebo) (NCT01150045)
Timeframe: At 3 years of follow-up
Intervention | percentage of participants (Number) |
---|---|
FOLFOX and Placebo (Arms A +C) | 73.4 |
FOLFOX Plus Celecoxib Daily (Arms B + D) | 76.3 |
Overall Survival (DFS) is defined as the time of randomization until documented death from any cause. The endpoint is to compare overall survival of patients with stage III colon cancer randomized to standard chemotherapy only (FOLFOX; Arm A and Arm C) or standard chemotherapy (FOLFOX) with 5 years of celecoxib 400 mg daily (Arm B and Arm D). The percentage of patients who were alive after 3 years are reported here. (NCT01150045)
Timeframe: up to 3 years from registration
Intervention | percentage of participants (Number) |
---|---|
FOLFOX and Placebo (Arms A +C) | 81.6 |
FOLFOX Plus Celecoxib Daily (Arms B + D) | 84.3 |
Evaluate the response to concurrent celecoxib, carboplatin, paclitaxel, and radiotherapy in the treatment of locally advanced SSC of the head and neck. Response is determined by local control only, local and distant metastasis, distant metastasis only, second primary, and surgical salvage. (NCT00581971)
Timeframe: 2 years from end of treatment (Radiation therapy)
Intervention | Participants (Number) | ||||
---|---|---|---|---|---|
Local Control Only | Local Control and Distant Metastasis | Distant Metastatsis Only | Secondary Primary - Site Unknown | Surgical Salvage | |
Recurrence | 6 | 2 | 1 | 2 | 3 |
Particpants experiencing Acute Toxicities > Grade 3 (NCT00581971)
Timeframe: 2 years from radiation therapy
Intervention | participants (Number) | ||
---|---|---|---|
Hematologic | Dermatitis | Mucositis/Dysphagia | |
Acute Toxicity | 12 | 7 | 16 |
1 review available for celecoxib and Cancer of Colon
Article | Year |
---|---|
Chemoprophylaxis of colon cancer.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Celecoxib; Chemoprevention; | 2005 |
3 trials available for celecoxib and Cancer of Colon
Article | Year |
---|---|
Effect of Celecoxib vs Placebo Added to Standard Adjuvant Therapy on Disease-Free Survival Among Patients With Stage III Colon Cancer: The CALGB/SWOG 80702 (Alliance) Randomized Clinical Trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Celecoxib; Chemother | 2021 |
Effect of Celecoxib vs Placebo Added to Standard Adjuvant Therapy on Disease-Free Survival Among Patients With Stage III Colon Cancer: The CALGB/SWOG 80702 (Alliance) Randomized Clinical Trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Celecoxib; Chemother | 2021 |
Effect of Celecoxib vs Placebo Added to Standard Adjuvant Therapy on Disease-Free Survival Among Patients With Stage III Colon Cancer: The CALGB/SWOG 80702 (Alliance) Randomized Clinical Trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Celecoxib; Chemother | 2021 |
Effect of Celecoxib vs Placebo Added to Standard Adjuvant Therapy on Disease-Free Survival Among Patients With Stage III Colon Cancer: The CALGB/SWOG 80702 (Alliance) Randomized Clinical Trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Celecoxib; Chemother | 2021 |
15-Hydroxyprostaglandin dehydrogenase inactivation as a mechanism of resistance to celecoxib chemoprevention of colon tumors.
Topics: Adenoma; Animals; Celecoxib; Colon; Colonic Neoplasms; Colonoscopy; Drug and Narcotic Control; Human | 2009 |
The safety and efficacy of celecoxib in children with familial adenomatous polyposis.
Topics: Adenoma; Adenomatous Polyposis Coli; Adolescent; Celecoxib; Child; Cohort Studies; Colonic Neoplasms | 2010 |
115 other studies available for celecoxib and Cancer of Colon
Article | Year |
---|---|
In vitro antiproliferative activity against human colon cancer cell lines of representative 4-thiazolidinones. Part I.
Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Colonic Neoplasms; Cyclooxygenase 1; Cy | 2005 |
A double prodrug system for colon targeting of benzenesulfonamide COX-2 inhibitors.
Topics: Animals; Benzenesulfonamides; Caco-2 Cells; Celecoxib; Clostridium perfringens; Colon; Colonic Neopl | 2011 |
Hybrid fluorescent conjugates of COX-2 inhibitors: search for a COX-2 isozyme imaging cancer biomarker.
Topics: Acridines; Acridones; Biomarkers, Tumor; Celecoxib; Cell Line, Tumor; Colonic Neoplasms; Cyclooxygen | 2013 |
Novel dual cyclooxygenase and lipoxygenase inhibitors targeting hyaluronan-CD44v6 pathway and inducing cytotoxicity in colon cancer cells.
Topics: Antineoplastic Agents; Arachidonate 5-Lipoxygenase; Cell Line, Tumor; Cell Proliferation; Colonic Ne | 2013 |
Effects of the anti-inflammatory drug celecoxib on cell death signaling in human colon cancer.
Topics: Anti-Inflammatory Agents; Apoptosis; Celecoxib; Cell Death; Colonic Neoplasms; Cyclooxygenase 2 Inhi | 2023 |
ADT-OH synergistically enhanced the antitumor activity of celecoxib in human colorectal cancer cells.
Topics: Apoptosis; Celecoxib; Cell Line, Tumor; Cell Proliferation; Colonic Neoplasms; Humans; Thiones | 2023 |
Treatment of Metastatic or High-Risk Solid Cancer Patients by Targeting the Immune System and/or Tumor Burden: Six Cases Reports.
Topics: Adult; Aged; alpha-Tocopherol; Antineoplastic Agents; Breast Neoplasms; Celecoxib; Colonic Neoplasms | 2019 |
Celecoxib Targeted Therapy Attenuates Mouse Colon Carcinogenesis through Modulation of Expression Patterns of Cancer Stem Cells.
Topics: 1,2-Dimethylhydrazine; Animals; Carcinogenesis; Carcinogens; Celecoxib; Colonic Neoplasms; Cyclooxyg | 2019 |
Insight into the Colonic Disposition of Sulindac in Humans.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Colonic Neoplasms; Colorectal Neoplasms; Humans; | 2021 |
Decorin deficiency promotes epithelial-mesenchymal transition and colon cancer metastasis.
Topics: Animals; Azoxymethane; beta Catenin; Cadherins; Cancer-Associated Fibroblasts; Celecoxib; Colitis-As | 2021 |
Piperine and Celecoxib synergistically inhibit colon cancer cell proliferation via modulating Wnt/β-catenin signaling pathway.
Topics: Alkaloids; Animals; Antineoplastic Agents; Apoptosis; Benzodioxoles; beta Catenin; Celecoxib; Cell L | 2021 |
Celecoxib alleviates zinc deficiency-promoted colon tumorigenesis through suppressing inflammation.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Carcinogenesis; Celecoxib; Colonic Neoplasms; Infl | 2021 |
Celecoxib for Stage III Colon Cancer.
Topics: Celecoxib; Colonic Neoplasms; Disease-Free Survival; Humans; Reference Standards; Sulfonamides | 2021 |
Role of GSK-3β in Regulation of Canonical Wnt/β-catenin Signaling and PI3-K/Akt Oncogenic Pathway in Colon Cancer.
Topics: 1,2-Dimethylhydrazine; Animals; Anticarcinogenic Agents; Apoptosis; Celecoxib; Cell Transformation, | 2017 |
Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines.
Topics: Animals; Antineoplastic Agents; Celecoxib; Cell Death; Cell Line, Tumor; Cell Proliferation; Cell Su | 2019 |
Dolastatin, along with Celecoxib, stimulates apoptosis by a mechanism involving oxidative stress, membrane potential change and PI3-K/AKT pathway down regulation.
Topics: Adenosine Triphosphate; Animals; Apoptosis; Binding Sites; Celecoxib; Cell Cycle Proteins; Colonic N | 2013 |
Activation of NF-κB: bridging the gap between inflammation and cancer in colitis-mediated colon carcinogenesis.
Topics: 1,2-Dimethylhydrazine; Animals; Celecoxib; Colitis, Ulcerative; Colonic Neoplasms; Cyclooxygenase 2 | 2014 |
Fluorophore-labeled cyclooxygenase-2 inhibitors for the imaging of cyclooxygenase-2 overexpression in cancer: synthesis and biological studies.
Topics: 4-Chloro-7-nitrobenzofurazan; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Cell Line, Tumor; | 2014 |
Sinomenine sensitizes multidrug-resistant colon cancer cells (Caco-2) to doxorubicin by downregulation of MDR-1 expression.
Topics: Antibiotics, Antineoplastic; ATP Binding Cassette Transporter, Subfamily B, Member 1; Caco-2 Cells; | 2014 |
Role of activating transcription factor 3 (ATF3) in endoplasmic reticulum (ER) stress-induced sensitization of p53-deficient human colon cancer cells to tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL)-mediated apoptosis through up-re
Topics: Activating Transcription Factor 3; Apoptosis; Base Sequence; Celecoxib; Cell Line, Tumor; Colonic Ne | 2014 |
The PI3K/Akt pathway in colitis associated colon cancer and its chemoprevention with celecoxib, a Cox-2 selective inhibitor.
Topics: Animals; Celecoxib; Chemoprevention; Colitis; Colonic Neoplasms; Cyclooxygenase 2 Inhibitors; Mice; | 2014 |
COX-2- and endoplasmic reticulum stress-independent induction of ULBP-1 and enhancement of sensitivity to NK cell-mediated cytotoxicity by celecoxib in colon cancer cells.
Topics: AC133 Antigen; Antigens, CD; Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenase 2 Inhibi | 2015 |
Celecoxib prevents colitis associated colon carcinogenesis: an upregulation of apoptosis.
Topics: Apoptosis; Celecoxib; Cell Cycle Checkpoints; Cell Proliferation; Colitis, Ulcerative; Colon; Coloni | 2014 |
Sulindac reversal of 15-PGDH-mediated resistance to colon tumor chemoprevention with NSAIDs.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Aspirin; Azoxymethane; Carc | 2015 |
Celecoxib increases EGF signaling in colon tumor associated fibroblasts, modulating EGFR expression and degradation.
Topics: Blotting, Western; Celecoxib; Cell Line, Tumor; Cell Proliferation; Colonic Neoplasms; Cyclooxygenas | 2015 |
The interplay between GRP78 expression and Akt activation in human colon cancer cells under celecoxib treatment.
Topics: Antineoplastic Agents; Apoptosis; Celecoxib; Cell Line, Tumor; Chromones; Colonic Neoplasms; Endopla | 2015 |
Arsenic sulfide combined with JQ1, chemotherapy agents, or celecoxib inhibit gastric and colon cancer cell growth.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Arsenicals; Azepines; Camptothecin; Celec | 2015 |
Cooperative effect of BI-69A11 and celecoxib enhances radiosensitization by modulating DNA damage repair in colon carcinoma.
Topics: Apoptosis; Benzimidazoles; Carcinoma; Celecoxib; Colonic Neoplasms; Combined Modality Therapy; DNA B | 2016 |
Expression Patterns of Cancer Stem Cell Markers During Specific Celecoxib Therapy in Multistep Rat Colon Carcinogenesis Bioassays.
Topics: Aldehyde Dehydrogenase 1 Family; Animals; Biological Assay; Biomarkers, Tumor; Carcinogenesis; Celec | 2016 |
Comparative pharmaceutical study on colon targeted micro-particles of celecoxib: in-vitro-in-vivo evaluation.
Topics: Acetic Acid; Acrylic Resins; Animals; Celecoxib; Chemistry, Pharmaceutical; Colon; Colonic Neoplasms | 2016 |
Microfluidic assembly of a nano-in-micro dual drug delivery platform composed of halloysite nanotubes and a pH-responsive polymer for colon cancer therapy.
Topics: Aluminum Silicates; Atorvastatin; Caco-2 Cells; Celecoxib; Cell Death; Cell Proliferation; Cell Surv | 2017 |
Chemoprevention of Colon Cancer through Inhibition of Angiogenesis and Induction of Apoptosis by Nonsteroidal Anti-Inflammatory Drugs.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Anticarcinogenic Agents; Apoptosis; Celecoxib; Col | 2016 |
The anti-proliferative potency of celecoxib is not a class effect of coxibs.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Apoptosis; beta Catenin; Celecoxib; Cell Cycle; Ce | 2008 |
Celecoxib upregulates multidrug resistance proteins in colon cancer: lack of synergy with standard chemotherapy.
Topics: ATP Binding Cassette Transporter, Subfamily B; Blotting, Western; Celecoxib; Cell Membrane; Cell Sur | 2008 |
Altered gene expression profiles define pathways in colorectal cancer cell lines affected by celecoxib.
Topics: Blotting, Western; Celecoxib; Cell Line, Tumor; Colonic Neoplasms; Cyclooxygenase 2 Inhibitors; Gene | 2008 |
Celecoxib-induced degradation of T-cell factors-1 and -4 in human colon cancer cells.
Topics: Anti-Inflammatory Agents, Non-Steroidal; beta Catenin; Celecoxib; Cell Line, Tumor; Colonic Neoplasm | 2008 |
Glutathione Peroxidase 2 Inhibits Cyclooxygenase-2-Mediated Migration and Invasion of HT-29 Adenocarcinoma Cells but Supports Their Growth as Tumors in Nude Mice.
Topics: Adenocarcinoma; Animals; Celecoxib; Cell Growth Processes; Cell Movement; Colonic Neoplasms; Cycloox | 2008 |
Synergistic inhibition effect of tumor growth by using celecoxib in combination with oxaliplatin.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; beta Catenin; Celecoxib; Cell Pr | 2009 |
Regulation of peroxisome proliferator-activated receptor-beta/delta by the APC/beta-CATENIN pathway and nonsteroidal antiinflammatory drugs.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; beta Catenin; Blotting, Western; Celecoxib; Coloni | 2009 |
Synergistic actions of atorvastatin with gamma-tocotrienol and celecoxib against human colon cancer HT29 and HCT116 cells.
Topics: Atorvastatin; Celecoxib; Cell Cycle; Cell Division; Cell Line, Tumor; Chromans; Colonic Neoplasms; C | 2010 |
Novel nitro-oxy derivatives of celecoxib for the regulation of colon cancer cell growth.
Topics: beta Catenin; Cadherins; Celecoxib; Cell Line, Tumor; Cell Proliferation; Cell Survival; Colonic Neo | 2009 |
Structure activity relationship of antiproliferative agents using multiple linear regression.
Topics: Algorithms; Antineoplastic Agents; Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenase 2 | 2009 |
Synergistic effects of lovastatin and celecoxib on caveolin-1 and its down-stream signaling molecules: Implications for colon cancer prevention.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Blotting, Western; Caveolin 1; Celecoxib; | 2009 |
Effect of AEE788 and/or Celecoxib on colon cancer cell morphology using advanced microscopic techniques.
Topics: Antineoplastic Agents; Celecoxib; Cell Shape; Colonic Neoplasms; Cytoskeleton; Epithelial Cells; Hum | 2010 |
Na(+)-stimulated Na+/H+ exchange and an unfavorable Ca2+ homeostasis initiate the cycloxygenase-2 inhibitors-induced apoptotic signals in colonic epithelial cells during the early stage of colon carcinogenesis.
Topics: 1,2-Dimethylhydrazine; Animals; Apoptosis; Calcium; Caspases; Celecoxib; Colon; Colonic Neoplasms; C | 2009 |
Persistent cyclooxygenase-2 inhibition downregulates NF-{kappa}B, resulting in chronic intestinal inflammation in the min/+ mouse model of colon tumorigenesis.
Topics: Animals; Antigens, CD34; Celecoxib; Cell Transformation, Neoplastic; Colitis; Colonic Neoplasms; Cyc | 2010 |
Celecoxib increases retinoid sensitivity in human colon cancer cell lines.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Celecoxib; Cell Line, Tumor; Colonic Neop | 2010 |
Antiproliferative effect of a novel nitro-oxy derivative of celecoxib in human colon cancer cells: role of COX-2 and nitric oxide.
Topics: Apoptosis; Benzyl Compounds; beta Catenin; Celecoxib; Cell Growth Processes; Cell Membrane; Cell Nuc | 2010 |
Role of leukotriene B4 in celecoxib-mediated anticancer effect.
Topics: Antineoplastic Agents; Celecoxib; Cell Line, Tumor; Cell Proliferation; Cell Survival; Colonic Neopl | 2010 |
[Celecoxib increased cellular ATRA sensitivity of human colon cancer cell lines through COX-2-independent mechanisms].
Topics: Antineoplastic Agents; Apoptosis; Celecoxib; Cell Line, Tumor; Cell Survival; Colonic Neoplasms; Cyc | 2009 |
The potential of celecoxib-loaded hydroxyapatite-chitosan nanocomposite for the treatment of colon cancer.
Topics: Animals; Antineoplastic Agents; Celecoxib; Cell Cycle; Cell Proliferation; Chitosan; Colonic Neoplas | 2011 |
Celecoxib reduces fluidity and decreases metastatic potential of colon cancer cell lines irrespective of COX-2 expression.
Topics: Antineoplastic Agents; Celecoxib; Cell Membrane; Cell Movement; Cell Proliferation; Colonic Neoplasm | 2012 |
Chemoprevention: First line of defence.
Topics: Animals; Aspirin; Celecoxib; Clinical Trials, Phase II as Topic; Colonic Neoplasms; Cyclooxygenase I | 2011 |
Cooperative enhancement of radiosensitivity after combined treatment of 17-(allylamino)-17-demethoxygeldanamycin and celecoxib in human lung and colon cancer cell lines.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Ataxia Telangiectasia Mutated Proteins; Ben | 2012 |
Celecoxib inactivates epithelial-mesenchymal transition stimulated by hypoxia and/or epidermal growth factor in colon cancer cells.
Topics: beta Catenin; Cadherins; Celecoxib; Cell Hypoxia; Cell Proliferation; Colonic Neoplasms; Cyclooxygen | 2012 |
Chronic anti-inflammatory drug therapy inhibits gel-forming mucin production in a murine xenograft model of human pseudomyxoma peritonei.
Topics: Administration, Oral; Animals; Anti-Inflammatory Agents; Appendiceal Neoplasms; Celecoxib; Colonic N | 2012 |
Chemopreventive efficacy of Targretin in rodent models of urinary bladder, colon/intestine, head and neck and mammary cancers.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Anticarcinogenic Agents; Bexarotene; Celecoxib; Co | 2012 |
Celecoxib and tauro-ursodeoxycholic acid co-treatment inhibits cell growth in familial adenomatous polyposis derived LT97 colon adenoma cells.
Topics: Adenoma; Adenomatous Polyposis Coli; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Cele | 2012 |
Role of Sulindac and Celecoxib in the regulation of angiogenesis during the early neoplasm of colon: exploring PI3-K/PTEN/Akt pathway to the canonical Wnt/β-catenin signaling.
Topics: Angiogenesis Inhibitors; Animals; Anti-Inflammatory Agents, Non-Steroidal; Apoptosis; Blotting, West | 2012 |
Dual function of tributyrin emulsion: solubilization and enhancement of anticancer effect of celecoxib.
Topics: Animals; Antineoplastic Agents; Celecoxib; Cell Line, Tumor; Cell Proliferation; Colonic Neoplasms; | 2012 |
Dolastatin 15, a mollusk linear peptide, and Celecoxib, a selective cyclooxygenase-2 inhibitor, prevent preneoplastic colonic lesions and induce apoptosis through inhibition of the regulatory transcription factor NF-κB and an inflammatory protein, iNOS.
Topics: Animals; Apoptosis; Blotting, Western; Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenas | 2012 |
Up-regulation of p53 and mitochondrial signaling pathway in apoptosis by a combination of COX-2 inhibitor, Celecoxib and Dolastatin 15, a marine mollusk linear peptide in experimental colon carcinogenesis.
Topics: Animals; Anticarcinogenic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Carcino | 2013 |
Inhibition of COX-2 in colon cancer modulates tumor growth and MDR-1 expression to enhance tumor regression in therapy-refractory cancers in vivo.
Topics: Adult; Aged; Animals; Antineoplastic Agents; Apoptosis; Aspirin; ATP Binding Cassette Transporter, S | 2012 |
AEE788 potentiates celecoxib-induced growth inhibition and apoptosis in human colon cancer cells.
Topics: Actins; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; C | 2012 |
Celecoxib downregulates CD133 expression through inhibition of the Wnt signaling pathway in colon cancer cells.
Topics: AC133 Antigen; Antigens, CD; Celecoxib; Cell Differentiation; Cell Line, Tumor; Cell Proliferation; | 2013 |
Different cell cycle modulation by celecoxib at different concentrations.
Topics: Adenocarcinoma; Apoptosis; Celecoxib; Cell Cycle; Cell Proliferation; Colonic Neoplasms; Cyclooxygen | 2013 |
Increase of cyclooxygenase-2 inhibition with celecoxib combined with 5-FU enhances tumor cell apoptosis and antitumor efficacy in a subcutaneous implantation tumor model of human colon cancer.
Topics: Animals; Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; | 2013 |
Expression of LGR-5, MSI-1 and DCAMKL-1, putative stem cell markers, in the early phases of 1,2-dimethylhydrazine-induced rat colon carcinogenesis: correlation with nuclear β-catenin.
Topics: 1,2-Dimethylhydrazine; Adenoma; Animals; beta Catenin; Biomarkers, Tumor; Celecoxib; Cell Nucleus; C | 2013 |
New combination promising against colon cancer.
Topics: Animals; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemothe | 2001 |
Inhibition of COX-2 in colon cancer cell lines by celecoxib increases the nuclear localization of active p53.
Topics: Antineoplastic Agents; Celecoxib; Cell Division; Cell Nucleus; Colonic Neoplasms; Cyclin-Dependent K | 2003 |
Inhibition of angiotensin II activity enhanced the antitumor effect of cyclooxygenase-2 inhibitors via insulin-like growth factor I receptor pathway.
Topics: Angiotensin II; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Animals; | 2003 |
Synergy between celecoxib and radiotherapy results from inhibition of cyclooxygenase-2-derived prostaglandin E2, a survival factor for tumor and associated vasculature.
Topics: Animals; Antineoplastic Agents; Carcinoma; Celecoxib; Colonic Neoplasms; Combined Modality Therapy; | 2004 |
Modulation of cyclooxygenase-2 activities by the combined action of celecoxib and decosahexaenoic acid: novel strategies for colon cancer prevention and treatment.
Topics: Apoptosis; Celecoxib; Cell Division; Cell Line, Tumor; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxy | 2004 |
Cyclooxygenase-2 (COX-2)-dependent and -independent anticarcinogenic effects of celecoxib in human colon carcinoma cells.
Topics: Anticarcinogenic Agents; Apoptosis; Caco-2 Cells; Celecoxib; Cell Cycle; Cell Cycle Proteins; Cell S | 2004 |
Correspondence re: M. V. Swamy et al., Inhibition of COX-2 in colon cancer cell lines by celecoxib increases the nuclear localization of active p53. Cancer Res 2003;63:5239-42.
Topics: Antineoplastic Agents; Celecoxib; Cell Line, Tumor; Cell Nucleus; Colonic Neoplasms; Cyclooxygenase | 2004 |
Modulation by celecoxib and difluoromethylornithine of the methylation of DNA and the estrogen receptor-alpha gene in rat colon tumors.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Azoxymethane; Biomarkers, Tumor; Carcinogen | 2004 |
COX-2 inhibitors still eyed for cancer prevention.
Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Breast Neoplasms; Celecoxib; Colonic Neoplasms; Cycl | 2005 |
Targeting the beta-catenin/APC pathway: a novel mechanism to explain the cyclooxygenase-2-independent anticarcinogenic effects of celecoxib in human colon carcinoma cells.
Topics: Adenomatous Polyposis Coli Protein; Anti-Inflammatory Agents, Non-Steroidal; Anticarcinogenic Agents | 2005 |
Spectral markers in preneoplastic intestinal mucosa: an accurate predictor of tumor risk in the MIN mouse.
Topics: Animals; Celecoxib; Colonic Neoplasms; Cyclooxygenase Inhibitors; Intestinal Mucosa; Male; Mice; Mic | 2005 |
Effect of concomitant polyethylene glycol and celecoxib on colonic aberrant crypt foci and tumors in F344 rats.
Topics: Animals; Azoxymethane; Bromodeoxyuridine; Celecoxib; Colon; Colonic Neoplasms; Cyclooxygenase Inhibi | 2005 |
Prevention of colon cancer by low doses of celecoxib, a cyclooxygenase inhibitor, administered in diet rich in omega-3 polyunsaturated fatty acids.
Topics: Animals; Azoxymethane; Carcinogens; Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenase 2 | 2005 |
Glycine-extended gastrin stimulates proliferation and inhibits apoptosis in colon cancer cells via cyclo-oxygenase-independent pathways.
Topics: Apoptosis; Celecoxib; Cell Count; Cell Proliferation; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxyg | 2006 |
Celecoxib induces anoikis in human colon carcinoma cells associated with the deregulation of focal adhesions and nuclear translocation of p130Cas.
Topics: Anoikis; Carcinoma; Celecoxib; Cell Nucleus; Colonic Neoplasms; Crk-Associated Substrate Protein; Cy | 2006 |
Glycine-extended gastrin inhibits apoptosis in colon cancer cells via separate activation of Akt and JNK pathways.
Topics: Anthracenes; Apoptosis; Celecoxib; Cell Line, Tumor; Cell Survival; Chromones; Colonic Neoplasms; Ga | 2006 |
Prevention of azoxymethane-induced colon cancer by combination of low doses of atorvastatin, aspirin, and celecoxib in F 344 rats.
Topics: Animals; Anticarcinogenic Agents; Apoptosis; Aspirin; Atorvastatin; Azoxymethane; Carcinogens; Celec | 2006 |
[Effects of selective and non-selective cyclooxygenase-2 inhibitor on the growth of colon cancer cells].
Topics: Apoptosis; Aspirin; Celecoxib; Cell Line, Tumor; Cell Proliferation; Colonic Neoplasms; Cyclooxygena | 2006 |
Proteomic profiling identifies cyclooxygenase-2-independent global proteomic changes by celecoxib in colorectal cancer cells.
Topics: Blotting, Western; Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cycl | 2006 |
Risk and risk reduction involving arginine intake and meat consumption in colorectal tumorigenesis and survival.
Topics: Acetyltransferases; Adult; Aged; Aged, 80 and over; Animals; Anti-Inflammatory Agents, Non-Steroidal | 2007 |
Inhibition of 5-lipoxygenase by MK886 augments the antitumor activity of celecoxib in human colon cancer cells.
Topics: Aged; Animals; Antineoplastic Agents; Arachidonate 5-Lipoxygenase; bcl-2-Associated X Protein; Caco- | 2006 |
Celecoxib inhibits the expression of survivin via the suppression of promoter activity in human colon cancer cells.
Topics: Anti-Inflammatory Agents, Non-Steroidal; beta Catenin; Celecoxib; Colonic Neoplasms; Cyclin D1; Gene | 2007 |
Down-regulation of PGE2 by physiologic levels of celecoxib is not sufficient to induce apoptosis or inhibit cell proliferation in human colon carcinoma cell lines.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Apoptosis; Carcinoma; Celecoxib; Cel | 2007 |
A target-selected Apc-mutant rat kindred enhances the modeling of familial human colon cancer.
Topics: Adenomatous Polyposis Coli Protein; Animals; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Col | 2007 |
Synergistic antitumor effects of celecoxib with 5-fluorouracil depend on IFN-gamma.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Celecoxib; Colonic Neoplasms; Cyclooxygenas | 2007 |
Celecoxib attenuates 5-fluorouracil-induced apoptosis in HCT-15 and HT-29 human colon cancer cells.
Topics: Adenocarcinoma; Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Apo | 2007 |
Interaction between celecoxib and docetaxel or cisplatin in human cell lines of ovarian cancer and colon cancer is independent of COX-2 expression levels.
Topics: Antineoplastic Agents; Apoptosis; Celecoxib; Cell Division; Cell Line, Tumor; Cisplatin; Colonic Neo | 2008 |
Celecoxib modulates adhesion of HT29 colon cancer cells to vascular endothelial cells by inhibiting ICAM-1 and VCAM-1 expression.
Topics: Blotting, Western; Celecoxib; Cell Adhesion; Cells, Cultured; Colonic Neoplasms; Cyclooxygenase Inhi | 2008 |
Celecoxib decreases expression of the adhesion molecules ICAM-1 and VCAM-1 in a colon cancer cell line (HT29).
Topics: Apoptosis; Celecoxib; Cell Adhesion; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenase Inhibitors; | 2008 |
Celecoxib-induced growth inhibition in SW480 colon cancer cells is associated with activation of protein kinase G.
Topics: Apoptosis; Celecoxib; Cell Adhesion Molecules; Cell Proliferation; Colonic Neoplasms; Cyclic GMP; Cy | 2008 |
Combination of atorvastatin and celecoxib synergistically induces cell cycle arrest and apoptosis in colon cancer cells.
Topics: Apoptosis; Atorvastatin; Celecoxib; Cell Cycle; Cell Survival; Colonic Neoplasms; Cyclooxygenase Inh | 2008 |
Cyclooxygenase-2 inhibition inhibits c-Met kinase activity and Wnt activity in colon cancer.
Topics: Aspirin; Celecoxib; Cell Line, Tumor; Colonic Neoplasms; Cyclooxygenase 2 Inhibitors; Glycogen Synth | 2008 |
Celecoxib inhibits tumor growth and angiogenesis in an orthotopic implantation tumor model of human colon cancer.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Apoptosis; Celecoxib; Cell Proliferation; Colonic Ne | 2008 |
Drugs to prevent colon cancer show promise, but hurdles remain for chemoprevention.
Topics: Adenoma; Animals; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Combined Chemotherapy Prot | 2008 |
Chemopreventive activity of celecoxib, a specific cyclooxygenase-2 inhibitor, against colon carcinogenesis.
Topics: Animals; Anticarcinogenic Agents; Azoxymethane; Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cycl | 1998 |
[APHS and celecoxib, the new aspirins have arrived].
Topics: Celecoxib; Colonic Neoplasms; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibito | 1998 |
Early trials probe COX-2 inhibitors' cancer-fighting potential.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Clinical Trials as Topic; Colonic Neoplasms; Cyc | 1999 |
Colon cancer prevention. Worth the trouble.
Topics: Adult; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Celecoxib; Colonic Neoplasms; Diet; Female; | 1999 |
Chemoprevention of colon cancer by specific cyclooxygenase-2 inhibitor, celecoxib, administered during different stages of carcinogenesis.
Topics: Administration, Oral; Animals; Anticarcinogenic Agents; Azoxymethane; Celecoxib; Colonic Neoplasms; | 2000 |
Proapoptotic anti-inflammatory drugs.
Topics: Angiogenesis Inhibitors; Animals; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Ce | 2001 |
Suppression of occurrence and advancement of beta-catenin-accumulated crypts, possible premalignant lesions of colon cancer, by selective cyclooxygenase-2 inhibitor, celecoxib.
Topics: Animals; Anticarcinogenic Agents; Azoxymethane; beta Catenin; Celecoxib; Cell Division; Cell Nucleus | 2001 |
COX-2 independent induction of cell cycle arrest and apoptosis in colon cancer cells by the selective COX-2 inhibitor celecoxib.
Topics: Animals; Apoptosis; Blotting, Western; Caco-2 Cells; Celecoxib; Cell Cycle; Cell Cycle Proteins; Cel | 2001 |
Chemopreventive properties of a selective inducible nitric oxide synthase inhibitor in colon carcinogenesis, administered alone or in combination with celecoxib, a selective cyclooxygenase-2 inhibitor.
Topics: Animals; Anticarcinogenic Agents; Azoxymethane; Body Weight; Carcinogens; Celecoxib; Colon; Colonic | 2002 |
Cyclooxygenase-2 inhibition by celecoxib reduces proliferation and induces apoptosis in angiogenic endothelial cells in vivo.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Apoptosis; Celecoxib; Cell Division; Coloni | 2002 |
Lamin B, caspase-3 activity, and apoptosis induction by a combination of HMG-CoA reductase inhibitor and COX-2 inhibitors: a novel approach in developing effective chemopreventive regimens.
Topics: Apoptosis; Caspase 3; Caspases; Celecoxib; Cell Survival; Colonic Neoplasms; Cyclooxygenase Inhibito | 2002 |
Celecoxib induces apoptosis by inhibiting 3-phosphoinositide-dependent protein kinase-1 activity in the human colon cancer HT-29 cell line.
Topics: 3-Phosphoinositide-Dependent Protein Kinases; Apoptosis; Celecoxib; Cell Survival; Colonic Neoplasms | 2002 |
COX-2 and prostanoid receptors: good targets for chemoprevention.
Topics: Animals; Breast Neoplasms; Celecoxib; Cell Transformation, Neoplastic; Chemoprevention; Colonic Neop | 2002 |