Page last updated: 2024-10-24

celecoxib and Experimental Neoplasms

celecoxib has been researched along with Experimental Neoplasms in 15 studies

Research Excerpts

ExcerptRelevanceReference
"Colorectal cancer has been found to be attenuated either with prophylactic manipulation of gut microbiome with probiotics or celecoxib, a non-steroidal anti-inflammatory drug mainly by suppressing early pro-carcinogenic markers in various experimental studies."7.88Prophylactic intervention of probiotics (L.acidophilus, L.rhamnosus GG) and celecoxib modulate Bax-mediated apoptosis in 1,2-dimethylhydrazine-induced experimental colon carcinogenesis. ( Chandel, D; Sharaf, LK; Sharma, M; Shukla, G, 2018)
"Alpha-TEA, a nonhydrolyzable ether analog of vitamin E (RRR-alpha-tocopherol), and celecoxib, a specific COX-2 inhibitor, were delivered separately or in combination to investigate their anticancer properties, using MDA-MB-435-FL-GFP human breast cancer xenografts in nude mice."7.72Vitamin E analog alpha-TEA and celecoxib alone and together reduce human MDA-MB-435-FL-GFP breast cancer burden and metastasis in nude mice. ( Kline, K; Lawson, KA; Sanders, BG; Simmons-Menchaca, M; Sun, L; Zhang, S, 2004)
"Colorectal cancer has been found to be attenuated either with prophylactic manipulation of gut microbiome with probiotics or celecoxib, a non-steroidal anti-inflammatory drug mainly by suppressing early pro-carcinogenic markers in various experimental studies."3.88Prophylactic intervention of probiotics (L.acidophilus, L.rhamnosus GG) and celecoxib modulate Bax-mediated apoptosis in 1,2-dimethylhydrazine-induced experimental colon carcinogenesis. ( Chandel, D; Sharaf, LK; Sharma, M; Shukla, G, 2018)
"Alpha-TEA, a nonhydrolyzable ether analog of vitamin E (RRR-alpha-tocopherol), and celecoxib, a specific COX-2 inhibitor, were delivered separately or in combination to investigate their anticancer properties, using MDA-MB-435-FL-GFP human breast cancer xenografts in nude mice."3.72Vitamin E analog alpha-TEA and celecoxib alone and together reduce human MDA-MB-435-FL-GFP breast cancer burden and metastasis in nude mice. ( Kline, K; Lawson, KA; Sanders, BG; Simmons-Menchaca, M; Sun, L; Zhang, S, 2004)
"Celecoxib was administered as 400 mg, twice daily starting on day 2 of cycle 1."2.73Celecoxib and mucosal protection: translation from an animal model to a phase I clinical trial of celecoxib, irinotecan, and 5-fluorouracil. ( Cao, S; Creaven, PJ; Durrani, FA; Iyer, RV; Javle, MM; Lawrence, DD; Noel, DC; Pendyala, L; Rustum, YM; Smith, PF, 2007)
"Celecoxib is an effective inhibitor of COX-2, used in anti-inflammation."1.48Celecoxib Conjugated Fluorescent Probe for Identification and Discrimination of Cyclooxygenase-2 Enzyme in Cancer Cells. ( Cui, H; Du, J; Fan, J; Gurram, B; Li, H; Li, M; Peng, X; Wang, J; Xie, Y; Zhang, S, 2018)
"Celecoxib has also a possible involvement with redox homeostasis, because its administration caused significant changes in the activity of oxidative enzymes, such as catalase and superoxide dismutase."1.36Celecoxib prevents tumor growth in an animal model by a COX-2 independent mechanism. ( Acco, A; Ávila, TV; Bastos-Pereira, AL; Cadena, SM; Cristina da Silva de Assis, H; Donatti, L; Lugarini, D; Muscará, MN; Oliveira-Christoff, Ad; Pires, Ado R; Teixeira, S, 2010)

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (40.00)29.6817
2010's9 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gurram, B1
Zhang, S2
Li, M1
Li, H1
Xie, Y1
Cui, H1
Du, J1
Fan, J1
Wang, J2
Peng, X1
Sharaf, LK1
Sharma, M1
Chandel, D1
Shukla, G1
Ding, N1
Cui, XX1
Gao, Z1
Huang, H1
Wei, X1
Du, Z1
Lin, Y1
Shih, WJ1
Rabson, AB1
Conney, AH1
Hu, C1
Zheng, X1
Xiang, HG1
Xie, X1
Hu, FQ1
Xiao, HB1
Zhang, WJ1
Chen, L1
Balansky, R1
Ganchev, G1
Iltcheva, M1
Nikolov, M1
La Maestra, S1
Micale, RT1
D'Agostini, F1
Steele, VE1
De Flora, S1
Ilhan, N1
Gungor, H1
Gul, HF1
Eroksuz, H1
Colby, JK1
Klein, RD1
McArthur, MJ1
Conti, CJ1
Kiguchi, K1
Kawamoto, T1
Riggs, PK1
Pavone, AI1
Sawicki, J1
Fischer, SM1
Maussang, D1
Langemeijer, E1
Fitzsimons, CP1
Stigter-van Walsum, M1
Dijkman, R1
Borg, MK1
Slinger, E1
Schreiber, A1
Michel, D1
Tensen, CP1
van Dongen, GA1
Leurs, R1
Smit, MJ1
Bastos-Pereira, AL1
Lugarini, D1
Oliveira-Christoff, Ad1
Ávila, TV1
Teixeira, S1
Pires, Ado R1
Muscará, MN1
Cadena, SM1
Donatti, L1
Cristina da Silva de Assis, H1
Acco, A1
Li, W1
Jiang, HR1
Xu, XL1
Zhang, J1
Liu, ML1
Zhai, LY1
Yu, L1
Chen, M1
Li, Z1
Wen, J1
Fu, J1
Guo, D1
Jiang, Y1
Wu, S1
Cho, CH1
Liu, S1
Lawson, KA1
Simmons-Menchaca, M1
Sun, L1
Sanders, BG1
Kline, K1
Li, N1
Sood, S1
Wang, S1
Fang, M1
Wang, P1
Sun, Z1
Yang, CS1
Chen, X1
Javle, MM1
Cao, S1
Durrani, FA1
Pendyala, L1
Lawrence, DD1
Smith, PF1
Creaven, PJ1
Noel, DC1
Iyer, RV1
Rustum, YM1
Masferrer, JL1
Leahy, KM1
Koki, AT1
Zweifel, BS1
Settle, SL1
Woerner, BM1
Edwards, DA1
Flickinger, AG1
Moore, RJ1
Seibert, K1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Radiosensitization With a COX-2 Inhibitor (Celecoxib), With Chemoradiation for Cancer of the Head and Neck[NCT00581971]Phase 1/Phase 230 participants (Actual)Interventional2002-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Response as Evaluated by Recurrence of Diseases

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)

InterventionParticipants (Number)
Local Control OnlyLocal Control and Distant MetastasisDistant Metastatsis OnlySecondary Primary - Site UnknownSurgical Salvage
Recurrence62123

Toxicity of Celecoxib With Concurrent Weekly Chemotherapy and Radiotherapy in the Treatment of Locally Advanced or Recurrent Squamous Cell Carcinoma of the Head and Neck.

Particpants experiencing Acute Toxicities > Grade 3 (NCT00581971)
Timeframe: 2 years from radiation therapy

Interventionparticipants (Number)
HematologicDermatitisMucositis/Dysphagia
Acute Toxicity12716

Trials

1 trial available for celecoxib and Experimental Neoplasms

ArticleYear
Celecoxib and mucosal protection: translation from an animal model to a phase I clinical trial of celecoxib, irinotecan, and 5-fluorouracil.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2007, Feb-01, Volume: 13, Issue:3

    Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Camptothecin; Celeco

2007

Other Studies

14 other studies available for celecoxib and Experimental Neoplasms

ArticleYear
Celecoxib Conjugated Fluorescent Probe for Identification and Discrimination of Cyclooxygenase-2 Enzyme in Cancer Cells.
    Analytical chemistry, 2018, 04-17, Volume: 90, Issue:8

    Topics: Animals; Celecoxib; Cell Survival; Cells, Cultured; Chlorocebus aethiops; Cyclooxygenase 2; Dose-Res

2018
Prophylactic intervention of probiotics (L.acidophilus, L.rhamnosus GG) and celecoxib modulate Bax-mediated apoptosis in 1,2-dimethylhydrazine-induced experimental colon carcinogenesis.
    BMC cancer, 2018, Nov-13, Volume: 18, Issue:1

    Topics: 1,2-Dimethylhydrazine; Animals; Apoptosis; bcl-2-Associated X Protein; Carcinogenesis; Carcinogens;

2018
A triple combination of atorvastatin, celecoxib and tipifarnib strongly inhibits pancreatic cancer cells and xenograft pancreatic tumors.
    International journal of oncology, 2014, Volume: 44, Issue:6

    Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Atorvasta

2014
Cyclooxygenase-2 inhibition as a strategy for treating gastric adenocarcinoma.
    Oncology reports, 2014, Volume: 32, Issue:3

    Topics: Adenocarcinoma; Animals; Celecoxib; Cell Line, Tumor; Cell Proliferation; Cyclooxygenase 2; Cyclooxy

2014
Modulation by licofelone and celecoxib of experimentally induced cancer and preneoplastic lesions in mice exposed to cigarette smoke.
    Current cancer drug targets, 2015, Volume: 15, Issue:3

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Anticarcinogenic Agents; Body Weight; Celecoxib; C

2015
Expression of Endoglin and Vascular Endothelial Growth Factor as Prognostic Markers in Experimental Colorectal Cancer.
    Anticancer research, 2016, Volume: 36, Issue:8

    Topics: Adenocarcinoma; Animals; Biomarkers, Tumor; Celecoxib; Colorectal Neoplasms; Cyclooxygenase 2 Inhibi

2016
Progressive metaplastic and dysplastic changes in mouse pancreas induced by cyclooxygenase-2 overexpression.
    Neoplasia (New York, N.Y.), 2008, Volume: 10, Issue:8

    Topics: Animals; Biomarkers, Tumor; Carcinoma, Pancreatic Ductal; Celecoxib; Cell Transformation, Neoplastic

2008
The human cytomegalovirus-encoded chemokine receptor US28 promotes angiogenesis and tumor formation via cyclooxygenase-2.
    Cancer research, 2009, Apr-01, Volume: 69, Issue:7

    Topics: Animals; Celecoxib; Cell Line; Cell Transformation, Viral; Cyclooxygenase 2; Cyclooxygenase 2 Inhibi

2009
Celecoxib prevents tumor growth in an animal model by a COX-2 independent mechanism.
    Cancer chemotherapy and pharmacology, 2010, Volume: 65, Issue:2

    Topics: Animals; Antineoplastic Agents; bcl-X Protein; Body Weight; Catalase; Celecoxib; Cyclooxygenase 2; C

2010
Cyclin D1 expression and the inhibitory effect of celecoxib on ovarian tumor growth in vivo.
    International journal of molecular sciences, 2010, Oct-19, Volume: 11, Issue:10

    Topics: Animals; Antineoplastic Agents; Apoptosis; Celecoxib; Cell Line, Tumor; Cell Proliferation; Cyclin D

2010
Celecoxib antagonizes the cytotoxicity of cisplatin in human esophageal squamous cell carcinoma cells by reducing intracellular cisplatin accumulation.
    Molecular pharmacology, 2011, Volume: 79, Issue:3

    Topics: Animals; Apoptosis; Blotting, Western; Carcinoma, Squamous Cell; Celecoxib; Cell Line, Tumor; Cispla

2011
Vitamin E analog alpha-TEA and celecoxib alone and together reduce human MDA-MB-435-FL-GFP breast cancer burden and metastasis in nude mice.
    Breast cancer research and treatment, 2004, Volume: 87, Issue:2

    Topics: Animals; Antineoplastic Agents; Breast Neoplasms; Celecoxib; Drug Interactions; Drug Therapy, Combin

2004
Overexpression of 5-lipoxygenase and cyclooxygenase 2 in hamster and human oral cancer and chemopreventive effects of zileuton and celecoxib.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2005, Mar-01, Volume: 11, Issue:5

    Topics: 9,10-Dimethyl-1,2-benzanthracene; Animals; Arachidonate 5-Lipoxygenase; Arachidonic Acid; Carcinogen

2005
Antiangiogenic and antitumor activities of cyclooxygenase-2 inhibitors.
    Cancer research, 2000, Mar-01, Volume: 60, Issue:5

    Topics: Animals; Anticarcinogenic Agents; Celecoxib; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxy

2000