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Published in: BMC Cancer 1/2008

Open Access 01-12-2008 | Research article

Celecoxib concentration predicts decrease in prostaglandin E2concentrations in nipple aspirate fluid from high risk women

Authors: Edward R Sauter, Wenyi Qin, John E Hewett, Rachel L Ruhlen, John T Flynn, George Rottinghaus, Yin-Chieh Chen

Published in: BMC Cancer | Issue 1/2008

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Abstract

Background

Epidemiologic studies suggest that long term low dose celecoxib use significantly lowers breast cancer risk. We previously demonstrated that 400 mg celecoxib taken twice daily for 2 weeks lowered circulating plasma and breast nipple aspirate fluid (NAF) prostaglandin (PG)E2 concentrations in post- but not premenopausal high risk women. We hypothesized that circulating concentrations of celecoxib influenced PGE2 response, and that plasma levels of the drug are influenced by menopausal status. To address these hypotheses, the aims of the study were to determine: 1) if circulating plasma concentrations of celecoxib correlated with the change in plasma or NAF PGE2 concentrations from baseline to end of treatment, and 2) whether menopausal status influenced circulating levels of celecoxib.

Methods

Matched NAF and plasma were collected from 46 high risk women who were administered celecoxib twice daily for two weeks, 20 subjects receiving 200 mg and 26 subjects 400 mg of the agent. NAF and plasma samples were collected before and 2 weeks after taking celecoxib.

Results

In women taking 400 mg bid celecoxib, plasma concentrations of the agent correlated inversely with the change in NAF PGE2 levels from pre- to posttreatment. Nonsignificant trends toward higher celecoxib levels were observed in post- compared to premenopausal women. There was a significant decrease in NAF but not plasma PGE2 concentrations in postmenopausal women who took 400 mg celecoxib (p = 0.03).

Conclusion

In high risk women taking 400 mg celecoxib twice daily, plasma concentrations of celecoxib correlated with downregulation of PGE2 production by breast tissue. Strategies synergistic with celecoxib to downregulate PGE2 are of interest, in order to minimize the celecoxib dose required to have an effect.
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Literature
1.
go back to reference Whittle BJ: Gastrointestinal effects of nonsteroidal anti-inflammatory drugs. Fundam Clin Pharmacol. 2003, 17 (3): 301-313. 10.1046/j.1472-8206.2003.00135.x.CrossRefPubMed Whittle BJ: Gastrointestinal effects of nonsteroidal anti-inflammatory drugs. Fundam Clin Pharmacol. 2003, 17 (3): 301-313. 10.1046/j.1472-8206.2003.00135.x.CrossRefPubMed
2.
go back to reference Masferrer JL, Leahy KM, Koki AT, Zweifel BS, Settle SL, Woerner BM, Edwards DA, Flickinger AG, Moore RJ, Seibert K: Antiangiogenic and antitumor activities of cyclooxygenase-2 inhibitors. Cancer Res. 2000, 60 (5): 1306-1311.PubMed Masferrer JL, Leahy KM, Koki AT, Zweifel BS, Settle SL, Woerner BM, Edwards DA, Flickinger AG, Moore RJ, Seibert K: Antiangiogenic and antitumor activities of cyclooxygenase-2 inhibitors. Cancer Res. 2000, 60 (5): 1306-1311.PubMed
3.
go back to reference Taketo MM: Cyclooxygenase-2 inhibitors in tumorigenesis (Part II). J Natl Cancer Inst. 1998, 90 (21): 1609-1620. 10.1093/jnci/90.21.1609.CrossRefPubMed Taketo MM: Cyclooxygenase-2 inhibitors in tumorigenesis (Part II). J Natl Cancer Inst. 1998, 90 (21): 1609-1620. 10.1093/jnci/90.21.1609.CrossRefPubMed
4.
go back to reference Fulton AM, Gimotty P, Alonsozana E, Dorsey R, Kundu N: Elevated prostaglandin E2 (PGE2) levels in human breast cancer are associated with poor long-term survival. Proc Am Assn Cancer Res. 2000, 41: 3660A- Fulton AM, Gimotty P, Alonsozana E, Dorsey R, Kundu N: Elevated prostaglandin E2 (PGE2) levels in human breast cancer are associated with poor long-term survival. Proc Am Assn Cancer Res. 2000, 41: 3660A-
5.
go back to reference Meagher EA: Balancing gastroprotection and cardioprotection with selective cyclo-oxygenase-2 inhibitors: clinical implications. Drug Saf. 2003, 26 (13): 913-924. 10.2165/00002018-200326130-00001.CrossRefPubMed Meagher EA: Balancing gastroprotection and cardioprotection with selective cyclo-oxygenase-2 inhibitors: clinical implications. Drug Saf. 2003, 26 (13): 913-924. 10.2165/00002018-200326130-00001.CrossRefPubMed
6.
go back to reference Abou-Issa HM, Alshafie GA, Seibert K, Koki AT, Masferrer JL, Harris RE: Dose-response effects of the COX-2 inhibitor, celecoxib, on the chemoprevention of mammary carcinogenesis. Anticancer Res. 2001, 21 (5): 3425-3432.PubMed Abou-Issa HM, Alshafie GA, Seibert K, Koki AT, Masferrer JL, Harris RE: Dose-response effects of the COX-2 inhibitor, celecoxib, on the chemoprevention of mammary carcinogenesis. Anticancer Res. 2001, 21 (5): 3425-3432.PubMed
7.
go back to reference Alshafie G, Abou-Issa HM, Seibert K, Harris RE: Chemotherapeutic evaluation of celecoxib, a cyclooxygenase-2 (COX-2) inhibitor, in a rat mammary tumor model. Oncol Rep. 2000, 7 (6): 1377-81.PubMed Alshafie G, Abou-Issa HM, Seibert K, Harris RE: Chemotherapeutic evaluation of celecoxib, a cyclooxygenase-2 (COX-2) inhibitor, in a rat mammary tumor model. Oncol Rep. 2000, 7 (6): 1377-81.PubMed
8.
go back to reference Harris RE, Beebe-Donk J, Alshafie GA: Reduction in the risk of human breast cancer by selective cyclooxygenase-2 (COX-2) inhibitors. BMC Cancer. 2006, 6: 27-10.1186/1471-2407-6-27.CrossRefPubMedPubMedCentral Harris RE, Beebe-Donk J, Alshafie GA: Reduction in the risk of human breast cancer by selective cyclooxygenase-2 (COX-2) inhibitors. BMC Cancer. 2006, 6: 27-10.1186/1471-2407-6-27.CrossRefPubMedPubMedCentral
9.
go back to reference Lanza-Jacoby S, Miller S, Flynn J, Gallatig K, Daskalakis C, Masferrer JL, Zweifel BS, Sembhi H, Russo IH: The cyclooxygenase-2 inhibitor, celecoxib, prevents the development of mammary tumors in Her-2/neu mice. Cancer Epidemiol Biomarkers Prev. 2003, 12 (12): 1486-1491.PubMed Lanza-Jacoby S, Miller S, Flynn J, Gallatig K, Daskalakis C, Masferrer JL, Zweifel BS, Sembhi H, Russo IH: The cyclooxygenase-2 inhibitor, celecoxib, prevents the development of mammary tumors in Her-2/neu mice. Cancer Epidemiol Biomarkers Prev. 2003, 12 (12): 1486-1491.PubMed
10.
go back to reference Cervi D, Klement G, Stempak D, Baruchel S, Koki A, Ben-David Y: Targeting cyclooxygenase-2 reduces overt toxicity toward low-dose vinblastine and extends survival of juvenile mice with Friend disease. Clin Cancer Res. 2005, 11 (2 Pt 1): 712-719.PubMed Cervi D, Klement G, Stempak D, Baruchel S, Koki A, Ben-David Y: Targeting cyclooxygenase-2 reduces overt toxicity toward low-dose vinblastine and extends survival of juvenile mice with Friend disease. Clin Cancer Res. 2005, 11 (2 Pt 1): 712-719.PubMed
11.
go back to reference Williams CS, Watson AJ, Sheng H, Helou R, Shao J, DuBois RN: Celecoxib prevents tumor growth in vivo without toxicity to normal gut: lack of correlation between in vitro and in vivo models. Cancer Res. 2000, 60 (21): 6045-6051.PubMed Williams CS, Watson AJ, Sheng H, Helou R, Shao J, DuBois RN: Celecoxib prevents tumor growth in vivo without toxicity to normal gut: lack of correlation between in vitro and in vivo models. Cancer Res. 2000, 60 (21): 6045-6051.PubMed
12.
go back to reference Hale TW, McDonald R, Boger J: Transfer of celecoxib into human milk. J Hum Lact. 2004, 20 (4): 397-403. 10.1177/0890334404269875.CrossRefPubMed Hale TW, McDonald R, Boger J: Transfer of celecoxib into human milk. J Hum Lact. 2004, 20 (4): 397-403. 10.1177/0890334404269875.CrossRefPubMed
13.
go back to reference Chow HH, Anavy N, Salazar D, Frank DH, Alberts DS: Determination of celecoxib in human plasma using solid-phase extraction and high-performance liquid chromatography. J Pharm Biomed Anal. 2004, 34 (1): 167-174. 10.1016/j.japna.2003.08.018.CrossRefPubMed Chow HH, Anavy N, Salazar D, Frank DH, Alberts DS: Determination of celecoxib in human plasma using solid-phase extraction and high-performance liquid chromatography. J Pharm Biomed Anal. 2004, 34 (1): 167-174. 10.1016/j.japna.2003.08.018.CrossRefPubMed
14.
go back to reference Sauter ER, Ross E, Daly M, Klein-Szanto A, Engstrom PF, Sorling A, Malick J, Ehya H: Nipple aspirate fluid: a promising non-invasive method to identify cellular markers of breast cancer risk. Br J Cancer. 1997, 76 (4): 494-501.CrossRefPubMedPubMedCentral Sauter ER, Ross E, Daly M, Klein-Szanto A, Engstrom PF, Sorling A, Malick J, Ehya H: Nipple aspirate fluid: a promising non-invasive method to identify cellular markers of breast cancer risk. Br J Cancer. 1997, 76 (4): 494-501.CrossRefPubMedPubMedCentral
15.
go back to reference Sauter ER, Schlatter L, Hewett J, Koivunen D, Flynn JT: Lack of effect of celecoxib on prostaglandin E2 concentrations in nipple aspirate fluid from women at increased risk of breast cancer. Cancer Epidemiol Biomarkers Prev. 2004, 13 (11 Pt 1): 1745-1750.PubMed Sauter ER, Schlatter L, Hewett J, Koivunen D, Flynn JT: Lack of effect of celecoxib on prostaglandin E2 concentrations in nipple aspirate fluid from women at increased risk of breast cancer. Cancer Epidemiol Biomarkers Prev. 2004, 13 (11 Pt 1): 1745-1750.PubMed
16.
go back to reference Sauter ER, Qin W, Schlatter L, Hewett JE, Flynn JT: Celecoxib decreases prostaglandin E2 concentrations in nipple aspirate fluid from high risk postmenopausal women and women with breast cancer. BMC Cancer. 2006, 6: 248-10.1186/1471-2407-6-248.CrossRefPubMedPubMedCentral Sauter ER, Qin W, Schlatter L, Hewett JE, Flynn JT: Celecoxib decreases prostaglandin E2 concentrations in nipple aspirate fluid from high risk postmenopausal women and women with breast cancer. BMC Cancer. 2006, 6: 248-10.1186/1471-2407-6-248.CrossRefPubMedPubMedCentral
17.
go back to reference Sauter ER, Daly M, Linahan K, Ehya H, Engstrom PF, Bonney G, Ross EA, Yu H, Diamandis E: Prostate-specific antigen levels in nipple aspirate fluid correlate with breast cancer risk. Cancer Epidemiol Biomarkers Prev. 1996, 5 (12): 967-970.PubMed Sauter ER, Daly M, Linahan K, Ehya H, Engstrom PF, Bonney G, Ross EA, Yu H, Diamandis E: Prostate-specific antigen levels in nipple aspirate fluid correlate with breast cancer risk. Cancer Epidemiol Biomarkers Prev. 1996, 5 (12): 967-970.PubMed
18.
go back to reference Schonberger F, Heinkele G, Murdter TE, Brenner S, Klotz U, Hofmann U: Simple and sensitive method for the determination of celecoxib in human serum by high-performance liquid chromatography with fluorescence detection. J Chromatogr B Analyt Technol Biomed Life Sci. 2002, 768 (2): 255-260. 10.1016/S1570-0232(01)00588-8.CrossRefPubMed Schonberger F, Heinkele G, Murdter TE, Brenner S, Klotz U, Hofmann U: Simple and sensitive method for the determination of celecoxib in human serum by high-performance liquid chromatography with fluorescence detection. J Chromatogr B Analyt Technol Biomed Life Sci. 2002, 768 (2): 255-260. 10.1016/S1570-0232(01)00588-8.CrossRefPubMed
19.
go back to reference Brenner SS, Herrlinger C, Dilger K, Murdter TE, Hofmann U, Marx C, Klotz U: Influence of age and cytochrome P450 2C9 genotype on the steady-state disposition of diclofenac and celecoxib. Clin Pharmacokinet. 2003, 42 (3): 283-292. 10.2165/00003088-200342030-00003.CrossRefPubMed Brenner SS, Herrlinger C, Dilger K, Murdter TE, Hofmann U, Marx C, Klotz U: Influence of age and cytochrome P450 2C9 genotype on the steady-state disposition of diclofenac and celecoxib. Clin Pharmacokinet. 2003, 42 (3): 283-292. 10.2165/00003088-200342030-00003.CrossRefPubMed
Metadata
Title
Celecoxib concentration predicts decrease in prostaglandin E2concentrations in nipple aspirate fluid from high risk women
Authors
Edward R Sauter
Wenyi Qin
John E Hewett
Rachel L Ruhlen
John T Flynn
George Rottinghaus
Yin-Chieh Chen
Publication date
01-12-2008
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2008
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/1471-2407-8-49

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