TY - JOUR
T1 - Associations of aspirin and other anti-inflammatory medications with breast cancer risk by the status of COX-2 expression
AU - Yaghjyan, Lusine
AU - Eliassen, A. Heather
AU - Colditz, Graham
AU - Rosner, Bernard
AU - Schedin, Pepper
AU - Wijayabahu, Akemi
AU - Tamimi, Rulla M.
N1 - Funding Information:
This work was supported by the National Cancer Institute at the National Institutes of Health [CA131332, CA175080, P01 CA087969 to R.M.T., UM1 CA186107 A.H.E., U01 CA176726 to W.W], Avon Foundation for Women, Susan G. Komen for the Cure®, and Breast Cancer Research Foundation.
Funding Information:
This work was supported by the National Cancer Institute at the National Institutes of Health [CA131332, CA175080, P01 CA087969 to R.M.T., UM1 CA186107 A.H.E., U01 CA176726 to W.W], Avon Foundation for Women, Susan G. Komen for the Cure®, and Breast Cancer Research Foundation. We would like to thank the participants and staff of the NHS and NHSII for their valuable contributions as well as the following state cancer registries for their help: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KY, LA, ME, MD, MA, MI, NE, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, WY. The authors assume full responsibility for analyses and interpretation of these data.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: We investigated the associations of aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) with breast cancer risk by the status of COX-2 protein expression. Methods: This study included 421 cases and 3,166 controls from a nested case–control study within the Nurses’ Health Study (NHS) and Nurses’ Health Study II (NHSII) cohorts. Information on medication use was first collected in 1980 (NHS) and 1989 (NHSII) and was updated biennially. Medication use was defined as none, past or current; average cumulative dose and frequency were calculated for all past or current users using data collected from all biannual questionnaires preceding the reference date. Immunochemistry for COX-2 expression was performed using commercial antibody (Cayman Chemical and Thermo Fisher Scientific). We used polychotomous logistic regression to quantify associations of aspirin and NSAIDs with the risk of COX2+ and COX2− breast cancer tumors, while adjusting for known breast cancer risk factors. All tests of statistical significance were two-sided. Results: In multivariate analysis, we found no differences in associations of the aspirin exposures and NSAIDs with breast cancer risk by COX2 expression status. In stratified analyses by COX2 status, significant associations of these medications with breast cancer risk were observed for dosage of aspirin among current users in COX2- tumors (OR for > 5 tablets per week vs. none 1.71, 95% CI 1.01–2.88, p-trend 0.04). Regular aspirin use was marginally associated with the risk of COX2- tumors (p-trend = 0.06). Conclusions: Our findings suggested no differences in associations of aspirin and other NSAIDs with COX2+ and COX2− tumors.
AB - Background: We investigated the associations of aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) with breast cancer risk by the status of COX-2 protein expression. Methods: This study included 421 cases and 3,166 controls from a nested case–control study within the Nurses’ Health Study (NHS) and Nurses’ Health Study II (NHSII) cohorts. Information on medication use was first collected in 1980 (NHS) and 1989 (NHSII) and was updated biennially. Medication use was defined as none, past or current; average cumulative dose and frequency were calculated for all past or current users using data collected from all biannual questionnaires preceding the reference date. Immunochemistry for COX-2 expression was performed using commercial antibody (Cayman Chemical and Thermo Fisher Scientific). We used polychotomous logistic regression to quantify associations of aspirin and NSAIDs with the risk of COX2+ and COX2− breast cancer tumors, while adjusting for known breast cancer risk factors. All tests of statistical significance were two-sided. Results: In multivariate analysis, we found no differences in associations of the aspirin exposures and NSAIDs with breast cancer risk by COX2 expression status. In stratified analyses by COX2 status, significant associations of these medications with breast cancer risk were observed for dosage of aspirin among current users in COX2- tumors (OR for > 5 tablets per week vs. none 1.71, 95% CI 1.01–2.88, p-trend 0.04). Regular aspirin use was marginally associated with the risk of COX2- tumors (p-trend = 0.06). Conclusions: Our findings suggested no differences in associations of aspirin and other NSAIDs with COX2+ and COX2− tumors.
KW - Aspirin
KW - Breast cancer risk
KW - COX-2
KW - NSAIDs
UR - http://www.scopus.com/inward/record.url?scp=85143626368&partnerID=8YFLogxK
U2 - 10.1186/s13058-022-01575-3
DO - 10.1186/s13058-022-01575-3
M3 - Article
C2 - 36494710
AN - SCOPUS:85143626368
SN - 1465-5411
VL - 24
JO - Breast Cancer Research
JF - Breast Cancer Research
IS - 1
M1 - 89
ER -