Associations of aspirin and other anti-inflammatory medications with breast cancer risk by the status of COX-2 expression

被引:3
|
作者
Yaghjyan, Lusine [1 ,2 ]
Eliassen, A. Heather [3 ]
Colditz, Graham [4 ,5 ]
Rosner, Bernard [3 ]
Schedin, Pepper [6 ]
Wijayabahu, Akemi [1 ,2 ]
Tamimi, Rulla M. [7 ]
机构
[1] Univ Florida, Coll Publ Hlth & Hlth Profess, Dept Epidemiol, 2004 Mowry Rd, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, 2004 Mowry Rd, Gainesville, FL 32610 USA
[3] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Channing Div Network Med, Boston, MA USA
[4] Washington Univ St Louis, Sch Med, Dept Surg, St Louis, MO USA
[5] Washington Univ St Louis, Inst Publ Hlth, St Louis, MO USA
[6] Oregon Hlth & Sci Univ, Portland, OR USA
[7] Weill Cornell Med, Dept Populat Hlth Sci, New York, NY USA
基金
美国国家卫生研究院;
关键词
Breast cancer risk; Aspirin; COX-2; NSAIDs; MAMMOGRAPHIC DENSITY; SUBSEQUENT RISK; NURSES HEALTH; DRUGS; WOMEN; ACETAMINOPHEN;
D O I
10.1186/s13058-022-01575-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Survivin and COX-2 expression in male breast cancer
    Younis, T.
    Dakin-Hache, K. A.
    Rayson, D.
    Dewar, R.
    Gray, S.
    Barnes, P. J.
    BREAST CANCER RESEARCH AND TREATMENT, 2007, 106 : S222 - S222
  • [42] COX-2/5-LOX dual acting anti-inflammatory drugs in cancer chemotherapy
    Goossens, Laurence
    Pommery, Nicole
    Henichart, Jean Pierre
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2007, 7 (03) : 283 - 296
  • [43] Cox-2 expression on tissue microarray of breast cancer
    Park, K.
    Han, S.
    Shin, E.
    Kim, H. -J.
    Kim, J. -Y.
    EJSO, 2006, 32 (10): : 1093 - 1096
  • [44] Cardiovascular risk of selective cyclooxygenase-2 inhibitors and other non-aspirin non-steroidal anti-inflammatory medications
    Velentgas, P
    West, W
    Cannuscio, CC
    Watson, DJ
    Walker, AM
    CIRCULATION, 2005, 111 (14) : E226 - E226
  • [45] The effects of aspirin on growth and COX-2 expression in prostate cancer cells
    Wang, R.
    Shah, U. K.
    Jenkins, G.
    Doak, S.
    EUROPEAN JOURNAL OF CANCER, 2016, 61 : S41 - S41
  • [46] Expression of cyclooxygenase-2(Cox-2) in breast tumors and Inhibition of Cox-2 by Genistein in Breast cancer.
    Yoon, DS
    Kim, YM
    Song, KH
    Kim, ST
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2003, 12 (11) : 1348S - 1348S
  • [47] Significant expression of Cox-2 according to Aromatase, independent on ER status: implications to breast cancer therapy with Aromatase and Cox-2 inhibitors
    Ragaz, J
    Bajdik, C
    Spinelli, JJ
    Hayes, A
    Jelacic, D
    Brodie, A
    BREAST CANCER RESEARCH AND TREATMENT, 2004, 88 : S22 - S23
  • [48] Risk of hospitalization for angio-oedema among users of newer COX-2 selective inhibitors and other nonsteroidal anti-inflammatory drugs
    Downing, Amy
    Jacobsen, Jacob
    Sorensen, Henrik T.
    McLaughlin, Joseph K.
    Johnsen, Soren P.
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 62 (04) : 496 - 501
  • [49] Design of balanced COX inhibitors based on anti-inflammatory and/or COX-2 inhibitory ascidian metabolites
    Ju, Zhiran
    Su, Mingzhi
    Hong, Jongki
    Kim, Eun La
    Moon, Hyung Ryong
    Chung, Hae Young
    Kim, Suhkmann
    Jung, Jee H.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2019, 180 : 86 - 98
  • [50] Anti-inflammatory function of arctiin by inhibiting COX-2 expression via NF-κB pathways
    Sungwon Lee
    Seulmee Shin
    Hyunyul Kim
    Shinha Han
    Kwanghee Kim
    Jeunghak Kwon
    Jin-Hwan Kwak
    Chong-Kil Lee
    Nam-Joo Ha
    Dongsool Yim
    Kyungjae Kim
    Journal of Inflammation, 8