mTOR pathway candidate genes and physical activity interaction on breast cancer risk in black women from the women's circle of health study

被引:0
作者
Ilozumba, Mmadili N. [1 ,2 ]
Yaghjyan, Lusine [1 ]
Datta, Susmita [3 ]
Zhao, Jinying [1 ]
Gong, Zhihong [4 ]
Hong, Chi-Chen [4 ]
Lunetta, Kathryn L. [5 ]
Zirpoli, Gary [6 ]
Bandera, Elisa V. [7 ]
Palmer, Julie R. [6 ]
Yao, Song [4 ]
Ambrosone, Christine B. [4 ]
Cheng, Ting-Yuan David [1 ,4 ,8 ]
机构
[1] Univ Florida, Dept Epidemiol, Gainesville, FL 32611 USA
[2] Univ Utah, Huntsman Canc Inst, Dept Populat Hlth Sci, 2000 Circle Hope, Salt Lake City, UT 84112 USA
[3] Univ Florida, Dept Biostat, Gainesville, FL USA
[4] Roswell Pk Comprehens Canc Ctr, Dept Canc Prevent & Control, Buffalo, NY 14203 USA
[5] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[6] Boston Univ, Slone Epidemiol Ctr, Boston, MA USA
[7] Rutgers Canc Inst New Jersey, Canc Epidemiol & Hlth Outcomes, New Brunswick, NJ USA
[8] Ohio State Univ, Dept Internal Med, Div Canc Prevent & Control, Suite 525 1590 North High St, Columbus, OH 43201 USA
基金
美国国家卫生研究院;
关键词
Physical activity; mTOR pathway; Breast cancer; Black women; Effect modification; AFRICAN-AMERICAN; MAMMALIAN TARGET; ENERGY-BALANCE; VARIANTS; ASSOCIATION; PHOSPHORYLATION; POPULATION; DOWNSTREAM; RAPAMYCIN; MEDIATE;
D O I
10.1007/s10549-023-06902-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPhysical activity has been shown to affect the mammalian target of rapamycin (mTOR) signaling pathway and consequently breast carcinogenesis. Given that Black women in the USA are less physically active, it is not well understood whether there are gene-environment interactions between mTOR pathway genes and physical activity in relation to breast cancer risk in Black women.MethodsThe study included 1398 Black women (567 incident breast cancer cases and 831 controls) from the Women's Circle of Health Study (WCHS). We examined interactions between 43 candidate single-nucleotide polymorphisms (SNPs) in 20 mTOR pathway genes with levels of vigorous physical activity in relation to breast cancer risk overall and by ER-defined subtypes using Wald test with 2-way interaction term and multivariable logistic regression.ResultsAKT1 rs10138227 (C > T) and AKT1 rs1130214 (C > A) were only associated with a decreased risk of ER + breast cancer among women with vigorous physical activity (odds ratio [OR] = 0.15, 95% confidence interval (CI) 0.04, 0.56, for each copy of the T allele, p-interaction = 0.007 and OR = 0.51, 95% CI 0.27, 0.96, for each copy of the A allele, p-interaction = 0.045, respectively). MTOR rs2295080 (G > T) was only associated with an increased risk of ER + breast cancer among women with vigorous physical activity (OR = 2.24, 95% CI 1.16, 4.34, for each copy of the G allele; p-interaction = 0.043). EIF4E rs141689493 (G > A) was only associated with an increased risk of ER- breast cancer among women with vigorous physical activity (OR = 20.54, 95% CI 2.29, 184.17, for each copy of the A allele; p-interaction = 0.003). These interactions became non-significant after correction for multiple testing (FDR-adjusted p-value > 0.05).ConclusionOur findings suggest that mTOR genetic variants may interact with physical activity in relation to breast cancer risk in Black women. Future studies should confirm these findings.
引用
收藏
页码:137 / 146
页数:10
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