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饮食和生活方式因素与丝裂原活化蛋白激酶(MAPK)基因相互作用以影响生存:乳腺癌健康差异研究。

Diet and lifestyle factors interact with MAPK genes to influence survival: the Breast Cancer Health Disparities Study.

作者信息

Slattery Martha L, Hines Lisa H, Lundgreen Abbie, Baumgartner Kathy B, Wolff Roger K, Stern Mariana C, John Esther M

机构信息

Department of Medicine, University of Utah, 383 Colorow, Salt Lake City, UT, 84108, USA,

出版信息

Cancer Causes Control. 2014 Sep;25(9):1211-25. doi: 10.1007/s10552-014-0426-y. Epub 2014 Jul 4.

Abstract

INTRODUCTION

MAPK genes are activated by a variety of factors related to growth factors, hormones, and environmental stress.

METHODS

We evaluated associations between 13 MAPK genes and survival among 1,187 nonHispanic White and 1,155 Hispanic/Native American (NA) women diagnosed with breast cancer. We assessed the influence of diet, lifestyle, and genetic ancestry on these associations. Percent NA ancestry was determined from 104 Ancestry Informative Markers. Adaptive rank truncation product (ARTP) was used to determine gene and pathway significance.

RESULTS

Associations were predominantly observed among women with lower NA ancestry. Specifically, the mitogen-activated protein kinases (MAPK) pathway was associated with all-cause mortality (P ARTP = 0.02), but not with breast cancer-specific mortality (P ARTP = 0.10). However, MAP2K1 and MAP3K9 were associated with both breast cancer-specific and all-cause mortality. MAPK12 (P ARTP = 0.05) was only associated with breast cancer-specific mortality, and MAP3K1 (P ARTP = 0.02) and MAPK1 (P ARTP = 0.05) were only associated with all-cause mortality. Among women with higher NA ancestry, MAP3K2 was significantly associated with all-cause mortality (P ARTP = 0.04). Several diet and lifestyle factors, including alcohol consumption, caloric intake, dietary folate, and cigarette smoking, significantly modified the associations with MAPK genes and all-cause mortality.

CONCLUSIONS

Our study supports an association between MAPK genes and survival after diagnosis with breast cancer, especially among women with low NA ancestry. The interaction between genetic variation in the MAPK pathway with diet and lifestyle factors for all women supports the important role of these factors for breast cancer survivorship.

摘要

引言

丝裂原活化蛋白激酶(MAPK)基因可被多种与生长因子、激素及环境应激相关的因素激活。

方法

我们评估了13个MAPK基因与1187名非西班牙裔白人及1155名西班牙裔/美洲原住民(NA)乳腺癌女性患者生存率之间的关联。我们评估了饮食、生活方式和遗传血统对这些关联的影响。通过104个祖先信息标记确定NA血统百分比。采用适应性秩截断乘积(ARTP)来确定基因和通路的显著性。

结果

主要在NA血统较低的女性中观察到关联。具体而言,丝裂原活化蛋白激酶(MAPK)通路与全因死亡率相关(P ARTP = 0.02),但与乳腺癌特异性死亡率无关(P ARTP = 0.10)。然而,MAP2K1和MAP3K9与乳腺癌特异性死亡率和全因死亡率均相关。MAPK12(P ARTP = 0.05)仅与乳腺癌特异性死亡率相关,而MAP3K1(P ARTP = 0.02)和MAPK1(P ARTP = 0.05)仅与全因死亡率相关。在NA血统较高的女性中,MAP3K2与全因死亡率显著相关(P ARTP = 0.04)。包括饮酒、热量摄入、膳食叶酸和吸烟在内的几种饮食和生活方式因素,显著改变了与MAPK基因和全因死亡率的关联。

结论

我们的研究支持MAPK基因与乳腺癌诊断后生存率之间的关联,尤其是在NA血统较低的女性中。MAPK通路基因变异与所有女性饮食和生活方式因素之间的相互作用,支持了这些因素对乳腺癌生存的重要作用。

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