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乳腺癌生存种族差异的基因组和社会经济决定因素:来自“我们所有人”计划的见解。

Genomic and Socioeconomic Determinants of Racial Disparities in Breast Cancer Survival: Insights from the All of Us Program.

作者信息

Rizvi Nubaira, Lyu Hui, Vaidya Leah, Wu Xiao-Cheng, Miele Lucio, Yu Qingzhao

机构信息

Biostatistics and Data Science, School of Public Health, LSU Health-New Orleans, New Orleans, LA 70112, USA.

Department of Interdisciplinary Oncology, LSU Health-New Orleans, New Orleans, LA 70112, USA.

出版信息

Cancers (Basel). 2024 Sep 27;16(19):3294. doi: 10.3390/cancers16193294.

DOI:10.3390/cancers16193294
PMID:39409914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11475812/
Abstract

: Breast cancer outcomes are worse among Black women in the U.S. compared to White women. While extensive research has focused on risk factors contributing to breast cancer; the role of genomic elements in health disparities between these racial groups remains unclear. This study aims to identify genomic variants and socioeconomic status (SES) determinants influencing racial disparities in breast cancer survival through multiple mediation analyses. : Our investigation is based on the NIH-supported All of Us (AoU) program and analyzes 7452 female participants with malignant tumors of breast, including 5073 with genomic data. A log-rank test reveals significant racial differences in overall survival time between Black and White participants (-value = 0.04). Multiple mediation analysis examines the effects of 9481 genetic variables across 23 chromosomes in explaining the racial disparity in survival, adjusting for SES variables. : 15 gene mutations, in addition to age, general health, and general quality of life, have significant effects (-values < 0.001) in explaining the observed racial disparity. Mutations in TMEM132B, NARFL, SALL1, PAD12, RIPK1, ASB14, DCX, GNB1L, ARHGAP32, AL135787.1, WBP11, SLC16A12AS1, AP000345.1, IKBKB, and SUPT20H have significantly different distributions between Black and White participants. The disparity is completely explained by the included variables as the direct effect is insignificant (-value = 0.73). : The combined impact of SES determinants and genetic mutations can explain the observed differences in breast cancer survival among Black and White participants. Future studies will explore pathways and design in vivo and in vitro experiments to validate the functions of these genes.

摘要

与美国白人女性相比,美国黑人女性的乳腺癌预后更差。虽然广泛的研究集中在导致乳腺癌的风险因素上,但这些种族群体之间健康差异中基因组因素的作用仍不清楚。本研究旨在通过多重中介分析确定影响乳腺癌生存种族差异的基因组变异和社会经济地位(SES)决定因素。

我们的调查基于美国国立卫生研究院支持的“我们所有人(AoU)”项目,分析了7452名患有乳腺恶性肿瘤的女性参与者,其中5073名有基因组数据。对数秩检验显示黑人和白人参与者的总生存时间存在显著种族差异(P值 = 0.04)。多重中介分析检验了23条染色体上9481个基因变量在解释生存种族差异方面的作用,并对SES变量进行了调整。

除年龄、总体健康状况和总体生活质量外,15个基因突变在解释观察到的种族差异方面具有显著影响(P值 < 0.001)。TMEM132B、NARFL、SALL1、PAD12、RIPK1、ASB14、DCX、GNB1L、ARHGAP32、AL135787.1、WBP11、SLC16A12AS1、AP000345.1、IKBKB和SUPT20H的突变在黑人和白人参与者之间的分布存在显著差异。由于直接效应不显著(P值 = 0.73),所纳入的变量完全解释了这种差异。

SES决定因素和基因突变的综合影响可以解释观察到的黑人和白人参与者在乳腺癌生存方面的差异。未来的研究将探索相关途径,并设计体内和体外实验来验证这些基因的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/4593ba113cff/cancers-16-03294-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/07889bc535d5/cancers-16-03294-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/913f00cf9f51/cancers-16-03294-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/4593ba113cff/cancers-16-03294-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/07889bc535d5/cancers-16-03294-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/913f00cf9f51/cancers-16-03294-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9709/11475812/4593ba113cff/cancers-16-03294-g004.jpg

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