Author:
Martini Rachel,Chen Yalei,Jenkins Brittany D.,Elhussin Isra A.,Cheng Esther,Hoda Syed A.,Ginter Paula S.,Hanover Jeffrey,Zeidan Rozina B.,Oppong Joseph K.,Adjei Ernest K.,Jibril Aisha,Chitale Dhananjay,Bensenhaver Jessica M.,Awuah Baffour,Bekele Mahteme,Abebe Engida,Kyei Ishmael,Aitpillah Frances S.,Adinku Michael O.,Ankomah Kwasi,Osei-Bonsu Ernest B.,Nathansan Saul David,Jackson LaToya,Jiagge Evelyn,Petersen Lindsay F.,Proctor Erica,Nikolinakos Petros,Gyan Kofi K.,Yates Clayton,Kittles Rick,Newman Lisa A.,Davis Melissa B.
Abstract
AbstractLarge-scale efforts to identify breast cancer (BC) risk alleles have historically taken place among women of European ancestry. Recently, there are new efforts to verify if these alleles increase risk in African American (AA) women as well. We investigated the effect of previously reported AA breast cancer and triple-negative breast cancer (TNBC) risk alleles in our African-enriched International Center for the Study of Breast Cancer Subtypes (ICSBCS) cohort. Using case–control, case-series and race-nested approaches, we report that the Duffy-null allele (rs2814778) is associated with TNBC risk (OR = 3.814, p = 0.001), specifically among AA individuals, after adjusting for self-indicated race and west African ancestry (OR = 3.368, p = 0.007). We have also validated the protective effect of the minor allele of the ANKLE1 missense variant rs2363956 among AA for TNBC (OR = 0.420, p = 0.005). Our results suggest that an ancestry-specific Duffy-null allele and differential prevalence of a polymorphic gene variant of ANKLE1 may play a role in TNBC breast cancer outcomes. These findings present opportunities for therapeutic potential and future studies to address race-specific differences in TNBC risk and disease outcome.
Funder
National Institute on Minority Health and Health Disparities
National Cancer Institute
Susan G. Komen
Fashion Footwear Association of New York
Publisher
Springer Science and Business Media LLC
Cited by
14 articles.
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