Human epidermal growth factor receptor 2–positive breast cancer is associated with Indigenous American ancestry in Latin American women
- COLUMBUS Consortium,
- Katie M. Marker(Author),
- Valentina A. Zavala(Author),
- Tatiana Vidaurre(Author),
- Paul C. Lott(Author),
- Jeannie Navarro Vásquez(Author)
- University of California, San Francisco,
- University of California Berkeley,
- Instituto Nacional de Enfermedades Neoplásicas,
- University of California Davis,
- ,
- Instituto Mexicano del Seguro Social
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Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 1893-1901 (9 pages)Journal (Volume, Issue Number)
Cancer Research (Volume 80, Issue 9)Publication milestones
- Published - 05/2020
Publication status
ISSN
0008-5472Publication IDs
- Scopus: 85085894437
- PubMed: 32245796
Abstract
Women of Latin American origin in the United States are more likely to be diagnosed with advanced breast cancer and have a higher risk of mortality than non-Hispanic White women. Studies in U.S. Latinas and Latin American women have reported a high incidence of HER2 positive (þ) tumors; however, the factors contributing to this observation are unknown. Genome-wide genotype data for 1,312 patients from the Peruvian Genetics and Genomics of Breast Cancer Study (PEGEN-BC) were used to estimate genetic ancestry. We tested the association between HER2 status and genetic ancestry using logistic and multinomial logistic regression models. Findings were replicated in 616 samples from Mexico and Colombia. Average Indigenous American (IA) ancestry differed by subtype. In multivariate models, the odds of having an HER2þ tumor increased by a factor of 1.20 with every 10% increase in IA ancestry proportion (95% CI, 1.07–1.35; P ¼ 0.001). The association between HER2 status and IA ancestry was independently replicated in samples from Mexico and Colombia. Results suggest that the high prevalence of HER2þ tumors in Latinas could be due in part to the presence of population-specific genetic variant(s) affecting HER2 expression in breast cancer.
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