The TRIM37 variant rs57141087 contributes to triple-negative breast cancer outcomes in Black women

Triple-negative breast cancer (TNBC) disproportionately affects younger Black women, who show more aggressive phenotypes and poorer outcomes than women of other racial identities. While the impact of socioenvironmental inequities within and beyond health systems is well documented, the genetic influence in TNBC-associated racial disparities remains elusive. Here, we report that cancer-free breast tissue from Black women expresses TRIM37 at a significantly higher level relative to White women. A reporter-based screen for regulatory variants identifies a non-coding risk variant rs57141087 in the 5' gene upstream region of the TRIM37 locus with enhancer activity. Mechanistically, rs57141087 increases enhancer-promoter interactions through NRF1, resulting in stronger TRIM37 promoter activity. Phenotypically, high TRIM37 levels drive neoplastic transformations in immortalized breast epithelial cells. Finally, context-dependent TRIM37 expression reveals that early-stage TRIM37 levels affect the initiation and trajectory of breast cancer progression. Together, our results indicate a genotype-informed association of oncogenic TRIM37 with TNBC risk in Black women and implicate TRIM37 as a predictive biomarker to better identify patients at risk of aggressive TNBC.

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Publication Details

Journal
EMBO Reports
Published
2024-11-29
DOI
https://doi.org/10.1038/s44319-024-00331-2
Citations
2
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.48

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article

The TRIM37 variant rs57141087 contributes to triple-negative breast cancer outcomes in Black women

Jogender Tushir‐Singh, Rachisan Djiake Tihagam, Xiaosong Huang, Sanchita Bhatnagar et al.
2 citations
EMBO Reports
interferon and immune responses
0.48
article

The TRIM37 variant rs57141087 contributes to triple-negative breast cancer outcomes in Black women

Jogender Tushir‐Singh, Rachisan Djiake Tihagam, Xiaosong Huang, Sanchita Bhatnagar, Piotr Przanowski, Bon Seok Koo, K. Liu, Laura Fejerman, Hong Li, Jie Li, Ankita Singh, Yuqi Zhao, Song Lou
article en
2 citations

Abstract

Triple-negative breast cancer (TNBC) disproportionately affects younger Black women, who show more aggressive phenotypes and poorer outcomes than women of other racial identities. While the impact of socioenvironmental inequities within and beyond health systems is well documented, the genetic influence in TNBC-associated racial disparities remains elusive. Here, we report that cancer-free breast tissue from Black women expresses TRIM37 at a significantly higher level relative to White women. A reporter-based screen for regulatory variants identifies a non-coding risk variant rs57141087 in the 5' gene upstream region of the TRIM37 locus with enhancer activity. Mechanistically, rs57141087 increases enhancer-promoter interactions through NRF1, resulting in stronger TRIM37 promoter activity. Phenotypically, high TRIM37 levels drive neoplastic transformations in immortalized breast epithelial cells. Finally, context-dependent TRIM37 expression reveals that early-stage TRIM37 levels affect the initiation and trajectory of breast cancer progression. Together, our results indicate a genotype-informed association of oncogenic TRIM37 with TNBC risk in Black women and implicate TRIM37 as a predictive biomarker to better identify patients at risk of aggressive TNBC.

EMBO ReportsVol. 26(1)
University of California Davis Medical Center (US), University of Virginia (US), University of California, Davis (US)
METAvivor, National Institutes of Health, University of California, Davis, School of Medicine, Indiana University, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institute on Drug Abuse, National Human Genome Research Institute, NIH Office of the Director, National Cancer Institute, National Institute of Neurological Disorders and Stroke, Common Fund
No poverty
Openalex Percentile: Top 33%
interferon and immune responses
0.48
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