Abstract
Breast cancer displays disparities in mortality between African Americans and Caucasian Americans. However, the exact molecular mechanisms remain elusive. Here, we identify miR-1304-3p as the most upregulated microRNA in African American patients. Importantly, its expression significantly correlates with poor progression-free survival in African American patients. Ectopic expression of miR-1304 promotes tumor progression in vivo. Exosomal miR-1304-3p activates cancer-associated adipocytes that release lipids and enhance cancer cell growth. Moreover, we identify the anti-adipogenic gene GATA2 as the target of miR-1304-3p. Notably, a single nucleotide polymorphism (SNP) located in the miR-1304 stem-loop region shows a significant difference in frequencies of the G allele between African and Caucasian American groups, which promotes the maturation of miR-1304-3p. Therefore, our results reveal a mechanism of the disparity in breast cancer progression and suggest a potential utility of miR-1304-3p and the associated SNP as biomarkers for predicting the outcome of African American patients.
Original language | American English |
---|---|
Article number | 7734 |
Journal | Nature Communications |
Volume | 13 |
Issue number | 1 |
DOIs | |
State | Published - 2022 |
Externally published | Yes |
Fingerprint
Dive into the research topics of 'Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes'. Together they form a unique fingerprint.Equipment
-
Biosample Repository Facility
Connolly, PhD, D. (Director) & James, J. D. (Manager)
Equipment/facility: Facility