Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes.
Dan ZhaoKerui WuSambad SharmaFei XingShih-Ying WuAbhishek TyagiRavindra DeshpandeRavi SinghMartin WabitschYin-Yuan MoKounosuke WatabePublished in: Nature communications (2022)
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.
Keyphrases
- african american
- end stage renal disease
- poor prognosis
- newly diagnosed
- chronic kidney disease
- cell proliferation
- long non coding rna
- prognostic factors
- genome wide
- healthcare
- peritoneal dialysis
- free survival
- transcription factor
- cardiovascular disease
- type diabetes
- risk assessment
- signaling pathway
- copy number
- young adults
- papillary thyroid
- patient reported
- lymph node metastasis
- genome wide identification
- childhood cancer
- squamous cell