Author:
Angajala Anusha,Raymond Hughley,Muhammad Aliyu,Uddin Ahmed Md Shakir,Haleema Saadia,Haque Monira,Wang Honghe,Campbell Moray,Martini Rachel,Karanam Balasubramanian,Kahn Andrea G.,Bedi Deepa,Davis Melissa,Tan Ming,Dean-Colomb Windy,Yates Clayton
Abstract
AbstractWe previously found that QNBC tumors are more frequent in African Americans compared to TNBC tumors. To characterize this subtype further, we sought to determine the miRNA–mRNA profile in QNBC patients based on race. Both miRNA and mRNA expression data were analyzed from TCGA and validated using datasets from the METABRIC, TCGA proteomic, and survival analysis by KMPLOT. miRNA–mRNAs which include FOXA1 and MYC (mir-17/20a targets); GATA3 and CCNG2 (mir-135b targets); CDKN2A, CDK6, and B7-H3 (mir-29c targets); and RUNX3, KLF5, IL1-β, and CTNNB1 (mir-375 targets) were correlated with basal-like and immune subtypes in QNBC patients and associated with a worse survival. Thus, QNBC tumors have an altered gene signature implicated in racial disparity and poor survival.
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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