Preprint Article Version 1 Preserved in Portico This version is not peer-reviewed

MicroRNAs within Basal-Like Signature of Quadruple Negative Breast Cancer Impact Overall Survival in African Americans

Version 1 : Received: 22 July 2022 / Approved: 27 July 2022 / Online: 27 July 2022 (04:07:32 CEST)

How to cite: Yates, C.; Angajala, A.; Muhammad, A.; Raymond, H.; Md Ahmed, S.; Haleema, S.; Haque, M.; Wang, H.; Martini, R.; Karanam, B.; G. Kahn, A.; Bedi, D.; Davis, M.; Tan, M.; Dean-Colomb, W. MicroRNAs within Basal-Like Signature of Quadruple Negative Breast Cancer Impact Overall Survival in African Americans. Preprints 2022, 2022070409. https://doi.org/10.20944/preprints202207.0409.v1 Yates, C.; Angajala, A.; Muhammad, A.; Raymond, H.; Md Ahmed, S.; Haleema, S.; Haque, M.; Wang, H.; Martini, R.; Karanam, B.; G. Kahn, A.; Bedi, D.; Davis, M.; Tan, M.; Dean-Colomb, W. MicroRNAs within Basal-Like Signature of Quadruple Negative Breast Cancer Impact Overall Survival in African Americans. Preprints 2022, 2022070409. https://doi.org/10.20944/preprints202207.0409.v1

Abstract

Background: We 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. Methods: Both miRNA and mRNA expression data were analyzed from TCGA and validated using datasets from the METABRIC, TCGA proteomic, and survival analysis by KMPLOT. Results: 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. Conclusion: Thus, QNBC tumors have an altered gene signature implicated in racial disparity and poor survival.

Keywords

QNBC (Quadruple negative breast cancer); AR (Androgen receptor); AA (African American); CA (Caucasian); BC (Breast cancer)

Subject

Biology and Life Sciences, Biochemistry and Molecular Biology

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