Faculty, Staff and Student Publications
Publication Date
1-1-2017
Journal
Cancer Discovery
DOI
10.1038/celldisc.2017.29
PMID
28904816
PMCID
PMC5594916
PubMedCentral® Posted Date
9-12-2017
PubMedCentral® Full Text Version
Post-print
Abstract
The regulation of microRNA (miRNA) biogenesis, function and degradation involves a range of mechanisms, including interactions with RNA-binding proteins. The potential contribution of regulatory miRNAs to the expression of these RNA interactor proteins that could control other miRNAs expression is still unclear. Here we demonstrate a regulatory circuit involving oncogenic and tumor-suppressor miRNAs and an RNA-binding protein in a chemotherapy-resistant ovarian cancer model. We identified and characterized miR-15a-5p and miR-25-3p as negative regulators of hnRNPA1 expression, which is required for the processing of miR-18a-3p, an inhibitor of the
Keywords
chemotherapy resistance, hnRNPA1, K-RAS, microRNAs, ovarian cancer, RNA-binding proteins
Published Open-Access
yes
Recommended Citation
Rodriguez-Aguayo, Cristian; Monroig, Paloma Del C; Redis, Roxana S; et al., "Regulation of hnRNPA1 by microRNAs Controls the miR-18a–K-RAS Axis in Chemotherapy-Resistant Ovarian Cancer" (2017). Faculty, Staff and Student Publications. 4281.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/4281
Correction
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Genetic Phenomena Commons, Medical Genetics Commons, Oncology Commons
Comments
This article has been corrected. See Cell Discov. 2023 Nov 8;9:111.