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Detalle de: MicroRNAs as potential predictors of extreme response to tyrosine kinase inhibitors in renal cell cancer

Title MicroRNAs as potential predictors of extreme response to tyrosine kinase inhibitors in renal cell cancer
Abstract

Background MicroRNAs play an important role as modulators of gene expression in several biological processes and are closely related to development and cell differentiation regulation. Previous works have revealed a potential predictive role for miRNAs in different tumor types. This study aims to analyze the ability of miRNAs in segregating metastatic renal cell carcinoma patients according to their responses to tyrosine kinase inhibitors (TKIs). Methods Extreme responders were considered in the study and were defined as those patients that either had a long-term response (LR) (progression-free survival ˃11 months) or those that were primary refractory (PR) (progression as best response). The expression of 754 miRNAs was analyzed in tumor tissue of these 2 sets of patients. Results In a study cohort (n = 15) 4 miRNAs were significantly associated with patient response and differentially expressed in PR vs. LR (up-regulated in PR vs. LR: miR-425-5p, down-regulated in PR vs. LR: miR-139-3p, let-7d and let-7e). Further analysis in a validation cohort (n = 36) revealed similar results. Conclusion The present data strength the potential role of miRNAs as a tool to predict treatment outcomes in patients with metastatic renal cell carcinoma treated with TKIs.

Apa Reference Garrigós, C., Molina-Pinelo, S., Meléndez, R., Espinosa, M., Lerma, A., Taron, M., García-Donas, J., Rodriguez-Antona, C. & Duran, I. (2020). MicroRNAs as potential predictors of extreme response to tyrosine kinase inhibitors in renal cell cancer. Urologic Oncology: Seminars and Original Investigations, 38(7), 640.e23-640.e29. 10.1016/j.urolonc.2020.01.012
Doi 10.1016/j.urolonc.2020.01.012
Publication Date Jul 2020
Publication Type Article
Researcher Sonia Molina Pinelo
Ontology Transcriptomics, Expression Profiling, Regulatory biology, Drug Discovery and design, miRNA, Non-coding RNA
Research Groups
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