miR-155 and miR-484 Are Associated with Time to Progression in Metastatic Renal Cell Carcinoma Treated with Sunitinib.

Biomed Res Int

Central European Institute of Technology, Masaryk University, 625 00 Brno, Czech Republic ; Department of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, 656 53 Brno, Czech Republic.

Published: March 2016

AI Article Synopsis

  • Sunitinib, a tyrosine kinase inhibitor, is used to treat metastatic renal cell carcinoma, but patients often develop drug resistance and experience disease progression.
  • A study on tumor tissues from 79 patients identified specific miRNAs, with decreased levels of miR-155 and miR-484 linked to longer time to progression, suggesting their roles in resistance to sunitinib.
  • Understanding these miRNAs could lead to personalized treatment approaches for patients, improving therapy outcomes for metastatic renal cell carcinoma.

Article Abstract

Background. Sunitinib is a tyrosine kinase inhibitor used in the treatment of metastatic renal cell carcinoma. The main difficulty related to the treatment is the development of drug resistance followed by rapid progression of the disease. We analyzed tumor tissue of sunitinib treated patients in order to find miRNAs associated with therapeutic response. Methods. A total of 79 patients with metastatic renal cell carcinoma were included in our study. miRNA profiling in tumor tissue samples was performed by TaqMan Low Density Arrays and a group of selected miRNAs (miR-155, miR-374-5p, miR-324-3p, miR-484, miR-302c, and miR-888) was further validated by qRT-PCR. Normalized data were subjected to ROC and Kaplan-Meier analysis. Results. We reported decreased tissue levels of miR-155 and miR-484 as significantly associated with increased time to progression (miR-155: median TTP 5.8 versus 12.8 months, miR-484: median TTP 5.8 versus 8.9 months). Conclusion. miR-155 and miR-484 are potentially connected with sunitinib resistance and failure of the therapy. miR-155 is a known oncogene with direct influence on neovascularization. Biological role of miR-484 has to be clarified. Stratification of patients based on miRNA analysis would allow more personalized approach in therapy of metastatic renal cell carcinoma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433647PMC
http://dx.doi.org/10.1155/2015/941980DOI Listing

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