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Association of miR-21 and miR-335 to microsatellite instability and prognosis in stage III colorectal cancer.

Authors :
Calvo-López, Tania
Paz-Cabezas, Mateo
Llovet, Patricia
Ibañez, Maria Dolores
Sastre, Javier
Alonso-Orduña, Vicente
Viéitez, J.Ma.
Yubero, Alfonso
Vera, Ruth
Asensio-Martínez, Elena
Garcia-Alfonso, Pilar
Aranda, Enrique
Diaz-Rubio, Eduardo
Perez-Villamil, Beatriz
Source :
Cancer Biomarkers. 2022, Vol. 34 Issue 2, p201-210. 10p.
Publication Year :
2022

Abstract

BACKGROUND: MicroRNAs (miRs) are frequently altered in colorectal cancer (CRC) and can be used as prognostic factors. OBJECTIVE: To confirm in stage III CRC patients a reported miR signature that was associated to the presence of metastatic disease. To correlate miR expression with microsatellite instability (MSI) and mutations in RAS and BRAF. METHODS: miR-21, miR-135a, miR-206, miR-335 and miR-Let-7a expression was analyzed by RT-qPCR in 150 patients out of the 329 patients used to analyze MSI and RAS and BRAF mutations. Association with disease free survival (DFS) and overall survival (OS) was analyzed. Data was confirmed by a multivariate analysis. RESULTS: MiR-21 high expression (p = 0.034) and miR-335 low expression (p = 0.0061) were significantly associated with MSI-H. A positive trend (p = 0.0624) between miR-135a high expression and RAS mutations was found. Lower miR-21 expression levels are associated with DFS (HR = 2.654, 95% CI: 1.066–6.605, p = 0.036) and a trend with OS (HR = 2.419, 95% CI: 0.749–7.815, p = 0.140). MiR-21 high expression significantly improves DFS of the poor prognosis group (T4 or N2) (p = 0.03). CONCLUSIONS: Association of increased expression of miR-21 and better prognosis in the poor prognostic group may be of interest and could be explored in future prospective clinical trials. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15740153
Volume :
34
Issue :
2
Database :
Academic Search Index
Journal :
Cancer Biomarkers
Publication Type :
Academic Journal
Accession number :
157146150
Full Text :
https://doi.org/10.3233/CBM-210353