4.4 Article

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

期刊

CANCER BIOMARKERS
卷 34, 期 2, 页码 201-210

出版社

IOS PRESS
DOI: 10.3233/CBM-210353

关键词

Colorectal cancer; survival; microRNAs expression; microsatellite instability; prognostic biomarkers; stage III

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资金

  1. Fondo de Investigacion Sanitaria (FIS) Instituto de Salud Carlos III [Pi12/00172]
  2. Fundacion Mutua Madrilena
  3. Bayer Healthcare
  4. IMMUNOTHERCAN Comunidad de Madrid [S2017/BMD-3733]
  5. Fundacion 2000 Merck-Serono

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This study confirmed the association between miR-21 and miR-335 with microsatellite instability in colorectal cancer, and found a positive trend between miR-135a expression and RAS mutations. Furthermore, lower expression levels of miR-21 were associated with disease-free survival and overall survival, while high expression of miR-21 improved survival in poor prognosis patients.
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.

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