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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

MiR-223-5p works as an oncomiR in vulvar carcinoma by TP63 suppression

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Author(s):
Maia, Beatriz de Melo ; Rodrigues, Iara Santana ; Akagi, Erica Mie ; do Amaral, Nayra Soares ; Ling, Hui ; Monroig, Paloma ; Soares, Fernando Augusto ; Calin, George Adrian ; Rocha, Rafael Malagoli
Total Authors: 9
Document type: Journal article
Source: ONCOTARGET; v. 7, n. 31, p. 49217-49231, AUG 2 2016.
Web of Science Citations: 9
Abstract

MiR-223-5p has been previously mentioned to be associated with tumor metastasis in HPV negative vulvar carcinomas, such as in several other tumor types. In the present study, we hypothesized that this microRNA would be important in vulvar cancer carcinogenesis and progression. To investigate this, we artificially mimicked miR-223-5p expression in a cell line derived from lymph node metastasis of vulvar carcinoma (SW962) and performed in vitro assays. As results, lower cell proliferation (p < 0.01) and migration (p < 0.001) were observed when miR-223-5p was overexpressed. In contrast, increased invasive potential of these cells was verified (p < 0.004). In silico search indicated that miR-223-5p targets TP63, member of the TP53 family of proteins, largely described with importance in vulvar cancer. We experimentally demonstrated that this microRNA is capable to decrease levels of p63 at both mRNA and protein levels (p < 0.001, and p < 0.0001; respectively). Also, a significant inverse correlation was observed between miR-223-5p and p63 expressions in tumors from patients (p = 0.0365). Furthermore, low p63 protein expression was correlated with deeper tumor invasion (p = 0.0491) and lower patient overall survival (p = 0.0494). Our study points out miR-223-5p overexpression as a putative pathological mechanism of tumor invasion and a promising therapeutic target and highlights the importance of both miR-223-5p and p63 as prognostic factors in vulvar cancer. Also, it is plausible that the evaluation of p63 expression in vulvar cancer at the biopsy level may bring important contribution on prognostic establishment and in elaborating better surgical approaches for vulvar cancer patients. (AU)

FAPESP's process: 13/04075-5 - Design and transfection of microRNAs as a therapeutical strategy in vulvar carcinomas
Grantee:Beatriz de Melo Maia
Support Opportunities: Scholarships abroad - Research Internship - Doctorate
FAPESP's process: 11/18065-6 - Evaluation of the role of microRNA in vulvar carcinoma
Grantee:Beatriz de Melo Maia
Support Opportunities: Scholarships in Brazil - Doctorate