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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.)

microRNA Portraits in Human Vulvar Carcinoma

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Author(s):
Maia, Beatriz de Melo [1] ; Lavorato-Rocha, Andre Mourao [1] ; Rodrigues, Lara Sant'Ana [1] ; Coutinho-Camillo, Claudia Malheiros [1] ; Baiocchi, Glauco [2] ; Stiepcich, Monica Maria [3] ; Puga, Renato [4] ; Lima, Leandro de A. [5] ; Soares, Fernando Augusto [1] ; Rocha, Rafael Malagoli [1]
Total Authors: 10
Affiliation:
[1] Univ Sao Paulo, Hosp AC Camargo, Dept Anat Pathol, Sao Paulo - Brazil
[2] Univ Sao Paulo, Hosp AC Camargo, Dept Gynecol Oncol, Sao Paulo - Brazil
[3] Univ Sao Paulo, Dept Pathol, Fleury Inst, Sao Paulo - Brazil
[4] Univ Sao Paulo, Fac Med, Dept Psychiat, Sao Paulo - Brazil
[5] CIPE Hosp AC Camargo, Lab Bioinformat & Biostat, Sao Paulo - Brazil
Total Affiliations: 5
Document type: Journal article
Source: Cancer Prevention Research; v. 6, n. 11, p. 1231-1241, NOV 2013.
Web of Science Citations: 10
Abstract

Unregulated expression of microRNAs is well known and has already been demonstrated in many tumor types. However, in vulvar carcinoma this field has been unknown territory. Our study characterizes microRNA in vulvar tumors through an expression profile of 754 miRNAs, relating this with clinical and anatomopathologic data, and presence of HPV infection. Twenty HPV-negative and 20 HPV-positive samples, genotyped for high-risk HPVs (HPV16, 18, 31, 33) and a pool of seven normal vulvar skin samples were used for the identification of differentially expressed miRNAs by TLDA Quantitative Real Time PCR (qRT-PCR). Twenty-five differentially expressed microRNAs between HPV-positive and HPV-negative groups and 79 differentially expressed on the tumor compared with normal samples were obtained. A network between microRNA expression profiles and putative target mRNAs predicted by target prediction algorithms and previously demonstrated as relevant in vulvar carcinomas, such as TP53, RB, PTEN, and EGFR was constructed. Downregulation of both miR-223-5p and miR-19-b1-5p were correlated with the presence of lymph node metastasis; downregulation of miR-100-3p and miR-19-b1-5p were correlated with presence of vascular invasion; overexpression of miR-519b and miR-133a were associated with advanced FIGO staging. In conclusion, our study demonstrates that microRNAs may be clinically important in vulvar carcinomas and our findings may help for further studies on functional implications of miRNA deregulation in this type of cancer. (AU)

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