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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.)

Role of SOCS-1 Gene on Melanoma Cell Growth and Tumor Development

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Author(s):
Borin Scutti, Jorge A. [1] ; Matsuo, Alisson Leonardo [1] ; Pereira, Felipe Valenca [1] ; Massaoka, Mariana Hiromi [1] ; Figueiredo, Carlos Rogerio [1] ; Moreira, Dayson Friaca [2] ; Belizario, Jose Ernesto [2] ; Travassos, Luiz R. [1]
Total Authors: 8
Affiliation:
[1] Univ Fed Sao Paulo, Dept Microbiol Imunol & Parasitol, Unidade Oncol Expt, BR-04023062 Sao Paulo - Brazil
[2] Univ Sao Paulo, Dept Pharmacol, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: TRANSLATIONAL ONCOLOGY; v. 4, n. 2, p. 101-109, APR 2011.
Web of Science Citations: 17
Abstract

Melanoma is the most aggressive form of skin cancer, and its incidence has increased dramatically over the years. The murine B16F10 melanoma in syngeneic C57Bl/6 mice has been used as a highly aggressive model to investigate tumor development. Presently, we demonstrate in the B16F10-Nex2 subclone that silencing of SOCS-1, a negative regulator of Jak/Stat pathway, leads to reversal of the tumorigenic phenotype and inhibition of melanoma cell metastasis. SOCS-1 silencing with short hairpin RNA affected tumor growth and cell cycle regulation with arrest at the S phase with large-sized nuclei, reduced cell motility, and decreased melanoma cell invasion through Matrigel. A clonogenic assay showed that SOCS-1 acted as a modulator of resistance to anoikis. In addition, down-regulation of SOCS-1 decreased the expression of epidermal growth factor receptor ( mainly the phosphorylated-R), Ins-R alpha, and fibroblast growth factor receptor. In vivo, silencing of SOCS-1 inhibited subcutaneous tumor growth and metastatic development in the lungs. Because SOCS-1 is expressed in most melanoma cell lines and bears a relation with tumor invasion, thickness, and stage of disease, the present results on the effects of SOCS-1 silencing in melanoma suggest that this regulating protein can be a target of cancer therapy. (AU)

FAPESP's process: 06/50634-2 - Peptides and peptidases: biological activities in infectious diseases and cancer
Grantee:Luiz Rodolpho Raja Gabaglia Travassos
Support Opportunities: Research Projects - Thematic Grants