| Literature DB >> 29434952 |
Hui Zhao1,2, Guosheng Wu3, Ji Zhu1, Mengyan Sun1, Yuchong Wang1, Yongjie Fan1, Kai Wu1, Hongda Bi1, Haiying Dai1, Chuan Lv1, Chunyu Xue1.
Abstract
Malignant melanoma is a class of highly malignant tumors derived from melanocytes. At present, the dysregulated gene expression involved in the progression of melanoma has attracted much attention. In the present study, the gene expression profile of human melanoma tissue was screened using a cDNA microarray, and it was identified that melanocyte-specific gene 1 (MSG1) was significantly overexpressed in melanoma tissue compared with paired nevus tissues. The overexpression of MSG1 in melanoma was subsequently confirmed using immunohistochemistry in a set of melanoma tissues. It was additionally identified that the overexpression of MSG1 may promote cell viability and inhibit cell apoptosis in human melanoma A375 cells, thus promoting melanoma progression. Mechanistically, following screening of the expression of apoptosis-associated proteins, MSG1 was demonstrated to enhance the expression of the apoptosis inhibitor B-cell lymphoma 2 (Bcl-2) to inhibit melanoma cell apoptosis. Therefore, it was concluded that the overexpression of MSG1 inhibits apoptosis by enhancing Bcl-2 expression in malignant melanoma, thus promoting melanoma progression.Entities:
Keywords: Bcl-2; apoptosis; cell viability; melanocyte-specific gene 1; melanoma
Year: 2017 PMID: 29434952 PMCID: PMC5777294 DOI: 10.3892/ol.2017.7592
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967