Zhao Hui, Wu Guosheng, Zhu Ji, Sun Mengyan, Wang Yuchong, Fan Yongjie, Wu Kai, Bi Hongda, Dai Haiying, Lv Chuan, Xue Chunyu
Department of Plastic Surgery, Changhai Hospital, Shanghai 200433, P.R. China.
Department of Plastic Surgery, The Second Sanatorium of Jinan Military Region, Qingdao, Shandong 266000, P.R. China.
Oncol Lett. 2018 Feb;15(2):2413-2418. doi: 10.3892/ol.2017.7592. Epub 2017 Dec 12.
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 () was significantly overexpressed in melanoma tissue compared with paired nevus tissues. The overexpression of in melanoma was subsequently confirmed using immunohistochemistry in a set of melanoma tissues. It was additionally identified that the overexpression of 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, 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 inhibits apoptosis by enhancing Bcl-2 expression in malignant melanoma, thus promoting melanoma progression.
恶性黑色素瘤是一类源自黑素细胞的高度恶性肿瘤。目前,黑色素瘤进展过程中涉及的基因表达失调备受关注。在本研究中,使用cDNA微阵列筛选了人黑色素瘤组织的基因表达谱,并且鉴定出黑素细胞特异性基因1()在黑色素瘤组织中与配对的痣组织相比显著过表达。随后在一组黑色素瘤组织中使用免疫组织化学证实了黑色素瘤中该基因的过表达。另外还鉴定出该基因的过表达可能促进人黑色素瘤A375细胞的细胞活力并抑制细胞凋亡,从而促进黑色素瘤进展。机制上,在筛选凋亡相关蛋白的表达后,证明该基因增强凋亡抑制因子B细胞淋巴瘤2(Bcl-2)的表达以抑制黑色素瘤细胞凋亡。因此,得出结论,该基因的过表达通过增强恶性黑色素瘤中Bcl-2的表达来抑制凋亡,从而促进黑色素瘤进展。