黑色素瘤
癌症研究
长非编码RNA
车站3
生物
微阵列
肿瘤进展
癌症
核糖核酸
信号转导
基因
基因表达
细胞生物学
遗传学
作者
Jingjing Ma,Qiong Shi,Sen Guo,Peng Xu,Xiuli Yi,Yuqi Yang,Weigang Zhang,Yu Liu,Lin Liu,Yue Qiao,Tao Zhao,Tianwen Gao,Weinan Guo,Chunying Li
标识
DOI:10.3389/fonc.2021.818178
摘要
Melanoma is the most lethal skin cancer that originates from epidermal melanocytes. Recently, long non-coding RNAs (lncRNAs) are emerging as critical regulators of cancer pathogenesis and potential therapeutic targets. However, the expression profile of lncRNAs and their role in melanoma progression have not been thoroughly investigated. Herein, we firstly obtained the expression profile of lncRNAs in primary melanomas using microarray analysis and unveiled the differentially-expressed lncRNAs compared with nevus. Subsequently, a series of bioinformatics analysis showed the great involvement of dysregulated lncRNAs in melanoma biology and immune response. Further, we identified lncRNA CD27-AS1-208 as a novel nuclear-localized factor with prominent facilitative role in melanoma cell proliferation, invasion and migration. Mechanistically, CD27-AS1-208 could directly interact with STAT3 and contribute to melanoma progression in a STAT3-dependent manner. Ultimately, the role of CD27-AS1-208 in melanoma progression
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