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首页> 外文期刊>Oncology letters >miR-186 suppressed CYLD expression and promoted cell proliferation in human melanoma
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miR-186 suppressed CYLD expression and promoted cell proliferation in human melanoma

机译:miR-186抑制人黑素瘤中CYLD的表达并促进细胞增殖

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摘要

Previous studies have shown that microRNA-186 (miR-186) is overexpressed in various human cancers and is associated with the regulation of the carcinogenic processes. However, the underlying mechanisms of this microRNA in melanoma remain largely unknown. In the present study, the overexpression of miR-186 was identified in melanoma tissues and melanoma cells compared to the expression of miR-186 in the matched tumor adjacent tissues and normal human epidermal melanocytes. Overexpression of miR-186 promoted the proliferation and anchorage-independent growth of melanoma cells, whereas inhibition of miR-186 reduced this effect. Bioinformatics analysis also revealed cylindromatosis (CYLD), a putative tumor suppressor, to be a potential target of miR-186. Luciferase reporter assays showed that miR-186 directly targeted the 3-untranslated regions of CYLD messenger RNA. Additional experiments showed that overexpression of miR-186 promoted the proliferation of melanoma cells, which was consistent with the inhibitory effects induced by knockdown of CYLD. In summary, the present study indicated that miRNA-186 plays a crucial role in melanoma growth and its oncogenic effect is mediated chiefly through the direct suppression of CYLD expression.
机译:先前的研究表明,microRNA-186(miR-186)在各种人类癌症中均过表达,并且与致癌过程的调控有关。但是,这种黑色素瘤在黑色素瘤中的潜在机制仍然未知。在本研究中,与匹配的肿瘤邻近组织和正常人表皮黑素细胞中miR-186的表达相比,在黑素瘤组织和黑素瘤细胞中发现了miR-186的过表达。 miR-186的过表达促进了黑色素瘤细胞的增殖和锚定非依赖性生长,而对miR-186的抑制则降低了这种作用。生物信息学分析还表明,推定的肿瘤抑制因子圆柱状增生(CYLD)是miR-186的潜在靶标。萤光素酶报告基因检测表明,miR-186直接靶向CYLD信使RNA的3个非翻译区。额外的实验表明,miR-186的过表达促进黑色素瘤细胞的增殖,这与CYLD敲低诱导的抑制作用一致。总之,本研究表明miRNA-186在黑色素瘤生长中起关键作用,其致癌作用主要通过直接抑制CYLD表达来介导。

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