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Long noncoding RNA MEG3 regulates LATS2 by promoting the ubiquitination of EZH2 and inhibits proliferation and invasion in gallbladder cancer

机译:长非编码RNA MEG3通过促进EZH2的泛素化来调节LATS2并抑制胆囊癌的增殖和侵袭

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摘要

Gallbladder cancer (GBC) is the most common type of biliary tract cancer worldwide. Long noncoding RNAs (lncRNAs) play essential roles in physiological and pathological development. LncRNA MEG3, a tumor suppressor, has been reported to play important roles in some cancers, but the role of MEG3 in GBC remains largely unknown. The purpose of the present study was to explore the role of MEG3 in proliferation and invasion and the potential molecular mechanism in GBC. We found that MEG3 was downregulated in GBC tissues and cells, and low expression of MEG3 was correlated with poor prognostic outcomes in patients. Overexpression of MEG3 inhibited GBC cell proliferation and invasion, induced cell apoptosis and decreased tumorigenicity in nude mice. Moreover, we found that MEG3 was associated with EZH2 and attenuated EZH2 by promoting its ubiquitination. Furthermore, MEG3 executed its functions via EZH2 to regulate the downstream target gene LATS2. Taken together, these findings suggest that MEG3 is an effective target for GBC therapy and may facilitate the development of lncRNA-directed diagnostics and therapeutics against GBC.
机译:胆囊癌(GBC)是全世界最常见的胆道癌类型。长非编码RNA(lncRNA)在生理和病理学发展中起重要作用。据报道,LncRNA MEG3是一种肿瘤抑制因子,在某些癌症中起着重要的作用,但是在GBC中MEG3的作用仍然未知。本研究的目的是探讨MEG3在GBC中的增殖和侵袭作用以及潜在的分子机制。我们发现,MEG3在GBC组织和细胞中被下调,而MEG3的低表达与患者预后不良有关。 MEG3的过表达抑制了裸鼠的GBC细胞增殖和侵袭,诱导了细胞凋亡并降低了致瘤性。此外,我们发现MEG3与EZH2相关联,并通过促进其泛素化作用减弱了EZH2。此外,MEG3通过EZH2执行其功能,以调节下游靶基因LATS2。综上所述,这些发现表明MEG3是GBC治疗的有效靶标,并且可能促进针对GBC的lncRNA定向诊断和治疗方法的发展。

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