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Down-regulation of circPVRL3 promotes the proliferation and migration of gastric cancer cells

机译:Circpvrl3的下调促进了胃癌细胞的增殖和迁移

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Circular RNA (circRNA) is a key regulator in the development and progression of various types of carcinomas. However, its role in gastric cancer (GC) tumorigenesis is not well understood. The present study aimed to investigate the expression profile and potential modulation of circRNAs on GC carcinogenesis. Human circRNA microarray was performed to screen for abnormally expressed circRNA in GC tissue. Results showed that a decrease in the circPVRL3 expression level was associated with the presence of GC, and also with higher TNM stage and lower overall survival rates compared with that in adjacent noncancerous tissues. In vitro assays of the GC cell lines MKN-45 and MGC-803 demonstrated that knockdown of circPVRL3 promoted cell proliferation significantly. Prediction and annotation revealed circPVRL3 was able to sponge to 9 miRNAs and may be also able to have a binding with AGO2, FUS, LIN28A, PTB, and EIF4A3. In addition, based on the structure of internal ribosomal entry sites, open reading frame, and m6A modification, circPVRL3 may have the potential ability to encode proteins. Taken together, our study indicated that down-regulation of circPVRL3 could promote the proliferation in gastric carcinoma and have potential to encode protein.
机译:圆形RNA(CircRNA)是各种类型的癌症的开发和进展中的关键调节因子。然而,它在胃癌(GC)肿瘤发生中的作用尚不清楚。本研究旨在探讨GC致癌术中CircrNA的表达谱和潜在调节。进行人CircRNA微阵列对筛选GC组织中异常表达的CircrNA。结果表明,与邻近的非癌组织相比,CIVPVR1表达水平的降低与GC的存在相关,也具有较高的TNM阶段和较低的总存活率。 GC细胞系MKN-45和MKC-803的体外测定证明了CircPVR13的敲低显着促进了细胞增殖。预测和注释揭示了Circpvrl3能够将其海绵到9 miRNA,并且也可以与前一个结合2,Fus,Lin28a,ptb和Eif4a3。另外,基于内部核糖体进入位点的结构,开放阅读框架和M6A改性,CirPVR13可以具有编码蛋白质的潜在能力。我们的研究表明,CirPVRL3的下调可以促进胃癌中的增殖,并具有编码蛋白质的潜力。

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