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MicroRNA-7-5p′s role in the O-GlcNAcylation and cancer metabolism

机译:microRNA-7-5P在O-Glcnacylation和癌症新陈代谢中的作用

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摘要

O-GlcNAc Transferase (OGT) is a complementary enzyme that regulates O-linked N-acetylglucosaminylation(O-GlcNAcylation) and plays a critical role in various cancer phenotypes, including invasion, migration, and metabolic reprogramming. In our previous study we found that miR-7-5p was downregulated at lung cancer cells with highly metastatic capacity. In the in-silico approach, OGT is the predicted target of miR-7-5p. To identify miR-7-5p′s role in cell growth and metabolism, we transfected various lung cancer cell lines with miR-7-5p. The expression level of miR-7-5p was confirmed by qRT-PCR in lung cancer cell lines. Western blot assays and qRT-PCR were performed to demonstrate miR-7-5p′s effect. Bioinformatic analysis indicated that OGT is a direct target of miR-7-5p. The binding sites of miR-7-5p in the OGT 3′ UTR were verified by luciferase reporter assay. To investigate the role of miR-7-5p in the cancer metabolism of non-small cell lung cancer (NSCLC) cells, mimic of miR-7-5p was transfected into NSCLC cells, and the effect of miR-7-5p on cancer metabolism was analyzed by LDH assays, glucose uptake, and mitochondrial ATP synthase inhibitor assay. O-GlcNAcylated protein level was determined by Western blot. The role of miR-7-5p in lung cancer growth was measured by MTS assays. To identify the delivery of miR-7-5p via PLGA, an in vitro release assay of PLGA-miR-7-5p was done. miR-7-5p was highly expressed whereas OGT showed low expression in H358, H827. However, miR-7-5p exhibited low expression while OGT had high expression in H522, H460, and H1299 cell lines. OGT were repressed by binding of miR-7a-5p to the 3′-UTR. Overexpression of miR-7-5p also diminished anaerobic glycolysis. miR-181a-5p transfection induced expression levels of OGT were diminished compared to those in the control group. O-GlcNAcylation was suppressed by miR-7-5p. Moreover, the overexpression of miR-7-5a suppressed lung cancer cell growth. miR-7-5p was released via PLGA for up to 10 days. In the present study, inhibition of OGT by miR-7-5p decreased the growth and cancer metabolism of lung cancer.
机译:O-GlcNAc转移酶(OGT)是一种互补酶,其调节O-连接的N-乙酰葡糖胺蛋白酶(O-Glcnacylation),并在各种癌症表型中起重要作用,包括侵袭,迁移和代谢重编程。在我们以前的研究中,我们发现MiR-7-5P以高度转移的能力下调肺癌细胞。在In-Silico方法中,OGT是MIR-7-5P的预测目标。为了鉴定miR-7-5p在细胞生长和新陈代谢中的作用,我们用miR-7-5p转染各种肺癌细胞系。通过肺癌细胞系QRT-PCR确认miR-7-5p的表达水平。进行蛋白质印迹测定和QRT-PCR以证明miR-7-5p的效果。生物信息分析表明OGT是MIR-7-5P的直接靶标。通过Luciferase报告器测定验证OGT 3'UTR中miR-7-5p的结合位点。为了探讨MIR-7-5P在非小细胞肺癌(NSCLC)细胞的癌症代谢中的作用,将MIR-7-5P的模拟转染到NMSCLC细胞中,以及MIR-7-5P对癌症的影响通过LDH测定,葡萄糖摄取和线粒体ATP合酶抑制剂测定分析代谢。通过Western印迹测定O-甘氨酸蛋白水平。 MIR-7-5P在肺癌生长中的作用是通过MTS测定法测定的。为了通过PLGA鉴定miR-7-5p的递送,完成了PLGA-miR-7-5p的体外释放测定。 MiR-7-5P高表达,而OGT在H358,H827中显示出低表达。然而,MIR-7-5P表现出低表达,而OGT在H522,H460和H1299细胞系中具有高表达。通过将miR-7a-5p与3'-UTR结合来压抑OGT。 miR-7-5p的过度表达还减少了厌氧糖醇分解。与对照组中的那些相比,MiR-181A-5P转染诱导的OGT的表达水平降低。 MiR-7-5P抑制了o-glcnacylation。此外,miR-7-5a的过表达抑制了肺癌细胞生长。 MiR-7-5P通过PLGA释放最多10天。在本研究中,MIR-7-5P对OGT的抑制降低了肺癌的生长和癌症代谢。

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