LINC00942通过与PTBP1相互作用提高PRKDC加速食管癌进展

IF 3.2 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhongqiu Wang, Kang Li, Xing Zhang, Feng Jiang, Lin Xu
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引用次数: 0

摘要

异常表达的LINC00942参与了几种癌症的进展。然而,LINC00942在食管癌(ESCA)中的功能尚不清楚。本研究旨在探讨LINC00942对ESCA的影响及其可能的分子机制。首先,使用GSE192662芯片分析ESCA中差异表达的lncrna。catRAPID omics v2.1用于预测可能与LINC00942相互作用的蛋白。利用SDS-PAGE银染色法、RNA拉下法和RIP法验证与LINC00942相互作用的蛋白。然后利用RNA seq检测PTBP1的下游靶点,利用KEGG富集分析分析参与增殖和迁移相关信号通路的基因。此外,采用CCK-8、EdU和transwell检测LINC00942对ESCA细胞功能的影响。生物信息学显示,LINC00942在ESCA中显著过表达。低表达LINC00942的患者预后明显较好。敲除LINC00942后,TE-1和OE19的增殖和迁移明显减少。随后,PTBP1被发现与LINC00942相互作用,PRKDC是PTBP1的下游靶点。功能分析显示,过表达LINC00942后,TE-1和OE19细胞的增殖和迁移明显增加,而敲低PRKDC可显著逆转这一作用。机制上,LINC00942通过与PTBP1相互作用促进PRKDC表达。综上所述,LINC00942通过与PTBP1结合促进PRKDC表达,促进ESCA细胞的增殖和迁移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

LINC00942 Accelerates Esophageal Cancer Progression by Raising PRKDC Through Interaction With PTBP1

LINC00942 Accelerates Esophageal Cancer Progression by Raising PRKDC Through Interaction With PTBP1

Aberrantly expressed LINC00942 is participated in the progression of several cancers. However, the function of LINC00942 in esophageal cancer (ESCA) is unclear. The objective of this study was to explore the effect of LINC00942 on ESCA and its possible molecular mechanisms. First, differentially expressed lncRNAs in ESCA were analyzed using GSE192662 microarray. catRAPID omics v2.1 was applied to predict the proteins that might interact with LINC00942. SDS-PAGE silver staining assay, RNA pull down, and RIP assay were utilized to validate proteins interacting with LINC00942. Then, RNA seq was applied to detect the downstream targets of PTBP1, and KEGG enrichment analysis was used to analyze the genes involved in proliferation and migration-related signaling pathways. In addition, CCK-8, EdU and transwell were used to detect the impact of LINC00942 on ESCA cell function. Bioinformatics revealed that LINC00942 was significantly overexpressed in ESCA. Patients in low-expression of LINC00942 had an obviously better prognosis. After LINC00942 knockdown, the proliferation and migration of TE-1 and OE19 were dramatically reduced. Subsequently, PTBP1 was found to interact with LINC00942, and PRKDC was a downstream target of PTBP1. Functional analysis showed that TE-1 and OE19 cell proliferation and migration were markedly elevated after LINC00942 overexpression, and knockdown of PRKDC significantly reversed this effect. Mechanistically, LINC00942 promoted PRKDC expression by interacting with PTBP1. In summary, LINC00942 facilitated the proliferation and migration of ESCA cells via binding to PTBP1 to promote PRKDC expression.

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来源期刊
CiteScore
5.80
自引率
2.80%
发文量
277
审稿时长
6-12 weeks
期刊介绍: The Journal of Biochemical and Molecular Toxicology is an international journal that contains original research papers, rapid communications, mini-reviews, and book reviews, all focusing on the molecular mechanisms of action and detoxication of exogenous and endogenous chemicals and toxic agents. The scope includes effects on the organism at all stages of development, on organ systems, tissues, and cells as well as on enzymes, receptors, hormones, and genes. The biochemical and molecular aspects of uptake, transport, storage, excretion, lactivation and detoxication of drugs, agricultural, industrial and environmental chemicals, natural products and food additives are all subjects suitable for publication. Of particular interest are aspects of molecular biology related to biochemical toxicology. These include studies of the expression of genes related to detoxication and activation enzymes, toxicants with modes of action involving effects on nucleic acids, gene expression and protein synthesis, and the toxicity of products derived from biotechnology.
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