miR-542-3p/PIK3R1轴参与hsa_circ_0087104介导的食管鳞状细胞癌转移抑制。

IF 3.6 3区 医学 Q2 ONCOLOGY
American journal of cancer research Pub Date : 2024-12-15 eCollection Date: 2024-01-01 DOI:10.62347/EFEO7205
Shan Gao, Weiyang Lou
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引用次数: 0

摘要

食管鳞状细胞癌(ESCC)是食管癌中最主要的亚型,以其高淋巴结转移潜力和预后差而臭名昭著。越来越多的证据证明了环状rna在人类恶性肿瘤中的关键功能。然而,对环状rna在ESCC淋巴结转移中的作用的认识仍然不足。在本研究中,进行了一系列的生物信息学分析和实验验证。通过对GEO数据集GSE150476进行差异表达分析和筛选,共鉴定出8个与ESCC淋巴结转移相关的环状rna。表达分析证实了它们在ESCC组织(相对于正常组织)或转移部位(相对于原发部位)的低表达。通过结合来自CSCD和starBase数据库的结合mirna,预测了6个潜在mirna (miR-532-5p、miR-2681-5p、miR-670-5p、miR-1252-5p、miR-382-3p和miR-542-3p),并构建了circRNA-miRNA调控网络。接下来,预测695个靶基因与6个mirna结合。通过蛋白-蛋白相互作用(PPI)网络分析、枢纽基因鉴定和表达分析,我们发现枢纽基因PIK3R1是ESCC中hsa_circ_0087104/miR-542-3p最潜在的下游靶基因。与正常食管上皮细胞系相比,ESCC细胞中Hsa_circ_0087104和PIK3R1表达降低,miR-542-3p表达升高。荧光素酶报告基因和MS2-RIP实验证实了miR-542-3p与hsa_circ_0087104或PIK3R1的直接结合。Hsa_circ_0087104增加了PIK3R1的表达,但miR-542-3p的异位表达逆转了Hsa_circ_0087104介导的ESCC中PIK3R1过表达。过表达hsa_circ_0087104可抑制ESCC细胞的体外迁移和侵袭,上调miR-542-3p可减弱这种抑制作用。总的来说,目前的研究结果阐明了hsa_circ_0087104/miR-542-3p/PIK3R1轴可能参与抑制ESCC的淋巴结转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
miR-542-3p/PIK3R1 axis is involved in hsa_circ_0087104-mediated inhibition of esophageal squamous cell carcinoma metastasis.

Esophageal squamous cell carcinoma (ESCC), the most predominant subtype of esophageal cancer, is notorious for its high lymph node metastatic potential and poor prognosis. Growing evidence has demonstrated crucial function of circRNAs in human malignancies. However, the knowledge of circRNAs in lymph node metastasis of ESCC is still inadequate. In this study, a series of bioinformatic analyses and experimental validation were performed. By performing differential expression analysis and selection for GEO dataset GSE150476, a total of 8 circRNAs associated with lymph node metastasis of ESCC were identified. Expression analysis confirmed their low expression in ESCC tissues (relative to normal tissues) or metastatic sites (relative to primary sites). By combination of binding miRNAs from CSCD and starBase databases, six potential miRNAs (miR-532-5p, miR-2681-5p, miR-670-5p, miR-1252-5p, miR-382-3p and miR-542-3p) were predicted and a circRNA-miRNA regulatory network was constructed. Next, 695 target genes were predicted to bind to the 6 miRNAs. After conducting protein-protein interaction (PPI) network analysis, hub gene identification and expression analysis, a hub gene PIK3R1 was identified as the most potential downstream target gene of hsa_circ_0087104/miR-542-3p in ESCC. Hsa_circ_0087104 and PIK3R1 were decreased while miR-542-3p was increased in ESCC cells compared with normal esophageal epithelial cell line. Luciferase reporter and MS2-RIP assays confirmed the direct bind of miR-542-3p to hsa_circ_0087104 or PIK3R1. Hsa_circ_0087104 increased PIK3R1 expression but ectopic expression of miR-542-3p reversed hsa_circ_0087104-mediated PIK3R1 overexpression in ESCC. Overexpression of hsa_circ_0087104 suppressed in vitro migration and invasion of ESCC cells and this suppressive effect could be weakened by upregulation of miR-542-3p. Collectively, the current findings elucidated a potential hsa_circ_0087104/miR-542-3p/PIK3R1 axis that might be involved in suppression of lymph node metastasis of ESCC.

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来源期刊
自引率
3.80%
发文量
263
期刊介绍: The American Journal of Cancer Research (AJCR) (ISSN 2156-6976), is an independent open access, online only journal to facilitate rapid dissemination of novel discoveries in basic science and treatment of cancer. It was founded by a group of scientists for cancer research and clinical academic oncologists from around the world, who are devoted to the promotion and advancement of our understanding of the cancer and its treatment. The scope of AJCR is intended to encompass that of multi-disciplinary researchers from any scientific discipline where the primary focus of the research is to increase and integrate knowledge about etiology and molecular mechanisms of carcinogenesis with the ultimate aim of advancing the cure and prevention of this increasingly devastating disease. To achieve these aims AJCR will publish review articles, original articles and new techniques in cancer research and therapy. It will also publish hypothesis, case reports and letter to the editor. Unlike most other open access online journals, AJCR will keep most of the traditional features of paper print that we are all familiar with, such as continuous volume, issue numbers, as well as continuous page numbers to retain our comfortable familiarity towards an academic journal.
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