环状rna生物标志物的鉴定及其在非小细胞肺癌中的作用机制

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhengjia Liu, Xiyu Liu, Cong Yin, Zihao Liu, Haixiang Yu
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引用次数: 0

摘要

我们旨在鉴定circRNA作为非小细胞肺癌(NSCLC)的生物标志物,并探索其潜在机制。circRNA和mRNA数据从GEO数据库检索。采用差异表达分析、加权基因共表达网络分析(WGCNA)、随机森林和支持向量机算法等一系列生物信息学分析方法鉴定NSCLC中的关键环状rna。ROC曲线用于评估和区分关键环状rna在癌症中的作用。通过qPCR分析验证circrna的表达水平。最后,构建了ceRNA网络。本研究将si-hsa_circ_0084443转染到NSCLC细胞中,研究其在NSCLC中的功能。5种circrna (hsa_circ_0049271、hsa_circ_0029426、hsa_circ_0084443、hsa_circ_0015278和hsa_circ_0024731)被鉴定为NSCLC的生物标志物。它们在识别非小细胞肺癌方面表现出强大的诊断能力,AUC为0.85。qPCR结果显示,与正常组织相比,hsa_circ_0049271、hsa_circ_0029426和hsa_circ_0015278在肿瘤组织中显著下调,hsa_circ_0084443和hsa_circ_0024731在肿瘤组织中显著上调(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of circRNA-Based Biomarkers and ceRNA Mechanism in Non-Small Cell Lung Cancer.

We aimed to identify circRNA as a biomarker in non-small cell lung cancer (NSCLC) and explore the underlying mechanism. circRNA and mRNA data were retrieved from GEO database. A series of bioinformatics analyses including differentially expressed analysis, weighted gene co-expression network analysis (WGCNA), Random Forest, and support vector machine algorithm were applied to identify the key circRNAs in NSCLC. ROC curves were used to evaluate and distinguish the roles of key circRNAs in cancer. The expression levels of circRNAs were validated via qPCR analysis. Finally, a ceRNA network was constructed. Herein, si-hsa_circ_0084443 was transfected into NSCLC cells to investigate its function in NSCLC. Five circRNAs (hsa_circ_0049271, hsa_circ_0029426, hsa_circ_0084443, hsa_circ_0015278, and hsa_circ_0024731) were identified as biomarkers in NSCLC. They exhibited potent diagnostic ability in identifying NSCLC, with AUC > 0.85. qPCR results suggested that hsa_circ_0049271, hsa_circ_0029426, and hsa_circ_0015278 were significantly downregulated and hsa_circ_0084443 and hsa_circ_0024731 were significantly upregulated in tumor tissue compared with the levels in normal tissues (P < 0.05). A ceRNA network was finally constructed. Knockdown of hsa_circ_0084443 inhibited cell growth, migration, invasion, and colony formation, and promoted apoptosis in NSCLC cell line. Five circRNAs were identified as biomarkers and demonstrated abnormal expression in NSCLC. Furthermore, ceRNA network was constructed, which can aid the mechanism exploration in the future.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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