{"title":"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","authors":"Zhengjia Liu, Xiyu Liu, Cong Yin, Zihao Liu, Haixiang Yu","doi":"10.1007/s12013-025-01753-y","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":510,"journal":{"name":"Cell Biochemistry and Biophysics","volume":" ","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification of circRNA-Based Biomarkers and ceRNA Mechanism in Non-Small Cell Lung Cancer.\",\"authors\":\"Zhengjia Liu, Xiyu Liu, Cong Yin, Zihao Liu, Haixiang Yu\",\"doi\":\"10.1007/s12013-025-01753-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":510,\"journal\":{\"name\":\"Cell Biochemistry and Biophysics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-04-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell Biochemistry and Biophysics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s12013-025-01753-y\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Biochemistry and Biophysics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12013-025-01753-y","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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.
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.