{"title":"机器学习和WGCNA揭示PVT1/ miR-143-3p /CDK1 ceRNA轴是NSCLC的关键调节因子","authors":"Arash Safarzadeh, Setareh Ataei, Arezou Sayad, Soudeh Ghafouri-Fard","doi":"10.1016/j.bbrep.2025.102292","DOIUrl":null,"url":null,"abstract":"<div><div>Machine learning has provided novel tools for analysis of multi-omics data for subgroups recognition in cancer to reach a clinically meaningful classification of cancer and identification of potential biomarkers. In this work, we retrieved mRNA, lncRNA, miRNA and protein expression data of non-small cell lung cancer (NSCLC) samples and used different machine learning methods for biomarker selection, diagnostic validation, construction of competing endogenous RNA network, identification of the hub axes and drug prediction. Integration of multi-omics data and machine learning resulted in identification of CDK1, TOP2A, AURKA, TPX2, BUB1B, and CENPF as key biomarkers in NSCLC. We also identified the PVT1/miR-143–3p/CDK1 axis and its associated transcription factors (FOXC1, YY1, and GATA2) as a potential regulatory network for additional investigations. These findings increase the understanding of NSCLC molecular processes and provide a foundation for developing targeted therapies and diagnostic tools.</div></div>","PeriodicalId":8771,"journal":{"name":"Biochemistry and Biophysics Reports","volume":"44 ","pages":"Article 102292"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Machine learning and WGCNA reveal the PVT1/miR-143–3p/CDK1 ceRNA axis as a key regulator in NSCLC\",\"authors\":\"Arash Safarzadeh, Setareh Ataei, Arezou Sayad, Soudeh Ghafouri-Fard\",\"doi\":\"10.1016/j.bbrep.2025.102292\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Machine learning has provided novel tools for analysis of multi-omics data for subgroups recognition in cancer to reach a clinically meaningful classification of cancer and identification of potential biomarkers. In this work, we retrieved mRNA, lncRNA, miRNA and protein expression data of non-small cell lung cancer (NSCLC) samples and used different machine learning methods for biomarker selection, diagnostic validation, construction of competing endogenous RNA network, identification of the hub axes and drug prediction. Integration of multi-omics data and machine learning resulted in identification of CDK1, TOP2A, AURKA, TPX2, BUB1B, and CENPF as key biomarkers in NSCLC. We also identified the PVT1/miR-143–3p/CDK1 axis and its associated transcription factors (FOXC1, YY1, and GATA2) as a potential regulatory network for additional investigations. These findings increase the understanding of NSCLC molecular processes and provide a foundation for developing targeted therapies and diagnostic tools.</div></div>\",\"PeriodicalId\":8771,\"journal\":{\"name\":\"Biochemistry and Biophysics Reports\",\"volume\":\"44 \",\"pages\":\"Article 102292\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemistry and Biophysics Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2405580825003796\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemistry and Biophysics Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405580825003796","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Machine learning and WGCNA reveal the PVT1/miR-143–3p/CDK1 ceRNA axis as a key regulator in NSCLC
Machine learning has provided novel tools for analysis of multi-omics data for subgroups recognition in cancer to reach a clinically meaningful classification of cancer and identification of potential biomarkers. In this work, we retrieved mRNA, lncRNA, miRNA and protein expression data of non-small cell lung cancer (NSCLC) samples and used different machine learning methods for biomarker selection, diagnostic validation, construction of competing endogenous RNA network, identification of the hub axes and drug prediction. Integration of multi-omics data and machine learning resulted in identification of CDK1, TOP2A, AURKA, TPX2, BUB1B, and CENPF as key biomarkers in NSCLC. We also identified the PVT1/miR-143–3p/CDK1 axis and its associated transcription factors (FOXC1, YY1, and GATA2) as a potential regulatory network for additional investigations. These findings increase the understanding of NSCLC molecular processes and provide a foundation for developing targeted therapies and diagnostic tools.
期刊介绍:
Open access, online only, peer-reviewed international journal in the Life Sciences, established in 2014 Biochemistry and Biophysics Reports (BB Reports) publishes original research in all aspects of Biochemistry, Biophysics and related areas like Molecular and Cell Biology. BB Reports welcomes solid though more preliminary, descriptive and small scale results if they have the potential to stimulate and/or contribute to future research, leading to new insights or hypothesis. Primary criteria for acceptance is that the work is original, scientifically and technically sound and provides valuable knowledge to life sciences research. We strongly believe all results deserve to be published and documented for the advancement of science. BB Reports specifically appreciates receiving reports on: Negative results, Replication studies, Reanalysis of previous datasets.