» Articles » PMID: 38696317

Identifying LncRNAs and MRNAs Related to Survival of NSCLC Based on Bioinformatic Analysis and Machine Learning

Overview
Specialty Geriatrics
Date 2024 May 2
PMID 38696317
Authors
Affiliations
Soon will be listed here.
Abstract

Non-small cell lung cancer (NSCLC) is the most common histopathological type, and it is purposeful for screening potential prognostic biomarkers for NSCLC. This study aims to identify the lncRNAs and mRNAs related to survival of non-small cell lung cancer (NSCLC). The expression profile data of lung adenocarcinoma and lung squamous cell carcinoma were downloaded in The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) dataset. A total of eight survival related long non-coding RNAs (lncRNAs) and 262 survival related mRNAs were filtered. By gene set enrichment analysis, 17 significantly correlated Gene Ontology signal pathways and 14 Kyoto Encyclopedia of Genes and Genomes signal pathways were screened. Based on the clinical survival and prognosis information of the samples, we screened eight lncRNAs and 193 mRNAs by single factor Cox regression analysis. Further single and multifactor Cox regression analysis were performed, 30 independent prognostication-related mRNAs were obtained. The PPI network was further constructed. We then performed the machine learning algorithms (Least absolute shrinkage and selection operator, Recursive feature elimination, and Random forest) to screen the optimized DEGs combination, and a total of 17 overlapping mRNAs were obtained. Based on the 17 characteristic mRNAs obtained, we firstly built a Nomogram prediction model, and the ROC values of training set and testing set were 0.835 and 0.767, respectively. By overlapping the 17 characteristic mRNAs and PPI network hub genes, three genes were obtained: CDC6, CEP55, TYMS, which were considered as key factors associated with survival of NSCLC. The experiments were performed to examine the effect of CDC6, CEP55, and TYMS on NSCLC cells. Finally, the lncRNAs-mRNAs networks were constructed.

Citing Articles

Artificial intelligence in lung cancer: current applications, future perspectives, and challenges.

Huang D, Li Z, Jiang T, Yang C, Li N Front Oncol. 2025; 14:1486310.

PMID: 39763611 PMC: 11700796. DOI: 10.3389/fonc.2024.1486310.

References
1.
Brody H . Lung cancer. Nature. 2020; 587(7834):S7. DOI: 10.1038/d41586-020-03152-0. View

2.
Cheng J, Pan Y, Huang W, Huang K, Cui Y, Hong W . Differentiation between immune checkpoint inhibitor-related and radiation pneumonitis in lung cancer by CT radiomics and machine learning. Med Phys. 2022; 49(3):1547-1558. PMC: 9306809. DOI: 10.1002/mp.15451. View

3.
Tsyganov M, Rodionov E, Ibragimova M, Miller S, Cheremisina O, Frolova I . Personalized Prescription of Chemotherapy Based on Assessment of mRNA Expression of BRCA1, RRM1, ERCC1, TOP1, TOP2α, TUBβ3, TYMS, and GSTP1 Genes in Tumors Compared to Standard Chemotherapy in the Treatment of Non-Small-Cell Lung Cancer. J Pers Med. 2022; 12(10). PMC: 9605448. DOI: 10.3390/jpm12101647. View

4.
Yan L, Liu Z, Wu M, Ge Y, Zhang Q . Effect of lncRNA MALAT1 expression on survival status of elderly patients with severe pneumonia. Eur Rev Med Pharmacol Sci. 2020; 24(7):3959-3964. DOI: 10.26355/eurrev_202004_20865. View

5.
Harrell Jr F, Lee K, Mark D . Multivariable prognostic models: issues in developing models, evaluating assumptions and adequacy, and measuring and reducing errors. Stat Med. 1996; 15(4):361-87. DOI: 10.1002/(SICI)1097-0258(19960229)15:4<361::AID-SIM168>3.0.CO;2-4. View