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Disclosing Potential Key Genes, Therapeutic Targets and Agents for Non-Small Cell Lung Cancer: Evidence from Integrative Bioinformatics Analysis

文献类型:期刊论文

作者Mosharaf, Md Parvez1,5; Reza, Md Selim2,5; Gov, Esra3; Mahumud, Rashidul Alam4; Mollah, Md Nurul Haque5
刊名VACCINES
出版日期2022-05-01
卷号10期号:5页码:20
关键词non-small cell lung cancer gene expression profiles molecular signatures therapeutic targets and agents integrated bioinformatics approaches
DOI10.3390/vaccines10050771
英文摘要Non-small-cell lung cancer (NSCLC) is considered as one of the malignant cancers that causes premature death. The present study aimed to identify a few potential novel genes highlighting their functions, pathways, and regulators for diagnosis, prognosis, and therapies of NSCLC by using the integrated bioinformatics approaches. At first, we picked out 1943 DEGs between NSCLC and control samples by using the statistical LIMMA approach. Then we selected 11 DEGs (CDK1, EGFR, F Upsilon N, UBC, M Upsilon C, CCNB1, FOS, RHOB, CDC6, CDC20, and CHEK1) as the hub-DEGs (potential key genes) by the protein-protein interaction network analysis of DEGs. The DEGs and hub-DEGs regulatory network analysis commonly revealed four transcription factors (FOXC1, GATA2, Upsilon Upsilon 1, and NFIC) and five miRNAs (miR-335-5p, miR-26b-5p, miR-92a-3p, miR-155-5p, and miR-16-5p) as the key transcriptional and post-transcriptional regulators of DEGs as well as hub-DEGs. We also disclosed the pathogenetic processes of NSCLC by investigating the biological processes, molecular function, cellular components, and KEGG pathways of DEGs. The multivariate survival probability curves based on the expression of hub-DEGs in the SurvExpress web-tool and database showed the significant differences between the low- and high-risk groups, which indicates strong prognostic power of hub-DEGs. Then, we explored top-ranked 5-hub-DEGs-guided repurposable drugs based on the Connectivity Map (CMap) database. Out of the selected drugs, we validated six FDA-approved launched drugs (Dinaciclib, Afatinib, Icotinib, Bosutinib, Dasatinib, and TWS-119) by molecular docking interaction analysis with the respective target proteins for the treatment against NSCLC. The detected therapeutic targets and repurposable drugs require further attention by experimental studies to establish them as potential biomarkers for precision medicine in NSCLC treatment.
WOS研究方向Immunology ; Research & Experimental Medicine
语种英语
WOS记录号WOS:000803470300001
出版者MDPI
源URL[http://119.78.100.204/handle/2XEOYT63/19576]  
专题中国科学院计算技术研究所期刊论文_英文
通讯作者Mollah, Md Nurul Haque
作者单位1.Univ Southern Queensland, Fac Business Educ Law & Arts, Sch Commerce, Toowoomba, Qld 4350, Australia
2.Chinese Acad Sci, Ctr High Performance Comp, Joint Engn Res Ctr Hlth Big Data Intelligent Anal, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
3.Adana AlparslanTurkes Sci & Technol Univ, Fac Engn, Dept Bioengn, TR-01250 Adana, Turkey
4.Univ Sydney, Fac Med & Hlth, NHMRC Clin Trials Ctr, Camperdown, NSW 2006, Australia
5.Univ Rajshahi, Dept Stat, Bioinformat Lab, Rajshahi 6205, Bangladesh
推荐引用方式
GB/T 7714
Mosharaf, Md Parvez,Reza, Md Selim,Gov, Esra,et al. Disclosing Potential Key Genes, Therapeutic Targets and Agents for Non-Small Cell Lung Cancer: Evidence from Integrative Bioinformatics Analysis[J]. VACCINES,2022,10(5):20.
APA Mosharaf, Md Parvez,Reza, Md Selim,Gov, Esra,Mahumud, Rashidul Alam,&Mollah, Md Nurul Haque.(2022).Disclosing Potential Key Genes, Therapeutic Targets and Agents for Non-Small Cell Lung Cancer: Evidence from Integrative Bioinformatics Analysis.VACCINES,10(5),20.
MLA Mosharaf, Md Parvez,et al."Disclosing Potential Key Genes, Therapeutic Targets and Agents for Non-Small Cell Lung Cancer: Evidence from Integrative Bioinformatics Analysis".VACCINES 10.5(2022):20.

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来源:计算技术研究所

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