» Articles » PMID: 33849532

Identification of Genes and Pathways Involved in Malignant Pleural Mesothelioma Using Bioinformatics Methods

Overview
Publisher Biomed Central
Specialty Genetics
Date 2021 Apr 14
PMID 33849532
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Malignant pleural mesothelioma (MPM) is a rare tumor in the pleura. This study was carried out to identify key genes and pathways that may be involved in MPM.

Methods: Microarray datasets GSE51024 and GSE2549 were analyzed for differentially expressed genes (DEGs) between normal and MPM tissues. The identified DEGs were subjected to functional analyses using bioinformatics tools.

Results: A total of 276 DEGs were identified, consisting of 187 downregulated and 79 upregulated genes. Gene ontology and Kyoto encyclopedia of genes and genomes pathway enrichment analysis indicated that the DEGs were enriched in extracellular structure organization, extracellular matrix, and ECM-receptor interaction. Due to high degree of connectivity among 24 hub genes, EZH2 and HMMR are likely to play roles in the carcinogenesis and progression of MPM. The two genes were found over-expressed in MPM tissues. Patients with elevated EZH2 and HMMR expressions had poor overall survival.

Conclusions: EZH2 and HMMR are identified to be the hub genes for MPM and they may be further characterized to better understand the molecular mechanisms underlying the carcinogenesis of MPM.

Citing Articles

Comprehensive Analysis Identifies Hyaluronan Mediated Motility Receptor and Cell Division Cycle 25C as Potential Prognostic Biomarkers in Head and Neck Squamous Cell Carcinoma.

Zhang H, Xu Y, Han H, Ye X, Cheng L, Shen Y Cancer Control. 2024; 31:10732748241287904.

PMID: 39323031 PMC: 11440566. DOI: 10.1177/10732748241287904.


Benefits and Challenges of Inhibiting EZH2 in Malignant Pleural Mesothelioma.

Al Khatib M, Pinton G, Moro L, Porta C Cancers (Basel). 2023; 15(5).

PMID: 36900330 PMC: 10000483. DOI: 10.3390/cancers15051537.


Advances in Immunotherapy of Malignant Pleural Mesothelioma.

Liao D, Yu Y, Mei Q, Wang Z, Li X, Jia Y Onco Targets Ther. 2021; 14:4477-4484.

PMID: 34429612 PMC: 8374846. DOI: 10.2147/OTT.S317434.


A network-biology approach for identification of key genes and pathways involved in malignant peritoneal mesothelioma.

Mahfuz A, Zubair-Bin-Mahfuj A, Podder D Genomics Inform. 2021; 19(2):e16.

PMID: 34261301 PMC: 8261271. DOI: 10.5808/gi.21019.


Pathological Characterization of Tumor Immune Microenvironment (TIME) in Malignant Pleural Mesothelioma.

Napoli F, Listi A, Zambelli V, Witel G, Bironzo P, Papotti M Cancers (Basel). 2021; 13(11).

PMID: 34073720 PMC: 8197227. DOI: 10.3390/cancers13112564.

References
1.
LaFave L, Beguelin W, Koche R, Teater M, Spitzer B, Chramiec A . Loss of BAP1 function leads to EZH2-dependent transformation. Nat Med. 2015; 21(11):1344-9. PMC: 4636469. DOI: 10.1038/nm.3947. View

2.
Kaarteenaho-Wiik R, Soini Y, Pollanen R, Paakko P, Kinnula V . Over-expression of tenascin-C in malignant pleural mesothelioma. Histopathology. 2003; 42(3):280-91. DOI: 10.1046/j.1365-2559.2003.01568.x. View

3.
Suveg K, Putora P, Berghmans T, Glatzer M, Kovac V, Cihoric N . Current efforts in research of pleural mesothelioma-An analysis of the ClinicalTrials.gov registry. Lung Cancer. 2018; 124:12-18. DOI: 10.1016/j.lungcan.2018.07.007. View

4.
Leong S, Zainudin R, Kazan-Allen L, Robinson B . Asbestos in Asia. Respirology. 2015; 20(4):548-55. DOI: 10.1111/resp.12517. View

5.
Bueno R, Stawiski E, Goldstein L, Durinck S, De Rienzo A, Modrusan Z . Comprehensive genomic analysis of malignant pleural mesothelioma identifies recurrent mutations, gene fusions and splicing alterations. Nat Genet. 2016; 48(4):407-16. DOI: 10.1038/ng.3520. View