Comprehensive identification of hub mRNAs and lncRNAs in colorectal cancer using galaxy: an in silico transcriptome analysis

被引:0
作者
Yari, Mohsen [1 ]
Eidi, Milad [2 ,3 ]
Omrani, Mohammad-Amin [4 ]
Fazeli, Zahra [5 ]
Rahmanian, Mohammad [5 ,6 ]
Ghafouri-Fard, Soudeh [5 ]
机构
[1] Rutgers Canc Inst New Jersey, Dept Radiat Oncol, New Brunswick, NJ USA
[2] McGill Univ, Hlth Ctr Res Inst, Child Hlth & Human Dev Program, Endocrine Genet Lab, Montreal, PQ, Canada
[3] Mcgill Univ, Hlth Ctr Res Inst, Dept Pediat, Montreal, PQ, Canada
[4] Shahid Beheshti Univ Med Sci, Urol & Nephrol Res Ctr UNRC, Tehran, Iran
[5] Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
[6] Shahid Beheshti Univ Med Sci, Student Res Comm, Sch Med, Tehran, Iran
关键词
Genes; MRNA; LncRNA; Biomarker; Colorectal cancer; POOR-PROGNOSIS; PROMOTES; INVASION; MIGRATION; OVEREXPRESSION; PROLIFERATION; POPULATION; PROTEINS; DLX6-AS1; GENES;
D O I
10.1007/s12672-025-02026-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is the second leading cause of cancer-related mortality. Using the Galaxy platform, the present study aimed to assess the differentially expressed genes (DEGs) in CRC patients. The expression data was obtained from the Gene Expression Omnibus database (GSE137327). DEGs were analyzed using Gene Ontology (GO) and GeneMANIA databases to detect the most critical biological pathways and processes. Protein-Protein Interaction Studies (PPIS) identified four hub genes (CCN1, CCL2, FLNC, MYH11). This article presents findings on three mRNAs (CEMIP, MMP7, and DPEP1) and also two notable lncRNAs, EVADR and DLX6-AS1, that have an impact on CRC pathogenesis and play a role in the epithelial-mesenchymal transition in tumor cells. The identified genes and lncRNAs are putative therapeutic targets and diagnostic markers. For instance, CRISPR/Cas9 editing systems can be designed in order to modulate expression of these genes, or edit them for the purpose of inducing sensitivity to conventional therapies. Besides, these genes can be incorporated into clinical prognostic models, offering panels of genes to choose appropriate personalized methods of treatment. Together, these genes represent novel markers and possible therapeutic targets for CRC.
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页数:16
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