Transcriptome Profiling of Mouse Embryonic Fibroblast Spontaneous Immortalization: A Comparative Analysis

被引:0
|
作者
Loaiza-Moss, Jocshan [1 ]
Braun, Ursula [1 ]
Leitges, Michael [1 ]
机构
[1] Mem Univ Newfoundland, Fac Med, Div Biomed Sci, 300 Prince Philip Dr, St John, NF A1B 3V6, Canada
关键词
spontaneous cell immortalization; mouse embryonic fibroblast (MEF); RNA-seq; transcriptome profiling; gene regulatory network (GRN); CELL-ADHESION MOLECULES; TUMOR-SUPPRESSOR; GENE-EXPRESSION; CATALYTIC SUBUNIT; SIGNALING PATHWAY; DOWN-REGULATION; THYROID-CANCER; UP-REGULATION; E-CADHERIN; KAPPA-B;
D O I
10.3390/ijms25158116
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell immortalization, a hallmark of cancer development, is a process that cells can undergo on their path to carcinogenesis. Spontaneously immortalized mouse embryonic fibroblasts (MEFs) have been used for decades; however, changes in the global transcriptome during this process have been poorly described. In our research, we characterized the poly-A RNA transcriptome changes after spontaneous immortalization. To this end, differentially expressed genes (DEGs) were screened using DESeq2 and characterized by gene ontology enrichment analysis and protein-protein interaction (PPI) network analysis to identify the potential hub genes. In our study, we identified changes in the expression of genes involved in proliferation regulation, cell adhesion, immune response and transcriptional regulation in immortalized MEFs. In addition, we performed a comparative analysis with previously reported MEF immortalization data, where we propose a predicted gene regulatory network model in immortalized MEFs based on the altered expression of Mapk11, Cdh1, Chl1, Zic1, Hoxd10 and the novel hub genes Il6 and Itgb2.
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页数:20
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