Transcriptome Profiling of Mouse Embryonic Fibroblast Spontaneous Immortalization: A Comparative Analysis.
Jocshan Loaiza-MossUrsula BraunMichael LeitgesPublished in: International journal of molecular sciences (2024)
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 .
Keyphrases
- genome wide
- network analysis
- single cell
- protein protein
- bioinformatics analysis
- dna methylation
- rna seq
- genome wide identification
- poor prognosis
- immune response
- cell adhesion
- signaling pathway
- small molecule
- copy number
- induced apoptosis
- gene expression
- genome wide analysis
- papillary thyroid
- cell cycle arrest
- electronic health record
- transcription factor
- squamous cell carcinoma
- pi k akt
- toll like receptor
- machine learning
- cell proliferation
- bone marrow
- inflammatory response
- mesenchymal stem cells
- cell therapy
- artificial intelligence
- human health
- endoplasmic reticulum stress
- data analysis