Signaling Pathways and Protein-Protein Interaction of Vimentin in Invasive and Migration Cells: A Review.
Danial Hashemi KaroiiHossein AziziMahdi AmirianPublished in: Cellular reprogramming (2022)
The vimentin (encoded by VIM) is one of the 70 human intermediate filaments (IFs), building highly dynamic and cell-type-specific web networks in the cytoplasm. Vim -/- mice exhibit process defects associated with cell differentiation, which can have implications for understanding cancer and disease. This review showed recent reports from studies that unveiled vimentin intermediate filaments (VIFs) as an essential component of the cytoskeleton, followed by a description of vimentin's physiological functions and process reports in VIF signaling pathway and gene network studies. The main focus of the discussion is on vital signaling pathways associated with how VIF coordinates invasion cells and migration. The current research will open up multiple processes to research the function of VIF and other IF proteins in cellular and molecular biology, and they will lead to essential insights into different VIF levels for the invasive metastatic cancer cells. Enrich GO databases used Gene Ontology and Pathway Enrichment Analysis. Estimation with STRING online was to predict the functional and molecular interactions of proteins-protein with Cytoscape analysis to search and select the master genes. Using Cytoscape and STRING analysis, we presented eight genes, RhoA, Smad3, Akt1, Cdk2, Rock1, Rock2, Mapk1, and Mapk8, as the essential protein-protein interaction with vimentin involved in the invasion.
Keyphrases
- signaling pathway
- protein protein
- induced apoptosis
- pi k akt
- small molecule
- cell cycle arrest
- epithelial mesenchymal transition
- genome wide
- oxidative stress
- endothelial cells
- small cell lung cancer
- squamous cell carcinoma
- endoplasmic reticulum stress
- genome wide identification
- single molecule
- dna methylation
- big data
- adipose tissue
- metabolic syndrome
- social media
- papillary thyroid
- skeletal muscle
- cell migration
- machine learning
- bioinformatics analysis
- adverse drug
- amino acid
- electronic health record
- cell death