Regulation of alternative splicing of CD44 in cancer
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
25025570
DOI
10.1016/j.cellsig.2014.07.011
PII: S0898-6568(14)00230-7
Knihovny.cz E-resources
- Keywords
- Alternative splicing, CD44, CD44v, CSC, EMT, Isoform switch,
- MeSH
- Alternative Splicing MeSH
- Hyaluronan Receptors genetics metabolism MeSH
- Epithelial-Mesenchymal Transition MeSH
- Humans MeSH
- Neoplastic Stem Cells metabolism MeSH
- Neoplasms metabolism pathology MeSH
- Protein Isoforms genetics metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Hyaluronan Receptors MeSH
- Protein Isoforms MeSH
CD44 is a hyaluronan binding cell surface signal transducing receptor that influences motility, cell survival and proliferation as well as the formation of tumor microenvironment. CD44 contains two variable regions encoded by variable exons. Alternative splicing, which is often deregulated in cancer, can produce various isoforms of CD44 with properties that may have different tissue specific effects and therefore even diverse effects on cancer progression. This review summarizes and puts together all major regulators of alternative splicing of CD44 in cancer that have been documented so far and that have an experimentally proved effect on CD44 isoform switching. It is important to better understand the mechanisms of alternative splicing of CD44, where all the variability of CD44 originates, to be able to explain the isoform switching and occurrence of variant isoforms of CD44 (CD44v) in cancer.
References provided by Crossref.org
Altered Expression of MBNL Family of Alternative Splicing Factors in Colorectal Cancer
Overexpression of CD44v8-10 in Colon Polyps-A Possible Key to Early Diagnosis