Implications of Genetic and Epigenetic Alterations of CDKN2A (p16(INK4a)) in Cancer.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 27428416.
- Also identified by DOI 10.1016/j.ebiom.2016.04.017 and PMC identifier 4919535.
- Licence recorded as CC BY-NC-ND.
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Abstract
Aberrant gene silencing is highly associated with altered cell cycle regulation during carcinogenesis. In particular, silencing of the CDKN2A tumor suppressor gene, which encodes the p16(INK4a) protein, has a causal link with several different types of cancers. The p16(INK4a) protein plays an executional role in cell cycle and senescence through the regulation of the cyclin-dependent kinase (CDK) 4/6 and cyclin D complexes. Several genetic and epigenetic aberrations of CDKN2A lead to enhanced tumorigenesis and metastasis with recurrence of cancer and poor prognosis. In these cases, the restoration of genetic and epigenetic reactivation of CDKN2A is a practical approach for the prevention and therapy of cancer. This review highlights the genetic status of CDKN2A as a prognostic and predictive biomarker in various cancers.
Medical subject headings
- Cyclin-Dependent Kinase Inhibitor p16
- Epigenesis, Genetic