Journal article
The cell-cycle regulator CDK4: An emerging therapeutic target in melanoma
KE Sheppard, GA McArthur
Clinical Cancer Research | AMER ASSOC CANCER RESEARCH | Published : 2013
Abstract
The recent clinical success of targeted therapies in melanoma directed at the oncogene BRAF validates the concept of targeting oncogenes. The p16-cyclin D-CDK4/6-retinoblastoma protein pathway (CDK4 pathway) is dysregulated in 90% of melanomas, and is, therefore, an obvious therapeutic target for this disease. The main outcome of CDK4 activation is the phosphorylation and, thus, inhibition of the retinoblastoma protein leading to G1-S cell-cycle transition. In addition, CDK4 directly phosphorylates other proteins that promote cell-cycle progression and inhibit both cell senescence and apoptosis. In preclinical studies, the response to CDK4 inhibition correlates with genomic changes that incr..
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Funding Acknowledgements
The work was financially supported by grants from the National Health and Medical Research Council (NHMRC) of Australia grant no. 10002655 to G. A. McArthur and grant no. 1042986 to G. A. McArthur and K. E. Sheppard. G. A. McArthur is a recipient of an NHMRC practitioner fellowship.