| Literature DB >> 26810603 |
Philip Eliades1,2, David M Miller1,3, Benchun Miao1, Raj Kumar1, Michael Taylor1, Shama Buch4, Sreesha P Srinivasa4, Keith T Flaherty5, Hensin Tsao1.
Abstract
Nearly 100% of melanomas have a defect in the p16(INK4A):cyclin D-CDK4/6:RB pathway, leading to abnormal cell cycle control and unregulated cellular proliferation. Here, we report that P1446A-05, a novel multi-CDK inhibitor has significant inhibitory activity against cutaneous and uveal melanoma. Mechanistic studies revealed that P1446A-05 inhibits phosphorylation targets of CDK members, and induces cell cycle arrest and apoptosis irrespective of melanoma genotype or phenotype. Additionally, we show preclinical evidence that P1446A-05 can synergize with other small molecule inhibitors previously studied in melanoma. Collectively, these data demonstrate that targeting cell cycle and transcriptional CDKs with a small molecule multi-CDK inhibitor is a viable approach for developing novel anti-melanoma therapeutics.Entities:
Keywords: Cell cycle; MAPK pathways; melanoma, multi-CDK inhibitor; synergy
Mesh:
Substances:
Year: 2016 PMID: 26810603 PMCID: PMC4970529 DOI: 10.1080/15384047.2016.1139267
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742