Title : Cooperativity of Cdk4R24C and Ras in melanoma development.

Pub. Date : 2010 Aug 15

PMID : 20703083






5 Functional Relationships(s)
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1 Treatment of Tyr-HRas:Cdk4(R24C/R24C) mice with the carcinogen, DMBA/TPA resulted in a further increase in the number of nevi and melanomas developed when compared with Tyr-HRas:Cdk4(+/+) mice. Tyrosine Harvey rat sarcoma virus oncogene Mus musculus
2 Treatment of Tyr-HRas:Cdk4(R24C/R24C) mice with the carcinogen, DMBA/TPA resulted in a further increase in the number of nevi and melanomas developed when compared with Tyr-HRas:Cdk4(+/+) mice. Tyrosine Harvey rat sarcoma virus oncogene Mus musculus
3 Treatment of Tyr-HRas:Cdk4(R24C/R24C) mice with the carcinogen, DMBA/TPA resulted in a further increase in the number of nevi and melanomas developed when compared with Tyr-HRas:Cdk4(+/+) mice. Tyrosine Harvey rat sarcoma virus oncogene Mus musculus
4 In summary, in Tyr-HRas:Cdk4(R24C/R24C) mice, we observed that activated CDK4 cooperates with the oncogenic HRAS(G12V) protein to increase the susceptibility of melanoma development in vivo. Tyrosine Harvey rat sarcoma virus oncogene Mus musculus
5 In summary, in Tyr-HRas:Cdk4(R24C/R24C) mice, we observed that activated CDK4 cooperates with the oncogenic HRAS(G12V) protein to increase the susceptibility of melanoma development in vivo. Tyrosine Harvey rat sarcoma virus oncogene Mus musculus