Title : Synergistic inhibition of human melanoma proliferation by combination treatment with B-Raf inhibitor BAY43-9006 and mTOR inhibitor Rapamycin.

Pub. Date : 2005 Oct 28

PMID : 16255777






4 Functional Relationships(s)
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1 Synergistic inhibition of human melanoma proliferation by combination treatment with B-Raf inhibitor BAY43-9006 and mTOR inhibitor Rapamycin. Sorafenib B-Raf proto-oncogene, serine/threonine kinase Homo sapiens
2 Melanoma cells containing the B-Raf mutation V599E were more sensitive than cells with wild-type B-raf to 10 nM doses of both BAY43-9006 and rapamycin. Sorafenib B-Raf proto-oncogene, serine/threonine kinase Homo sapiens
3 Melanoma cells containing the B-Raf mutation V599E were more sensitive than cells with wild-type B-raf to 10 nM doses of both BAY43-9006 and rapamycin. Sorafenib B-Raf proto-oncogene, serine/threonine kinase Homo sapiens
4 As expected, rapamycin inhibited the phosphorylation of mTOR substrates, p70S6K and 4EBP1, and BAY43-9006 inhibited phosphorylation of ERK, which is dependent on B-Raf activity. Sorafenib B-Raf proto-oncogene, serine/threonine kinase Homo sapiens