Drug discovery: How melanomas bypass new therapy

Nature. 2010 Dec 16;468(7326):902-3. doi: 10.1038/468902a.
No abstract available

Publication types

  • News
  • Comment

MeSH terms

  • Drug Resistance, Neoplasm* / drug effects
  • Drug Resistance, Neoplasm* / genetics
  • Enzyme Activation / drug effects
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Indoles / pharmacology
  • Indoles / therapeutic use
  • MAP Kinase Kinase Kinases / genetics
  • MAP Kinase Kinase Kinases / metabolism*
  • MAP Kinase Signaling System* / drug effects
  • Melanoma / drug therapy*
  • Melanoma / enzymology*
  • Melanoma / genetics
  • Melanoma / pathology
  • Mitogen-Activated Protein Kinase Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mutation / genetics
  • Neoplasm Recurrence, Local
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors*
  • Proto-Oncogene Proteins B-raf / chemistry
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins B-raf / metabolism
  • Proto-Oncogene Proteins c-raf / genetics*
  • Proto-Oncogene Proteins c-raf / metabolism
  • Sulfonamides / pharmacology
  • Sulfonamides / therapeutic use
  • Vemurafenib

Substances

  • Indoles
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins
  • Sulfonamides
  • Vemurafenib
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • Proto-Oncogene Proteins c-raf
  • Extracellular Signal-Regulated MAP Kinases
  • MAP Kinase Kinase Kinases
  • MAP3K8 protein, human
  • Mitogen-Activated Protein Kinase Kinases