COT drives resistance to RAF inhibition through MAP kinase pathway reactivation

2010 Nature 1,436 citations

Abstract

Oncogenic mutations in the serine/threonine kinase B-RAF (also known as BRAF) are found in 50–70% of malignant melanomas. Pre-clinical studies have demonstrated that the B-RAF(V600E) mutation predicts a dependency on the mitogen-activated protein kinase (MAPK) signalling cascade in melanoma—an observation that has been validated by the success of RAF and MEK inhibitors in clinical trials. However, clinical responses to targeted anticancer therapeutics are frequently confounded by de novo or acquired resistance. Identification of resistance mechanisms in a manner that elucidates alternative ‘druggable’ targets may inform effective long-term treatment strategies. Here we expressed ∼600 kinase and kinase-related open reading frames (ORFs) in parallel to interrogate resistance to a selective RAF kinase inhibitor. We identified MAP3K8 (the gene encoding COT/Tpl2) as a MAPK pathway agonist that drives resistance to RAF inhibition in B-RAF(V600E) cell lines. COT activates ERK primarily through MEK-dependent mechanisms that do not require RAF signalling. Moreover, COT expression is associated with de novo resistance in B-RAF(V600E) cultured cell lines and acquired resistance in melanoma cells and tissue obtained from relapsing patients following treatment with MEK or RAF inhibitors. We further identify combinatorial MAPK pathway inhibition or targeting of COT kinase activity as possible therapeutic strategies for reducing MAPK pathway activation in this setting. Together, these results provide new insights into resistance mechanisms involving the MAPK pathway and articulate an integrative approach through which high-throughput functional screens may inform the development of novel therapeutic strategies.

Keywords

MelanomaCancer researchKinaseMutationAcquired resistanceDownregulation and upregulationMAPK/ERK pathwayProtein kinase ABiologyGeneNeuroblastoma RAS viral oncogene homologMedicineCancerGeneticsKRAS

MeSH Terms

Allosteric RegulationCell LineTumorClinical Trials as TopicDrug ResistanceNeoplasmEnzyme ActivationGene Expression ProfilingGene Expression RegulationNeoplasticGene LibraryHumansIndolesMAP Kinase Kinase KinasesMAP Kinase Signaling SystemMelanomaMitogen-Activated Protein Kinase KinasesMitogen-Activated Protein KinasesOpen Reading FramesProtein Kinase InhibitorsProto-Oncogene ProteinsProto-Oncogene Proteins B-rafProto-Oncogene Proteins c-rafSulfonamidesVemurafenib

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Publication Info

Year
2010
Type
article
Volume
468
Issue
7326
Pages
968-972
Citations
1436
Access
Closed

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1436
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22
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1236
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Cite This

Cory M. Johannessen, Jesse S. Boehm, So Young Kim et al. (2010). COT drives resistance to RAF inhibition through MAP kinase pathway reactivation. Nature , 468 (7326) , 968-972. https://doi.org/10.1038/nature09627

Identifiers

DOI
10.1038/nature09627
PMID
21107320
PMCID
PMC3058384

Data Quality

Data completeness: 86%