In a recent paper, Poulikakos et al. describe a new and potentially common mechanism whereby melanomas develop resistance to the BRAF inhibitor vemurafenib by expressing truncated forms of BRAF(V600E) that can dimerize in the absence of activated RAS. Will it be possible to block this with improved BRAF inhibitor design
Activated RAS promotes dimerization of members of the RAF kinase family. ATP-competitive RAF inhibit...
In cases of metastatic melanoma, BRAF is frequently mutated to the V600E oncoprotein causing uncontr...
SummaryCombined BRAF- and MEK-targeted therapy improves upon BRAF inhibitor (BRAFi) therapy but is s...
In a recent paper, Poulikakos et al. describe a new and potentially common mechanism whereby melanom...
SummaryDespite the development of potent RAF/mitogen-activated protein kinase (MAPK) pathway inhibit...
The BRAF kinase, within the mitogen activated protein kinase (MAPK) signaling pathway, harbors activ...
Current BRAF inhibitors block signaling from monomeric BRAFV600E, but not from oncogenic RAS, which ...
SummaryLY3009120 is a pan-RAF and RAF dimer inhibitor that inhibits all RAF isoforms and occupies bo...
The BRAF inhibitors vemurafenib and dabrafenib can be used to treat patients with metastatic melanom...
ERK pathway activation in cells expressing wild-type BRAF is a well-reported, clinically-relevant ad...
ABSTRACT BRAF is a notable oncoprotein within the MAPK signaling pathway, which is a pathway that se...
BRAF is a notable oncoprotein within the MAPK signaling pathway, which is a pathway that sends a sig...
The serine/threonine kinase, BRAF, is mutated in 7% of cancers and 50% of melanomas. The majority of...
SummaryIntravital imaging of BRAF-mutant melanoma cells containing an ERK/MAPK biosensor reveals how...
RAF inhibitors have the unique property of transactivating RAS-dependent RAF dimers in most cells bu...
Activated RAS promotes dimerization of members of the RAF kinase family. ATP-competitive RAF inhibit...
In cases of metastatic melanoma, BRAF is frequently mutated to the V600E oncoprotein causing uncontr...
SummaryCombined BRAF- and MEK-targeted therapy improves upon BRAF inhibitor (BRAFi) therapy but is s...
In a recent paper, Poulikakos et al. describe a new and potentially common mechanism whereby melanom...
SummaryDespite the development of potent RAF/mitogen-activated protein kinase (MAPK) pathway inhibit...
The BRAF kinase, within the mitogen activated protein kinase (MAPK) signaling pathway, harbors activ...
Current BRAF inhibitors block signaling from monomeric BRAFV600E, but not from oncogenic RAS, which ...
SummaryLY3009120 is a pan-RAF and RAF dimer inhibitor that inhibits all RAF isoforms and occupies bo...
The BRAF inhibitors vemurafenib and dabrafenib can be used to treat patients with metastatic melanom...
ERK pathway activation in cells expressing wild-type BRAF is a well-reported, clinically-relevant ad...
ABSTRACT BRAF is a notable oncoprotein within the MAPK signaling pathway, which is a pathway that se...
BRAF is a notable oncoprotein within the MAPK signaling pathway, which is a pathway that sends a sig...
The serine/threonine kinase, BRAF, is mutated in 7% of cancers and 50% of melanomas. The majority of...
SummaryIntravital imaging of BRAF-mutant melanoma cells containing an ERK/MAPK biosensor reveals how...
RAF inhibitors have the unique property of transactivating RAS-dependent RAF dimers in most cells bu...
Activated RAS promotes dimerization of members of the RAF kinase family. ATP-competitive RAF inhibit...
In cases of metastatic melanoma, BRAF is frequently mutated to the V600E oncoprotein causing uncontr...
SummaryCombined BRAF- and MEK-targeted therapy improves upon BRAF inhibitor (BRAFi) therapy but is s...