Molecular targeting of the BRAF proto-oncogene/mitogen-activated protein kinase (MAPK) pathway across cancers

KS Shan, TU Rehman, S Ivanov, G Domingo… - International Journal of …, 2024 - mdpi.com
The mitogen-activated protein kinase (MAPK) pathway is essential for cellular proliferation,
growth, and survival. Constitutive activation of this pathway by BRAF mutations can cause …

Therapeutic strategies for inhibiting oncogenic BRAF signaling

E Halilovic, DB Solit - Current opinion in pharmacology, 2008 - Elsevier
Mitogen-activated protein kinase (MAPK) activation is a common property of human cancers
and is often due to activating mutations in the BRAF and RAS genes. BRAF kinase domain …

Targeting oncogenic BRAF in human cancer

CA Pratilas, F Xing, DB Solit - Therapeutic Kinase Inhibitors, 2011 - Springer
Abstract Mitogen Activated Protein Kinase (MAPK) pathway activation is a frequent event in
human cancer and is often the result of activating mutations in the BRAF and RAS …

BRAF as therapeutic target in melanoma

C Wellbrock, A Hurlstone - Biochemical pharmacology, 2010 - Elsevier
BRAF is a member of the RAF kinase family, which acts in the ERK/MAP kinase pathway, a
signalling cascade that regulates cellular proliferation, differentiation and survival. Single …

BRAF as a target for cancer therapy

R Dienstmann, J Tabernero - Anti-Cancer Agents in Medicinal …, 2011 - ingentaconnect.com
Tumors with mutations in the gene encoding the serine-threonine protein kinase BRAF are
dependent on the MAPK signaling pathway for their growth, what offers an opportunity to test …

Mechanism of BRAF activation through biochemical characterization of the recombinant full‐length protein

N Cope, C Candelora, K Wong, S Kumar, H Nan… - …, 2018 - Wiley Online Library
BRAF kinase plays an important role in mitogen‐activated protein kinase (MAPK) signaling
and harbors activating mutations in about half of melanomas and in a smaller percentage in …

Recent progress in the identification of BRAF inhibitors as anti-cancer agents

HB El-Nassan - European Journal of Medicinal Chemistry, 2014 - Elsevier
Abstract The “RAS/BRAF/MEK/ERK” pathway has been associated with human cancers due
to the frequent oncogenic mutations identified in its members. In particular, BRAF is mutated …

[HTML][HTML] BRAF mutation in progression and therapy of melanoma, papillary thyroid carcinoma and colorectal adenocarcinoma

I Zaleśna, ML Hartman, M Czyż - Advances in Hygiene and Experimental …, 2016 - phmd.pl
BRAF is mutated at a high frequency in various malignancies, including melanoma, papillary
thyroid carcinoma and colorectal adenocarcinoma. BRAF is an element of the …

Tumor Cell Resistance to the Inhibition of BRAF and MEK1/2

W Chen, JI Park - International Journal of Molecular Sciences, 2023 - mdpi.com
BRAF is one of the most frequently mutated oncogenes, with an overall frequency of about
50%. Targeting BRAF and its effector mitogen-activated protein kinase kinase 1/2 (MEK1/2) …

[HTML][HTML] Precision oncology for BRAF-mutant cancers with BRAF and MEK inhibitors: from melanoma to tissue-agnostic therapy

MA Gouda, V Subbiah - ESMO open, 2023 - Elsevier
Highlights•BRAF alterations lead to unbridled activation of the MAPK pathway which can
result in cancer development and progression.•BRAF and MEK inhibitors led to paradigm …