[HTML][HTML] Concurrent MEK targeted therapy prevents MAPK pathway reactivation during BRAFV600E targeted inhibition in a novel syngeneic murine glioma model

S Grossauer, K Koeck, NE Murphy, ID Meyers… - Oncotarget, 2016 - ncbi.nlm.nih.gov
Abstract Inhibitors of BRAF V600E kinase are currently under investigations in preclinical
and clinical studies involving BRAF V600E glioma. Studies demonstrated clinical response …

Combined BRAFV600E and MEK blockade for BRAFV600E-mutant gliomas

J Zhang, TW Yao, R Hashizume, S Hariono… - Journal of Neuro …, 2017 - Springer
Abstract BRAF V600E is a common finding in glioma (about 10–60% depending on
histopathologic subclassification). BRAF V600E monotherapy shows modest preclinical …

[HTML][HTML] Regression of BRAFV600E mutant adult glioblastoma after primary combined BRAF-MEK inhibitor targeted therapy: a report of two cases

PYM Woo, TC Lam, JKS Pu, LF Li, RCY Leung… - Oncotarget, 2019 - ncbi.nlm.nih.gov
Background Up to 15% of young adults with glioblastoma have the activating oncogenic
BRAF V600E mutation, an actionable target of the MAPK signal transduction pathway …

BRAF status in personalizing treatment approaches for pediatric gliomas

A Olow, S Mueller, X Yang, R Hashizume… - Clinical Cancer …, 2016 - AACR
Purpose: Alteration of the BRAF/MEK/MAPK pathway is the hallmark of pediatric low-grade
gliomas (PLGGs), and mTOR activation has been documented in the majority of these …

[HTML][HTML] EGFR blockade prevents glioma escape from BRAFV600E targeted therapy

TW Yao, J Zhang, M Prados, WA Weiss, CD James… - Oncotarget, 2015 - ncbi.nlm.nih.gov
Mutational activation of BRAF (BRAF V600E) occurs in pediatric glioma and drives aberrant
MAPK signaling independently of upstream cues. Targeted monotherapy against BRAF …

[HTML][HTML] Acquired resistance to BRAF inhibition in BRAFV600E mutant gliomas

TW Yao, J Zhang, M Prados, WA Weiss, CD James… - Oncotarget, 2017 - ncbi.nlm.nih.gov
Activating mutation of BRAF is a common finding in pediatric gliomas. As many as 14% of
high grade and up to 66% of certain subtypes of low grade pediatric glioma have the BRAF …

PI3′-Kinase Inhibition Forestalls the Onset of MEK1/2 Inhibitor Resistance in BRAF-Mutated Melanoma

MM Deuker, V Marsh Durban, WA Phillips, M McMahon - Cancer discovery, 2015 - AACR
Abstract Phosphatidylinositide 3′(PI3′)-lipid signaling cooperates with oncogenic
BRAFV600E to promote melanomagenesis. Sustained PI3′-lipid production commonly …

[HTML][HTML] Histological transformation to gliosarcoma with combined BRAF/MEK inhibition in BRAF V600E mutated glioblastoma

BE Nelson, NK Reddy, JT Huse, B Amini… - NPJ Precision …, 2023 - nature.com
The identification of BRAF V600 mutation in multiple cancers beyond melanoma and the
development of combined BRAF and MEK targeting agents have altered the landscape of …

[HTML][HTML] Targeting the cyclin dependent kinase and retinoblastoma axis overcomes standard of care resistance in BRAFV600E-mutant melanoma

AL Harris, SE Lee, LK Dawson, LA Marlow… - Oncotarget, 2018 - ncbi.nlm.nih.gov
Patient-derived tumor xenograft (PDTX) mouse models were used to discover new therapies
for naïve and drug resistant BRAF V600E-mutant melanoma. Tumor histology, oncogenic …

[HTML][HTML] BRAFV600E kinase domain duplication identified in therapy-refractory melanoma patient-derived xenografts

K Kemper, O Krijgsman, X Kong… - Cell reports, 2016 - cell.com
The therapeutic landscape of melanoma is improving rapidly. Targeted inhibitors show
promising results, but drug resistance often limits durable clinical responses. There is a …