← BioTransfer GEO Dataset Finder
GEO series

Inhibition of BCL2 family proteins overcomes acquired resistance to standard of care BRAF and MEK inhibitors in a subset of BRAFV600E-mutant melanomas

GSE298507 Homo sapiens Expression profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing 58 samples 2026/03/30 GPL11154
Summary
Despite recent advances, a significant number of melanoma patients treated with BRAF and MEK targeted therapies (BRAFi/MEKi) or immunotherapies develop progressive disease. Anti-apoptotic BCL family proteins have been shown to promote de novo resistance to a number of therapies, including single-agent BRAF inhibitors in BRAF-mutant melanomas. In this study, in vivo testing of a collection of BRAFi- or BRAFi/MEKi treatment-refractory melanoma patient-derived xenograft (PDX) models showed that combining BCL2 inhibitors (BCL2i, navitoclax or venetoclax) with BRAFi and MEKi surprisingly induced potent regressions of a significant subset of these treatment-refractory PDXs. High basal BCL2 expression correlated with improved sensitivity, while high basal MCL1 predicted resistance to BCL2i combination with BRAFi/MEKi. Studies with MCL1 overexpression functionally validated its role in resistance. Further, combination of BRAFi/MEKi with a MCL1 inhibitor (MCL1i) counteracted the resistance and also decreased MCL1i-associated cardiotoxicity markers.
Download
NCBI GEO page ↗ {# Names what the click gives you. "Open in finder" meant nothing to a visitor who arrived from a search engine and has never seen the tool. #} Find more human RNA-seq datasets →
Similar datasets

Search all human RNA-seq datasets in GEO →

Share this dataset

Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.