[HTML][HTML] The BRD9/7 inhibitor TP-472 blocks melanoma tumor growth by suppressing ECM-mediated oncogenic signaling and inducing apoptosis

LD Mason, S Chava, KK Reddi, R Gupta - Cancers, 2021 - mdpi.com
Simple Summary Melanoma is an aggressive form of skin cancer and the leading cause of
skin cancer-related deaths. Current therapies, including those targeting oncogenic pathways …

BRD4 is a novel therapeutic target in melanoma

MF Segura, RD Micco, G Zhang, W Zhang, I Osman… - Cancer Research, 2012 - AACR
The incidence of melanoma is increasing faster than that of any other cancer, and predicted
to double every 10-20 years. Surgery can be curative in Stage I, II, or III disease, but 75% of …

BET and BRAF inhibitors act synergistically against BRAF‐mutant melanoma

L Paoluzzi, D Hanniford, E Sokolova, I Osman… - Cancer …, 2016 - Wiley Online Library
Despite major advances in the treatment of metastatic melanoma, treatment failure is still
inevitable in most cases. Manipulation of key epigenetic regulators, including inhibition of …

[PDF][PDF] Harnessing BET inhibitor sensitivity reveals AMIGO2 as a melanoma survival gene

B Fontanals-Cirera, D Hasson, C Vardabasso… - Molecular cell, 2017 - cell.com
Bromodomain and extraterminal domain inhibitors (BETi) represent promising therapeutic
agents for metastatic melanoma, yet their mechanism of action remains unclear. Here we …

BRD4 sustains melanoma proliferation and represents a new target for epigenetic therapy

MF Segura, B Fontanals-Cirera, A Gaziel-Sovran… - Cancer research, 2013 - AACR
Metastatic melanoma remains a mostly incurable disease. Although newly approved
targeted therapies are efficacious in a subset of patients, resistance and relapse rapidly …

Biomarker accessible and chemically addressable mechanistic subtypes of BRAF melanoma

B Eskiocak, EA McMillan, S Mendiratta, RK Kollipara… - Cancer discovery, 2017 - AACR
Genomic diversity among melanoma tumors limits durable control with conventional and
targeted therapies. Nevertheless, pathologic activation of the ERK1/2 pathway is a linchpin …

[HTML][HTML] GZ17-6.02 interacts with [MEK1/2 and B-RAF inhibitors] to kill melanoma cells

L Booth, C West, D Von Hoff, JM Kirkwood… - Frontiers in …, 2021 - frontiersin.org
We defined the lethal interaction between the novel therapeutic GZ17-6.02 and the standard
of care combination of the MEK1/2 inhibitor trametinib and the B-RAF inhibitor dabrafenib in …

Co‐targeting BET and MEK as salvage therapy for MAPK and checkpoint inhibitor‐resistant melanoma

IM Echevarría‐Vargas, PI Reyes‐Uribe… - EMBO molecular …, 2018 - embopress.org
Despite novel therapies for melanoma, drug resistance remains a significant hurdle to
achieving optimal responses. NRAS‐mutant melanoma is an archetype of therapeutic …

[HTML][HTML] BET inhibitors synergize with sunitinib in melanoma through GDF15 suppression

F Zeng, Y Li, Y Meng, H Sun, Y He, M Yin… - … & Molecular Medicine, 2023 - nature.com
Targeting bromodomain and extra-terminal domain (BET) proteins has shown a promising
therapeutic effect on melanoma. The development of strategies to better kill melanoma cells …

[HTML][HTML] Enhancing therapeutic approaches for melanoma patients targeting epigenetic modifiers

M Gracia-Hernandez, Z Munoz, A Villagra - Cancers, 2021 - mdpi.com
Simple Summary Melanoma affects over 300,000 people worldwide every year. Recent
advancements in therapeutic treatments for melanoma patients, such as targeted therapies …