Details

Autor(en) / Beteiligte

• Wyce, Anastasia
• Matteo, Jeanne J.
• Foley, Shawn W.
• Felitsky, Daniel J.
• Rajapurkar, Satyajit R.
• Zhang, Xi-Ping
• Musso, Melissa C.
• Korenchuk, Susan
• Karpinich, Natalie O.
• Keenan, Kathryn M.
• Stern, Melissa
• Mathew, Lijoy K.
• McHugh, Charles F.
• McCabe, Michael T.
• Tummino, Peter J.
• Kruger, Ryan G.
• Carpenter, Christopher
• Barbash, Olena

Titel

MEK inhibitors overcome resistance to BET inhibition across a number of solid and hematologic cancers

Ist Teil von

• Oncogenesis (New York, NY), 2018-04, Vol.7 (4), p.35-12, Article 35

Ort / Verlag

London: Nature Publishing Group UK

Erscheinungsjahr

2018

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• BET inhibitors exhibit broad activity in cancer models, making predictive biomarkers challenging to define. Here we investigate the biomarkers of activity of the clinical BET inhibitor GSK525762 (I-BET; I-BET762) across cancer cell lines and demonstrate that KRAS mutations are novel resistance biomarkers. This finding led us to combine BET with RAS pathway inhibition using MEK inhibitors to overcome resistance, which resulted in synergistic effects on growth and survival in RAS pathway mutant models as well as a subset of cell lines lacking RAS pathway mutations. GSK525762 treatment up-regulated p-ERK1/2 levels in both RAS pathway wild-type and mutant cell lines, suggesting that MEK/ERK pathway activation may also be a mechanism of adaptive BET inhibitor resistance. Importantly, gene expression studies demonstrated that the BET/MEK combination uniquely sustains down-regulation of genes associated with mitosis, leading to prolonged growth arrest that is not observed with either single agent therapy. These studies highlight a potential to enhance the clinical benefit of BET and MEK inhibitors and provide a strong rationale for clinical evaluation of BET/MEK combination therapies in cancer.