Details

Autor(en) / Beteiligte

• Jenkins, Laura J
• Luk, Ian Y
• Fairlie, W Douglas
• Lee, Erinna F
• Palmieri, Michelle
• Schoffer, Kael L
• Tan, Tao
• Ng, Irvin
• Vukelic, Natalia
• Tran, Sharon
• Tse, Janson W T
• Nightingale, Rebecca
• Alam, Zakia
• Chionh, Fiona
• Iatropoulos, George
• Ernst, Matthias
• Afshar-Sterle, Shoukat
• Desai, Jayesh
• Gibbs, Peter
• Sieber, Oliver M
• Dhillon, Amardeep S
• Tebbutt, Niall C
• Mariadason, John M

Titel

Genotype-Tailored ERK/MAPK Pathway and HDAC Inhibition Rewires the Apoptotic Rheostat to Trigger Colorectal Cancer Cell Death

Ist Teil von

• Molecular cancer therapeutics, 2023-01, Vol.22 (1), p.52-62

Ort / Verlag

United States: American Association for Cancer Research

Erscheinungsjahr

2023

Quelle

MEDLINE

Beschreibungen/Notizen

• The EGFR/RAS/MEK/ERK signaling pathway (ERK/MAPK) is hyperactivated in most colorectal cancers. A current limitation of inhibitors of this pathway is that they primarily induce cytostatic effects in colorectal cancer cells. Nevertheless, these drugs do induce expression of proapoptotic factors, suggesting they may prime colorectal cancer cells to undergo apoptosis. As histone deacetylase inhibitors (HDACis) induce expression of multiple proapoptotic proteins, we examined whether they could synergize with ERK/MAPK inhibitors to trigger colorectal cancer cell apoptosis. Combined MEK/ERK and HDAC inhibition synergistically induced apoptosis in colorectal cancer cell lines and patient-derived tumor organoids in vitro, and attenuated Apc-initiated adenoma formation in vivo. Mechanistically, combined MAPK/HDAC inhibition enhanced expression of the BH3-only proapoptotic proteins BIM and BMF, and their knockdown significantly attenuated MAPK/HDAC inhibitor-induced apoptosis. Importantly, we demonstrate that the paradigm of combined MAPK/HDAC inhibitor treatment to induce apoptosis can be tailored to specific MAPK genotypes in colorectal cancers, by combining an HDAC inhibitor with either an EGFR, KRASG12C or BRAFV600 inhibitor in KRAS/BRAFWT; KRASG12C, BRAFV600E colorectal cancer cell lines, respectively. These findings identify a series of ERK/MAPK genotype-tailored treatment strategies that can readily undergo clinical testing for the treatment of colorectal cancer.