BCL-XL inhibitors enhance the apoptotic efficacy of BRAF inhibitors in BRAFV600E colorectal cancer

• Published in: Cell death & disease 2024-03, Vol.15 (3), p.183-183, Article 183
• Main Authors: Jenkins, Laura J., Luk, Ian Y., Chionh, Fiona, Tan, Tao, Needham, Kristen, Ayton, Jamieson, Reehorst, Camilla M., Vukelic, Natalia, Sieber, Oliver M., Mouradov, Dmitri, Gibbs, Peter, Williams, David S., Tebbutt, Niall C., Desai, Jayesh, Hollande, Frédéric, Dhillon, Amardeep S., Lee, Erinna F., Merino, Delphine, Fairlie, W. Douglas, Mariadason, John M.
• Format: Article
• Language: English
• Subjects: 13/2; 13/31; 13/51; 42/41; 45/61; 631/67/1059/602; 631/67/1504/1885/1393; 64/60; 96/106; Antibodies; Apoptosis; Bcl-2 protein; Bcl-x protein; BIM protein; Biochemistry; Biomedical and Life Sciences; Cell Biology; Cell Culture; Colorectal cancer; Colorectal carcinoma; Immunology; Life Sciences; Mcl-1 protein; Medical prognosis; Metastases; Patients; Thrombocytopenia; Toxicity
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-024-06478-z

Metastatic BRAF V600E colorectal cancer (CRC) carries an extremely poor prognosis and is in urgent need of effective new treatments. While the BRAF V600E inhibitor encorafenib in combination with the EGFR inhibitor cetuximab (Enc+Cet) was recently approved for this indication, overall survival is only increased by 3.6 months and objective responses are observed in only 20% of patients. We have found that a limitation of Enc+Cet treatment is the failure to efficiently induce apoptosis in BRAF V600E CRCs, despite inducing expression of the pro-apoptotic protein BIM and repressing expression of the pro-survival protein MCL-1. Here, we show that BRAF V600E CRCs express high basal levels of the pro-survival proteins MCL-1 and BCL-X L , and that combining encorafenib with a BCL-X L inhibitor significantly enhances apoptosis in BRAF V600E CRC cell lines. This effect was partially dependent on the induction of BIM, as BIM deletion markedly attenuated BRAF plus BCL-X L inhibitor-induced apoptosis. As thrombocytopenia is an established on-target toxicity of BCL-X L inhibition, we also examined the effect of combining encorafenib with the BCL-X L -targeting PROTAC DT2216, and the novel BCL-2/BCL-X L inhibitor dendrimer conjugate AZD0466. Combining encorafenib with DT2216 significantly increased apoptosis induction in vitro, while combining encorafenib with AZD0466 was well tolerated in mice and further reduced growth of BRAF V600E CRC xenografts compared to either agent alone. Collectively, these findings demonstrate that combined BRAF and BCL-X L inhibition significantly enhances apoptosis in pre-clinical models of BRAF V600E CRC and is a combination regimen worthy of clinical investigation to improve outcomes for these patients.