Targeting BCL-XL in fibrolamellar hepatocellular carcinoma Journal Article


Authors: Shebl, B.; Ng, D.; Lalazar, G.; Rosemore, C.; Finkelstein, T. M.; Migler, R. D.; Zheng, G.; Zhang, P.; Jiang, C. S.; Qureshi, A.; Vaughan, R.; Yarchoan, M.; de Jong, Y. P.; Rice, C. M.; Coffino, P.; Ortiz, M. V.; Zhou, D.; Simon, S. M.
Article Title: Targeting BCL-XL in fibrolamellar hepatocellular carcinoma
Abstract: Fibrolamellar hepatocellular carcinoma (FLC) is a rare and often lethal liver cancer with no proven effective systemic therapy. Inhibition of the antiapoptotic protein BCL-XL was found to synergize with a variety of systemic therapies in vitro using cells dissociated from patient-derived xenografts (PDX) of FLC or cells dissociated directly from surgical patient resections. As BCL-XL is physiologically expressed in platelets, prior efforts to leverage this vulnerability in other cancers have been hampered by severe thrombocytopenia. To overcome this toxicity, we treated FLC models with DT2216, a proteolysis targeting chimera (PROTAC) that directs BCL-XL for degradation via the von Hippel-Lindau (VHL) E3 ligase, which is minimally expressed in platelets. The combination of irinotecan and DT2216 in vitro on cells directly acquired from patients or in vivo using several xenografts derived from patients with FLC demonstrated remarkable synergy and at clinically achievable doses not associated with significant thrombocytopenia. © 2022, Shebl et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
Keywords: liver cell carcinoma; carcinoma, hepatocellular; liver neoplasms; thrombocytopenia; liver tumor; piperazines; piperazine derivative; humans; human; dt2216
Journal Title: JCI Insight
Volume: 7
Issue: 17
ISSN: 2379-3708
Publisher: Amer Soc Clinical Investigation Inc  
Date Published: 2022-09-08
Start Page: e161820
Language: English
DOI: 10.1172/jci.insight.161820
PUBMED: 36073545
PROVIDER: scopus
PMCID: PMC9536265
DOI/URL:
Notes: Article -- Export Date: 3 October 2022 -- Source: Scopus
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  1. Michael Vincent Ortiz
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