Blockage of BCL-XL overcomes venetoclax resistance across BCL2+lymphoid malignancies irrespective of BIM status

Warning

This publication doesn't include Faculty of Economics and Administration. It includes Central European Institute of Technology. Official publication website can be found on muni.cz.

Authors	DOLNIKOVA Alexandra KAZANTSEV Dmitry KLANOVA Magdalena POKORNA Eva SOVILJ Dana KELEMEN Cristina Daniela TUSKOVA Liliana HOFERKOVÁ Eva MRÁZ Marek HELMAN Karel CURIK Nikola MACHOVA POLAKOVA Katerina ANDERA Ladislav TRNENY Marek KLENER Pavel
Year of publication	2024
Type	Article in Periodical
Magazine / Source	Blood advances
MU Faculty or unit	Central European Institute of Technology
Citation
Web	https://ashpublications.org/bloodadvances/article/8/13/3532/516030/Blockage-of-BCL-XL-overcomes-venetoclax-resistance
Doi	http://dx.doi.org/10.1182/bloodadvances.2024012906
Attached files	Blockage_of_BCL-XL_overcomes_venetoclax_resistance_across_BCL2__lymphoid_malignancies_irrespective_of_BIM_status.pdf
Description	Venetoclax (VEN), a B-cell lymphoma 2 (BCL2) inhibitor, has a promising single-agent activity in mantle cell lymphoma (MCL), acute lymphoblastic leukemia (ALL), and large BCLs, but remissions were generally short, which call for rational drug combinations. Using a panel of 21 lymphoma and leukemia cell lines and 28 primary samples, we demonstrated strong synergy between VEN and A1155463, a BCL-XL inhibitor. Immunoprecipitation experiments and studies on clones with knockout of expression or transgenic expression of BCL-XL confirmed its key role in mediating inherent and acquired VEN resistance. Of note, the VEN and A1155463 combination was synthetically lethal even in the cell lines with lack of expression of the proapoptotic BCL2L11/BIM and in the derived clones with genetic knockout of BCL2L11/BIM. This is clinically important because BCL2L11/BIM deletion, downregulation, or sequestration results in VEN resistance. Immunoprecipitation experiments further suggested that the proapoptotic effector BAX belongs to principal mediators of the VEN and A1155463 mode of action in the BIM-deficient cells. Lastly, the efficacy of the new proapoptotic combination was confirmed in vivo on a panel of 9 patient-derived lymphoma xenografts models including MCL (n = 3), B-ALL (n = 2), T-ALL (n = 1), and diffuse large BCL (n = 3). Because continuous inhibition of BCL-XL causes thrombocytopenia, we proposed and tested an interrupted 4 days on/3 days off treatment regimen, which retained the desired antitumor synergy with manageable platelet toxicity. The proposed VEN and A1155463 combination represents an innovative chemotherapy-free regimen with significant preclinical activity across diverse BCL2+ hematologic malignancies irrespective of the BCL2L11/BIM status.
Related projects:	National institute for cancer research Development of models for the studies of microenvironment and therapeutic resistance in B cell malignancies