Research Publications

Back

Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy


Leverson, JD; Phillips, DC; Mitten, MJ; Boghaert, ER; Diaz, D; Tahir, SK; Belmont, LD; Nimmer, P; Xiao, Y; Ma, XM; Lowes, KN; Kovar, P; Chen, J; Jin, S; SMITH, M; Xue, J; Zhang, H; Oleksijew, A; Magoc, TJ; Vaidya, KS; Albert, DH; Tarrant, JM; La, N; Wang, L; Tao, ZF; Wendt, MD; Sampath, D; Rosenberg, SH; Tse, C; SHuang DC; Fairbrother, WJ; Elmore, SW; Souers, AJ
2015-03-18
Sci Transl Med
Journal Article
7
279
279ra40
The BCL-2/BCL-XL/BCL-W inhibitor ABT-263 (navitoclax) has shown promising clinical activity in lymphoid malignancies such as chronic lymphocytic leukemia. However, its efficacy in these settings is limited by thrombocytopenia caused by BCL-XL inhibition. This prompted the generation of the BCL-2-selective inhibitor venetoclax (ABT-199/GDC-0199), which demonstrates robust activity in these cancers but spares platelets. Navitoclax has also been shown to enhance the efficacy of docetaxel in preclinical models of solid tumors, but clinical use of this combination has been limited by neutropenia. We used venetoclax and the BCL-XL-selective inhibitors A-1155463 and A-1331852 to assess the relative contributions of inhibiting BCL-2 or BCL-XL to the efficacy and toxicity of the navitoclax-docetaxel combination. Selective BCL-2 inhibition suppressed granulopoiesis in vitro and in vivo, potentially accounting for the exacerbated neutropenia observed when navitoclax was combined with docetaxel clinically. By contrast, selectively inhibiting BCL-XL did not suppress granulopoiesis but was highly efficacious in combination with docetaxel when tested against a range of solid tumors. Therefore, BCL-XL-selective inhibitors have the potential to enhance the efficacy of docetaxel in solid tumors and avoid the exacerbation of neutropenia observed with navitoclax. These studies demonstrate the translational utility of this toolkit of selective BCL-2 family inhibitors and highlight their potential as improved cancer therapeutics.
AAAS
Cancer and Haematology ; Systems Biology and Personalised Medicine
10.1126/scitranslmed.aaa4642
25787766
Refer to article for additional funding acknowledgements
Refer to copyright notice on published article.

Back
Creation Date 2015-05-20 10:11:24 Last Modified 2015-05-20 01:11:37