The BH3 mimetic compound, ABT-737, synergizes with a range of cytotoxic chemotherapy agents in chronic lymphocytic leukemia

Mason, KD; Khaw, SL; Rayeroux, KC; Chew, E; Lee, EF; Fairlie, WD; Grigg, AP; Seymour, JF; Szer, J; Huang, DCS; Roberts, AW

Author(s): Mason, KD; Khaw, SL; Rayeroux, KC; Chew, E; Lee, EF; Fairlie, WD; Grigg, AP; Seymour, JF; Szer, J; Huang, DCS; Roberts, AW;
Details: Publication Year 2009-11,Volume 23,Issue #11,Page 2034-2041
Journal Title: LEUKEMIA
Publication Type: Journal Article
Abstract: As chronic lymphocytic leukemia (CLL) is characterized by overexpression of pro-survival BCL2, compounds that mimic its physiological antagonists, the BH3-only proteins, may have a role in treatment of this disease. ABT-737 is a BH3 mimetic compound that selectively targets BCL2 and BCLX(L). In the present work, we report that ABT-737 is highly effective (LC(50) < 50 nM) as a single agent against most (21/30) primary CLL samples, but that a sizable minority is relatively insensitive. In vitro sensitivity to ABT-737 could not be simply predicted by the patients' clinical features, including response to prior therapy or known prognostic markers (CD38 expression, 17p deletion), or the relative expression of BCL2 family proteins (BCL2, MCL1, BAX, BIM). Strikingly, co-incubation with cytotoxic agents (dexamethasone, etoposide, fludarabine, doxorubicin) sensitized most CLL samples to ABT-737, but this could not be predicted by responses to either ABT-737 or the cytotoxic agent alone. Of 17 samples least sensitive to ABT-737, 13 were sensitized by co-treatment with at least one cytotoxic agent. These data indicate that combination of ABT-737 with a second anti-leukemic agent would improve response rates and suggest a potential role for combination therapies that include BH3 mimetics for the treatment of this disease. Leukemia (2009) 23, 2034-2041; doi: 10.1038/leu.2009.151; published online 30 July 2009
Publisher: NATURE PUBLISHING GROUP
Keywords: BCL-W; ANTAGONIST ABT-737; BH3-ONLY PROTEINS; ZAP-70 EXPRESSION; IN-VITRO; APOPTOSIS; CELLS; SENSITIVITY; FLUDARABINE; MECHANISMS
Publisher's Version: https://doi.org/10.1038/leu.2009.151
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Creation Date: 2009-11-01 12:00:00