Dual small-molecule targeting of procaspase-3 dramatically enhances zymogen activation and anticancer activity.

ABSTRACT: Combination anticancer therapy typically consists of drugs that target different biochemical pathways or those that act on different targets in the same pathway. Here we demonstrate a new concept in combination therapy, that of enzyme activation with two compounds that hit the same biological target, but through different mechanisms. Combinations of procaspase-3 activators PAC-1 and 1541B show considerable synergy in activating procaspase-3 in vitro, stimulate rapid and dramatic maturation of procaspase-3 in multiple cancer cell lines, and powerfully induce caspase-dependent apoptotic death to a degree well exceeding the additive effect. In addition, the combination of PAC-1 and 1541B effectively reduces tumor burden in a murine lymphoma model at dosages for which the compounds alone have

SUBMITTER: Botham RC 

PROVIDER: S-EPMC3954530 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature