Procaspase-3 Overexpression in Cancer: A Paradoxical Observation with Therapeutic Potential

被引:82
作者
Boudreau, Matthew W.
Peh, Jessie
Hergenrother, Paul J. [1 ]
机构
[1] Univ Illinois, Dept Chem, 1209 W Calif St, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
ACTIVATING COMPOUND B-PAC-1; SMALL-MOLECULE ACTIVATOR; SQUAMOUS-CELL CARCINOMA; CASPASE-3; EXPRESSION; IN-VITRO; BREAST-CANCER; IMMUNOHISTOCHEMICAL EXPRESSION; BIOLOGICAL EVALUATION; PROGNOSTIC MARKERS; APOPTOSIS PROTEINS;
D O I
10.1021/acschembio.9b00338
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many anticancer strategies rely on the promotion of apoptosis in cancer cells as a means to shrink tumors. Crucial for apoptotic function are executioner caspases, most notably caspase-3, that proteolyze a variety of proteins, inducing cell death. Paradoxically, overexpression of procaspase-3 (PC-3), the low-activity zymogen precursor to caspase-3, has been reported in a variety of cancer types. Until recently, this counterintuitive overexpression of a pro-apoptotic protein in cancer has been puzzling. Recent studies suggest subapoptotic caspase-3 activity may promote oncogenic transformation, a possible explanation for the enigmatic overexpression of PC-3. Herein, the overexpression of PC-3 in cancer and its mechanistic basis is reviewed; collectively, the data suggest the potential for exploitation of PC-3 overexpression with PC-3 activators as a targeted anticancer strategy.
引用
收藏
页码:2335 / 2348
页数:14
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