Reactivation of mutant p53 and induction of apoptosis in human tumor cells by maleimide analogs

被引:195
作者
Bykov, VJN
Issaeva, N
Zache, N
Shilov, A
Hultcrantz, M
Bergman, J
Selivanova, G [1 ]
Wiman, KG
机构
[1] Karolinska Univ Hosp, Dept Oncol Pathol, Ctr Canc, Stockholm, Sweden
[2] Karolinska Inst, MTC, SE-17177 Stockholm, Sweden
[3] Inst Cytol & Genet, Novosibirsk 630090, Russia
[4] Karolinska Inst, Dept Biosci, SE-14157 Huddinge, Sweden
关键词
D O I
10.1074/jbc.M501664200
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
Reactivation of mutant p53 is likely to provide important benefits for treatment of chemotherapy- and radio-therapy-resistant tumors. We demonstrate here that the maleimide-derived molecule MIRA-1 can reactivate DNA binding and preserve the active conformation of mutant p53 protein in vitro and restore transcriptional transactivation to mutant p53 in living cells. MIRA-1 induced mutant p53-dependent cell death in different human tumor cells carrying tetracycline-regulated mutant p53. The structural analog MIRA-3 showed antitumor activity in vivo against human mutant p53-carrying tumor xenografts in SCID mice. The MIRA scaffold is a novel lead for the development of anticancer drugs specifically targeting mutant p53.
引用
收藏
页码:30384 / 30391
页数:8
相关论文
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