Checkpoint kinase 1 is cleaved in a caspase-dependent pathway during genotoxic stress-induced apoptosis.

Abstract:

:Checkpoint kinase 1 (Chk1) plays important roles in genotoxic stress-induced cell cycle checkpoint and in normal cell cycle progression. Here, we show that Chk1 is cleaved in the treatment of apoptotic dose of etoposide (ETP) or cisplatin (CIS) but not of viable dose in HeLa S3 cells. The cleavage of Chk1 was completely inhibited by an irreversible and cell-permeable pan-caspase inhibitor, N-benzyloxycarbonyl-Val-Ala-Asp (OMe) fluoromethylketone (z-VAD-fmk). These results identify Chk1 as a novel substrate that is cleaved by a caspase-dependent manner during genotoxic stress-induced apoptosis. Our data may also indicate the existence of a novel Chk1-regulated apoptotic pathway.

journal_name

Biol Pharm Bull

authors

Okita N,Kudo Y,Tanuma S

doi

10.1248/bpb.30.359

subject

Has Abstract

pub_date

2007-02-01 00:00:00

pages

359-62

issue

2

eissn

0918-6158

issn

1347-5215

pii

JST.JSTAGE/bpb/30.359

journal_volume

30

pub_type

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