Sox-4 is a positive regulator of Hep3B and HepG2 cells' apoptosis induced by prostaglandin (PG)A2 and Δ12-PGJ2

被引:41
作者
Ahn, SG
Kim, HS
Jeong, SW
Kim, BE
Rhim, H
Shim, JY
Kim, JW
Lee, JH
Kim, IK
机构
[1] Catholic Univ Korea, Coll Med, Dept Biochem, Socho Gu, Seoul 137701, South Korea
[2] Catholic Univ Korea, Coll Med, Res Inst Mol Genet, Socho Gu, Seoul 137701, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Anesthesiol, Socho Gu, Seoul 137701, South Korea
关键词
Sox-4; PGA(2); Delta(12)-PGJ(2); apoptosis;
D O I
10.1038/emm.2002.34
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
We reported earlier that expression of Sox-4 was found to be elevated during prostaglandin (PG) A2 and Delta(12)-PGJ(2) induced apoptosis in human hepatocarcinoma Hep3B cells. In this study, the role of Sox-4 was examined using human Hep3B and HepG2 cell lines. Sox-4 induction by several apoptotic inducer such as A23187 (Ca2+ ionophore) and etoposide (topoisomerase II inhibitor) and Sox-4 transfection into the cells were able to induce apoptosis as observed by the cellular DNA fragmentation. Antisense oligonucleotide of Sox-4 inhibited the induction of Sox-4 expression and blocked the formation of DNA fragmentation by PGA(2) and (12)-PGJ(2) in Hep3B and HepG2 cells. Sox-4-induced apoptosis was accompanied with caspase-1 activation indicating that caspase cascade was involved in this apoptotic pathway. These results indicate that Sox-4 is involved in Hep3B and HepG2 cells apoptosis as an important apoptotic mediator.
引用
收藏
页码:243 / 249
页数:7
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