Expression of the RAI gene is conducive to apoptosis:: Studies of induction and interference

被引:22
作者
Laska, Magdalena J.
Strandbygard, Dorthe
Kjeldgaard, Anette
Mains, Mette
Corydon, Thomas J.
Memon, Ashfaque A.
Sorensen, Boe S.
Vogel, Ulla
Jensen, Uffe B.
Nexo, Bjorn A.
机构
[1] Univ Aarhus, Inst Human Genet, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Clin Biochem, DK-8000 Aarhus, Denmark
[3] Natl Inst Occupat Hlth, Copenhagen, Denmark
[4] Aarhus Univ Hosp, Dept Clin Genet, DK-8000 Aarhus, Denmark
关键词
apoptosis; lymphocytes; gene RAI; NF-kappa B; etoposide VP-16;
D O I
10.1016/j.yexcr.2007.05.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The RAI gene is also known as iASPP and PPP1R13L. Recent investigations have shown that the region encompassing RAI is important for the development of cancer in young and middle-aged persons. it has been speculated that the RAI product induces apoptosis by blocking NF-KB or inhibits apoptosis by blocking p53. Either way the gene could influence the survival of precancerous lesions. Here we report that the expression of RAI mRNA was increased in non-transformed lymphocytes and fibroblasts induced to undergo apoptosis by various means, such as treatment with etoposide, calcium ions, or interleukin-2 and/or serum deprivation. Treatment with etoposide increased the content of RAI protein, too, and caused it to translocate to the nucleus. Inhibition of RAI expression in lymphocytes and fibroblasts with siRNA reduced apoptosis, but treatment with the NF-KB-inhibiting substance sulfasalazine relieved this dependence. in the transformed cell line HEK-293 the association between RAI induction and apoptosis seemed broken. Thus, we hypothesize that RAI induction is necessary but not sufficient for apoptosis induction in non-transformed cells. Our results could be explained by a NF-KB mediated mechanism. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:2611 / 2621
页数:11
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