Regulation of Actinomycin D induced upregulation of Mdm2 in H1299 cells

被引:4
作者
Li, Lianjie [1 ,2 ]
Cui, Di [1 ,2 ]
Zheng, Shijun J. [1 ,2 ]
Lou, Huiqiang [2 ,3 ]
Tang, Jun [1 ,2 ]
机构
[1] China Agr Univ, Coll Vet Med, Beijing 100193, Peoples R China
[2] China Agr Univ, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China
[3] China Agr Univ, Coll Biol Sci, Beijing 100193, Peoples R China
基金
中国国家自然科学基金;
关键词
Mdm2; Actinomycin D; Ribosomal stress; NEDDylation; ATM-DEPENDENT PHOSPHORYLATION; DNA-DAMAGE; P53; UBIQUITINATION; TUMOR-SUPPRESSOR; PROTEIN; DEGRADATION; INHIBITION; ACTIVATION; APOPTOSIS; PATHWAY;
D O I
10.1016/j.dnarep.2011.10.010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mdm2 is a critical negative regulator of the p53 tumor suppressor and also has many p53-independent functions. Deregulation of Mdm2 is closely associated with tumorigenesis. However, how Mdm2 is regulated in response to various stresses is not well understood. In this study, we found that Mdm2 was stabilized and upregulated upon Actinomycin D (ActD) treatment in the p53-deficient H1299 cell line. This Mdm2 upregulation was not dependent on the ribosomal protein L11, an essential player in ribosomal stress-induced p53 activation, but did require a NEDDylation-dependent mechanism. We further demonstrated that the ActD-induced Mdm2 stabilization may be modulated by the cell growth signaling, and that knockdown of Mdm2 enhanced ActD-induced cell death in H1299 cells. These results suggested a role of Mdm2 in the ribosomal stress response in the p53 deficient cells, which could be exploited in therapeutic use for treating cancers harboring p53 mutations. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 119
页数:8
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