Tributyltin induces a G2/M cell cycle arrest in human amniotic cells via PP2A inhibition-mediated inactivation of the ERK1/2 cascades

被引:5
|
作者
Zhang, Yali [1 ,3 ]
Guo, Zonglou [2 ]
Xu, Lihong [3 ]
机构
[1] Nantong Univ, Sch Med, Dept Biochem, Nantong 226001, Peoples R China
[2] Zhejiang Univ, Dept Biosyst Engn, Coll Biosyst Engn & Food Sci, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Dept Biochem & Genet, Hangzhou 310058, Zhejiang, Peoples R China
关键词
Tributyltin; Cell cycle arrest; PP2A; Cdc25C; Cdc2; ERK1/2; cascades; PROTEIN-KINASE PATHWAY; G(2)/M TRANSITION; INDUCED APOPTOSIS; PHOSPHATASE; 2A; MAP KINASES; MYC; ACTIVATION; MECHANISMS; EXPRESSION; REGULATOR;
D O I
10.1016/j.etap.2014.02.009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The molecular mechanisms underlying the cell cycle alterations induced by tributyltin (TBT), a highly toxic environmental contaminant, remain elusive. In this study, cell cycle progression and some key regulators in G2/M phase were investigated in human amniotic cells treated with TBT. Furthermore, protein phosphatase (PP) 2A and the ERK cascades were examined. The results showed that TBT caused a G2/M cell cycle arrest that was accompanied by a decrease in the total cdc25C protein level and an increase in the p-cdc2 level in the nucleus. TBT caused a decrease in PP2A activity and inhibited the ERK cascade by inactivating Raf-1, resulting in the dephosphorylation of MEK1/2, ERK1/2, and c-Myc. Taken together, TBT leads to a G2/M cell cycle arrest in FL cells, an increase in p-cdc2 and a decrease in the levels of total cdc25C protein, which may be caused by the PP2A inhibition-mediated inactivation of the ERK1/2 cascades. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:812 / 818
页数:7
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