IL-2 signals through Sgkl and inhibits proliferation and apoptosis in kidney cancer cells

被引:54
作者
Amato, Rosario
Menniti, Miranda
Agosti, Valter
Boito, Rosalia
Costa, Nicola
Bond, Heather M.
Barbieri, Vito
Tagliaferri, Pierosandro
Venuta, Salvatore
Perrotti, Nicola
机构
[1] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med G Salvatore, I-88100 Catanzaro, Italy
[2] Magna Graecia Univ Catanzaro, Dept Pharmacobiol, Catanzaro, Italy
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2007年 / 85卷 / 07期
关键词
interleukin-2; Sgk1 kidney cancer cells; cell proliferation; apoptosis;
D O I
10.1007/s00109-007-0205-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The interleukin-2 is a cytokine that is essential for lymphocytic survival and function. Ectopic expression of the IL-2 receptor in epithelial tissues has been reported previously, although the functional significance of this expression is still being investigated. We provided novel structural and functional information on the expression of the IL-2 receptor in kidney cancer cells and in other normal and neoplastic human epithelial tissues. In A-498 kidney cancer cells, we showed that IL-2 binding to its own receptor triggers a signal transduction pathway leading to the inhibition of proliferation and apoptosis. We found that the inhibition of proliferation is associated with Erk1/2 dephosphorylation, whereas the survival signals appear to be mediated by Sgk1 activation. This investigation focuses on the IL-2 induced regulation of Sgk1 and describes a role of the IL-2 receptor and Sgk1 in the regulation of epithelial tumor cell death and survival.
引用
收藏
页码:707 / 721
页数:15
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