Inhibition of CDK2, CDK4 and cyclin E and increased expression of p27Kip1 during treatment with interferon-α in carcinoid tumor cells

被引:0
|
作者
Zhou, Y [1 ]
Wang, S [1 ]
Gobl, A [1 ]
Oberg, K [1 ]
机构
[1] Univ Uppsala Hosp, Endocrine Oncol Unit, S-75185 Uppsala, Sweden
关键词
interferon alpha; carcinoid tumor; cell cycle; p27kip1; cyclin dependent kinase; immunodepletion;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IFN-alpha has presented antitumor effect in about 50% of carcinoid tumor patients, though the antitumor mechanism of IFN-alpha is still to be elucidated. In this study we demonstrated that IFN-alpha could result in accumulation of S-phase population and upregulation of cyclin-dependent kinase inhibitor (CKI), p27. Moreover, IFN-alpha inhibits DNA synthesis assessed by [H-3] thymidine incorporation and colony formation on soft agar. Immunodepletion of p27 increased CDK2- and cyclin E-associated kinase activities. These data suggest that IFN-a exerts its antiproliferative effects in the neuroendocrine differentiated cell lines by: 1) inhibition of DNA synthesis and colony formation, 2) upregulation on the mRNA and protein expressions of the CKI, p27.
引用
收藏
页码:207 / 215
页数:9
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