4.5 Article

Uncoupling JAK3 activation induces apoptosis in human lymphoid cancer cells via regulating critical survival pathways

期刊

FEBS LETTERS
卷 584, 期 8, 页码 1515-1520

出版社

WILEY
DOI: 10.1016/j.febslet.2010.02.071

关键词

Janus kinase; Apoptosis; Lymphoid cancer; Microarray; Gene expression

资金

  1. Texas Ignition Fund
  2. Lizanell and Colbert Coldwell Foundation
  3. ZSN [S06 GM008012-37]
  4. National Center for Research Resources (NCRR) [5G12RR008124]

向作者/读者索取更多资源

In the current work, we report that specific inhibition of Janus tyrosine kinase (JAK3) via NC1153 induces apoptosis of certain leukemia/lymphoma cell lines. Affymetrix microarray profiling following NC1153 treatment unveiled JAK3 dependent survival modulating pathways (p53, TGF-beta, TNFR and ER stress) in Kit225 cells. IL-2 responsive NC1153 target genes were regulated in human JAK3 positive, but not in JAK3 negative lymphoid tumor cells. Moreover, primary lymphoma samples revealed that a number of these genes were reciprocally regulated during disease progression and JAK3 inhibition suggesting that downstream targets of JAK3 could be exploited in the development of novel cancer treatment regimes. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据