4.7 Article

Antitumor activity of novel fluoro-substituted (-)-epigallocatechin-3-gallate analogs

期刊

CANCER LETTERS
卷 292, 期 1, 页码 48-53

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2009.11.006

关键词

Breast cancer; Proteasome inhibitor; Drug discovery; Cancer prevention; Tea polyphenol

类别

资金

  1. Karmanos Cancer Institute of Wayne State University
  2. National Cancer Institute/NIH [1R01CA120009, 3R01CA120009-04S1]
  3. National Cancer Institute/NIH Cancer Center
  4. NATIONAL CANCER INSTITUTE [R01CA120009] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Epidemiological studies support the cancer-preventive effects of green tea and its main constituent (-)-epigallocatechin gallate [(-)-EGCG], however, (-)-EGCG is unstable under physiological conditions. Here we report that two novel fluoro-substituted (-)-EGCG analogs inhibited tumor growth with similar potency to that of Pro-EGCG (1) which has improved potency over parental compound (-)-EGCG in human breast cancer MDA-MB-231 xenografts. MDA-MB-231 tumors treated with each fluoro-substituted (-)-EGCG analog showed proteasome inhibition and apoptotic cell death, suggesting that the proteasome might be one of the cellular targets of fluoro-(-)-EGCGs and that proteasome inhibition is partially responsible for the observed antitumor activity. (C) 2009 Elsevier Ireland Ltd. 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

4.7
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