4.5 Review

Targeting GRP78 and antiestrogen resistance in breast cancer

期刊

FUTURE MEDICINAL CHEMISTRY
卷 5, 期 9, 页码 1047-1057

出版社

FUTURE SCI LTD
DOI: 10.4155/fmc.13.77

关键词

-

资金

  1. DOD Breast Cancer Research Program Postdoctoral Fellowship [BC112023]
  2. US Department of Health and Human Services [R01-CA131465, U54-CA149147]

向作者/读者索取更多资源

Breast cancer is the most prevalent cancer in women, with over 200,000 new cases diagnosed each year. Over 70% of breast cancers express the estrogen receptor-, and drugs targeting these receptors such as tamoxifen or Faslodex((R)) often fail to cure these patients. Many estrogen receptor-positive tumors lose drug sensitivity, making endocrine resistance a major clinical problem. Recently, investigation into the molecular mechanisms of endocrine resistance has highlighted a causative role of the unfolded protein response in antiestrogen resistance. In particular, the master regulator of the unfolded protein response, GRP78, was observed to be elevated in endocrine-resistant breast cancer and directly affected antiestrogen therapy responsiveness. GRP78 was found to impact many different cellular processes that may affect breast cancer survival. Recently, various compounds have been reported to affect GRP78 activity and it may be advantageous to combine these drugs with antiestrogens to overcome endocrine therapy resistance.

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