4.7 Review

Discovery of selective phosphatidylinositol 3-kinase inhibitors to treat hematological malignancies

期刊

DRUG DISCOVERY TODAY
卷 20, 期 8, 页码 988-994

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.drudis.2015.03.009

关键词

-

资金

  1. Natural Science Foundation of China [81272632, 81320108023]
  2. Natural Science Foundation of Jiangsu Province [BE2014630]
  3. National Basic Research Program of China [2011CB933501]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  5. Jiangsu Key Laboratory for Translational Research and Therapeutics of Neuro-Psycho-Diseases [BK2013003]

向作者/读者索取更多资源

The phosphatidylinositol 3-kinase (PI3K) signaling pathway is associated with chemoresistance and poor prognosis of many cancers, including hematological malignancies (HM), such as leukemia, lymphomas, and multiple myeloma (MM). Targeting PI3K is emerging as a promising strategy in the treatment of these blood cancers. Recent approval of idelalisib, a specific inhibitor of PI3K delta, for the treatment of several types of HM, is likely to attract more interest in search for novel PI3K inhibitors. Here, we discuss classic and cutting-edge techniques and strategies to identify PI3K inhibitors for the treatment of HM. Each technique has its own strengths and limitations, and their combined application will accelerate the drug discovery process with fewer associated costs.

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