4.0 Article

Panobinostat.: Histone deacetylase (HDAC) inhibitor, apoptosis inducer, oncolytic

期刊

DRUGS OF THE FUTURE
卷 32, 期 4, 页码 315-322

出版社

PROUS SCIENCE, SAU-THOMSON REUTERS
DOI: 10.1358/dof.2007.032.04.1094476

关键词

-

向作者/读者索取更多资源

Panobinostat (LBH-589) is a member of the hydroxamic acid group of histone deacetylase (HDAC) inhibitors that have been shown to impede multiple pathways implicated in cancer and reverse epigenetic events associated with cancer, thereby reducing survival and inducing apoptosis in cancer cells. Panobinostat is being investigated in various hematological malignancies, including chronic myelogenous leukemia (CML) and multiple myeloma, and in solid tumors. Preclinical data indicate efficacy against drug-resistant cancer cells, both as a single agent and in combination with other therapies. A phase I clinical study has demonstrated activity in treatment-experienced patients with cutaneous T-cell lymphoma (CTCL) and phase II/III trials for this condition, and other hematological malignancies are ongoing.

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

4.0
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