4.6 Review

PI3K pathway in prostate cancer: All resistant roads lead to PI3K

期刊

出版社

ELSEVIER
DOI: 10.1016/j.bbcan.2018.09.001

关键词

Cancer therapy; PI3K; Prostate cancer; Resistance

资金

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2017M3A9D8062960, 2018R1A4A1023822]
  2. Education and Research Encouragement Fund of Seoul National University Hospital
  3. Brain Korea 21 PLUS program
  4. National Research Foundation of Korea [2017M3A9D8062960, 2018R1A4A1023822] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The phosphoinositide 3-kinase (PI3K) pathway integrates multifarious environmental cues to regulate cell survival, growth, and metabolism. Hyperactivation of the PI3K pathway increases biological fitness by offering a high degree of adaptability to and resilience against diverse perturbations, thus conferring survival benefits on premalignant and transformed cells. In prostate cancer, the PI3K pathway is aberrantly activated by various genetic and epigenetic alterations and its hyperactivation is closely associated with a poor clinical outcome. In this review, we discuss the challenges encountered with clinically effective therapies targeting the PI3K pathway in prostate cancer, highlighting the clinical importance of combination therapies. In particular, we address how prostate cancer cells utilize the PI3K pathway for the development of resistance to a broad range of anticancer treatments. In addition, we describe the molecular mechanisms by which prostate cancer cells become resistant to PI3K pathway inhibitors. This review will be helpful in translating biological knowledge into therapeutic strategies for the treatment of prostate cancer and provide insight into overcoming therapeutic challenges associated with prostate cancer.

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

4.6
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