多胺
PI3K/AKT/mTOR通路
癌症
癌变
Wnt信号通路
mTORC1型
癌症研究
生物
精胺
化学
生物信息学
生物化学
信号转导
遗传学
酶
作者
Robert A. Casero,Tracy Murray Stewart,Anthony E. Pegg
出处
期刊:Nature Reviews Cancer
[Springer Nature]
日期:2018-09-04
卷期号:18 (11): 681-695
被引量:558
标识
DOI:10.1038/s41568-018-0050-3
摘要
Advances in our understanding of the metabolism and molecular functions of polyamines and their alterations in cancer have led to resurgence in the interest of targeting polyamine metabolism as an anticancer strategy. Increasing knowledge of the interplay between polyamine metabolism and other cancer-driving pathways, including the PTEN–PI3K–mTOR complex 1 (mTORC1), WNT signalling and RAS pathways, suggests potential combination therapies that will have considerable clinical promise. Additionally, an expanding number of promising clinical trials with agents targeting polyamines for both therapy and prevention are ongoing. New insights into molecular mechanisms linking dysregulated polyamine catabolism and carcinogenesis suggest additional strategies that can be used for cancer prevention in at-risk individuals. In addition, polyamine blocking therapy, a strategy that combines the inhibition of polyamine biosynthesis with the simultaneous blockade of polyamine transport, can be more effective than therapies based on polyamine depletion alone and may involve an antitumour immune response. These findings open up new avenues of research into exploiting aberrant polyamine metabolism for anticancer therapy. This Review discusses new insights into molecular mechanisms that link the dysregulation of polyamine metabolism with carcinogenesis and strategies for targeting this pathway for cancer therapy.
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