Discovery of Small Molecules that Target Autophagy for Cancer Treatment

被引:13
作者
Wu, L. [1 ]
Yan, B. [1 ,2 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[2] St Jude Childrens Hosp, Dept Chem Biol & Therapeut, Memphis, TN 38105 USA
基金
中国国家自然科学基金;
关键词
Autophagy; autophagic cell death; drug discovery; autophagy regulators; cancer treatment; MALIGNANT GLIOMA-CELLS; PROTEIN-KINASE; DRUG-RESISTANCE; SELF-DIGESTION; DEATH; APOPTOSIS; INHIBITION; INDUCTION; DISEASE; BECLIN-1;
D O I
10.2174/092986711795496773
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy is a self-renewal process in cells by recycling redundant materials through lysosomal machinery. The basal level of autophagy in eukaryotic cells plays a "housekeeping" role by degrading redundant cellular materials and providing nutrients and energy. However acute and sustained autophagy may cause autophagic cell death. These two features of autophagy are consistent with its complex roles in both oncogenesis and cancer development. Many small molecule autophagy regulators are developed to turn autophagy on/off for therapeutic purpose. The roles of chemotherapeutic agents in regulating autophagy and facilitating cancer treatment can be classified into three categories: direct autophagy enhancers, indirect autophagy enhancers and autophagy inhibitors. The representative autophagy regulators and their roles in cancer treatment were reviewed.
引用
收藏
页码:1866 / 1873
页数:8
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