Understanding different functions of mammalian AP endonuclease (APE1) as a promising tool for cancer treatment

被引:121
作者
Tell, Gianluca [1 ]
Fantini, Damiano [1 ]
Quadrifoglio, Franco [1 ]
机构
[1] Univ Udine, Dept Biomed Sci & Technol, I-33100 Udine, Italy
关键词
Base excision repair; Oxidative stress; Redox signalling; Nucleolus; Cancer; BASE EXCISION-REPAIR; HUMAN APURINIC/APYRIMIDINIC ENDONUCLEASE; NF-KAPPA-B; HUMAN APURINIC ENDONUCLEASE; DNA-POLYMERASE-BETA; REDOX FACTOR-I; NEGATIVE GENE-REGULATION; OXIDATIVE STRESS; TRANSCRIPTION FACTOR; MESSENGER-RNA;
D O I
10.1007/s00018-010-0486-4
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
The apurinic endonuclease 1/redox factor-1 (APE1) has a crucial function in DNA repair and in redox signaling in mammals, and recent studies identify it as an excellent target for sensitizing tumor cells to chemotherapy. APE1 is an essential enzyme in the base excision repair pathway of DNA lesions caused by oxidation and alkylation. As importantly, APE1 also functions as a redox agent maintaining transcription factors involved in cancer promotion and progression in an active reduced state. Very recently, a new unsuspected function of APE1 in RNA metabolism was discovered, opening new perspectives for this multifunctional protein. These observations underline the necessity to understand the molecular mechanisms responsible for fine-tuning its different biological functions. This survey intends to give an overview of the multifunctional roles of APE1 and their regulation in the context of considering this protein a promising tool for anticancer therapy.
引用
收藏
页码:3589 / 3608
页数:20
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