Inhibiting DNA Polymerases as a Therapeutic Intervention against Cancer

被引:51
作者
Berdis, Anthony J. [1 ,2 ,3 ]
机构
[1] Cleveland State Univ, Dept Chem, Cleveland, OH 44115 USA
[2] Cleveland State Univ, Ctr Gene Regulat Hlth & Dis, Cleveland, OH 44115 USA
[3] Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
关键词
DNA polymerases; chemotherapy; nucleoside analogs; DNA damaging agents; cancer; LESION BYPASS; TRANSFERASE EXPRESSION; THYMINE DIMER; MINOR-GROOVE; PHASE-I; REPLICATION; GEMCITABINE; 9-BETA-D-ARABINOFURANOSYL-2-FLUOROADENINE; CHLORAMBUCIL; FLUDARABINE;
D O I
10.3389/fmolb.2017.00078
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
Inhibiting DNA synthesis is an important therapeutic strategy that is widely used to treat a number of hyperproliferative diseases including viral infections, autoimmune disorders, and cancer. This chapter describes two major categories of therapeutic agents used to inhibit DNA synthesis. The first category includes purine and pyrmidine nucleoside analogs that directly inhibit DNA polymerase activity. The second category includes DNA damaging agents including cisplatin and chlorambucil that modify the composition and structure of the nucleic acid substrate to indirectly inhibit DNA synthesis. Special emphasis is placed on describing the molecular mechanisms of these inhibitory effects against chromosomal and mitochondrial DNA polymerases. Discussions are also provided on the mechanisms associated with resistance to these therapeutic agents. A primary focus is toward understanding the roles of specialized DNA polymerases that by-pass DNA lesions produced by DNA damaging agents. Finally, a section is provided that describes emerging areas in developing new therapeutic strategies targeting specialized DNA polymerases.
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页数:12
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