DNA Polymerases as Therapeutic Targets

Anthony J. Berdis*
Department of Pharmacology, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, Ohio 44106
Biochemistry, 2008, 47 (32), pp 8253–8260
DOI: 10.1021/bi801179f
Publication Date (Web): July 19, 2008
Copyright © 2008 American Chemical Society

This work was supported by funding from the National Institutes of Health (Grant CA118408).

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* To whom correspondence should be addressed. Telephone: (216) 368-4723. Fax: (216) 368-1300. E-mail: ajb15@case.edu.

Abstract

Abstract Image

Numerous pathological states, including cancer, autoimmune diseases, and viral/bacterial infections, are often attributed to uncontrollable DNA replication. Inhibiting this essential biological process provides an obvious therapeutic target against these diseases. A logical target is the DNA polymerase, the enzyme responsible for catalyzing the addition of mononucleotides to a growing polymer using a DNA or RNA template as a guide for directing each incorporation event. This review provides a summary of therapeutic agents that target polymerase activity. A discussion of the biological function and mechanism of polymerases is first provided to illustrate the strategy for therapeutic intervention as well as the rational design of various nucleoside analogues that inhibit various polymerases associated with viral infections and cancer. The development of nucleoside and non-nucleoside inhibitors as antiviral agents is discussed with particular emphasis on their mechanism of action, structure−activity relationships, toxicity, and mechanism of resistance. In addition, commonly used anticancer agents are described to illustrate the similarities and differences associated with various nucleoside analogues as therapeutic agents. Finally, new therapeutic approaches that include the inhibition of selective polymerases involved in DNA repair and/or translesion DNA synthesis as anticancer agents are discussed.

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History

  • Published In Issue August 12, 2008
  • Article ASAPJuly 19, 2008
  • Received: June 24, 2008

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