Literature DB >> 23150278

Tandem mass spectrometry for characterization of covalent adducts of DNA with anticancer therapeutics.

Catherine Silvestri1, Jennifer S Brodbelt.   

Abstract

The chemotherapeutic activities of many anticancer and antibacterial drugs arise from their interactions with nucleic acid substrates. Some of these ligands interact with DNA in a way that causes conformational changes or damage to the nucleic acid targets, ultimately altering recognition by key DNA-specific enzymes, interfering with DNA transcription or prohibiting replication, and terminating cell growth and proliferation. The design and synthesis of ligands that bind to nucleic acids remains a dynamic field in medicinal chemistry and pharmaceutical research. The quest for more selective and efficacious DNA-interactive antipan class="Disease">cancer chemotherapeutics has likewise catalyzed the need for sensitive analytical methods that can provide structural information about the nature of the resulting DNA adducts and provide insight into the mechanistic pathways of the DNA/drug interactions and the impact on the cellular processes in biological systems. This review focuses on the array of tandem mass spectrometric strategies developed and applied for characterization of covalent adducts formed between DNA and anticancer ligands.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 23150278      PMCID: PMC3578003          DOI: 10.1002/mas.21363

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  95 in total

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Journal:  Anal Chem       Date:  2003-11-15       Impact factor: 6.986

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Journal:  J Am Soc Mass Spectrom       Date:  2008-12-31       Impact factor: 3.262

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5.  Comprehensive exploration of the anticancer activities of procaine and its binding with calf thymus DNA: a multi spectroscopic and molecular modelling study.

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