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Chromatin as a Target for the DNA-Binding Anticancer Drugs.

Authors :
Harris, J. R.
Biswas, B. B.
Quinn, P.
Kundu, Tapas K.
Bittman, R.
Dasgupta, D.
Engelhardt, H.
Flohe, L.
Herrmann, H.
Holzenburg, A.
Nasheuer, H-P.
Rottem, S.
Wyss, M.
Zwickl, P.
Majumder, Parijat
Pradhan, Suman K.
Devi, Pukhrambam Grihanjali
Pal, Sudipta
Dasgupta, Dipak
Source :
Chromatin & Disease; 2007, p145-192, 48p
Publication Year :
2007

Abstract

Chemotherapy has been a major approach to treat cancer. Both constituents of chromatin, chromosomal DNA and the associated chromosomal histone proteins are the molecular targets of the anticancer drugs. Small DNA binding ligands, which inhibit enzymatic processes with DNA substrate, are well known in cancer chemotherapy. These drugs inhibit the polymerase and topoisomerase activity. With the advent in the knowledge of chromatin chemistry and biology, attempts have shifted from studies of the structural basis of the association of these drugs or small ligands (with the potential of drugs) with DNA to their association with chromatin and nucleosome. These drugs often inhibit the expression of specific genes leading to a series of biochemical events. An overview will be given about the latest understanding of the molecular basis of their action. We shall restrict to those drugs, synthetic or natural, whose prime cellular targets are so far known to be chromosomal DNA [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISBNs :
9781402054655
Database :
Supplemental Index
Journal :
Chromatin & Disease
Publication Type :
Book
Accession number :
33257234
Full Text :
https://doi.org/10.1007/1-4020-5466-1_8