Literature DB >> 8960461

Analysis of eukaryotic DNA topoisomerases and topoisomerase-directed drug effects.

F Boege1.   

Abstract

DNA topoisomerases are enzymes which control DNA topology by cleaving and rejoining DNA strands and passing other DNA strands through the transient gaps. Consequently these enzymes play a crucial role in the regulation of the physiological function of the genome. Beyond their normal functions, topoisomerases are important cellular targets in the treatment of human cancers. Some of the most powerful anti-cancer drugs used clinically stabilize the catalytic topoisomerase-DNA intermediates and, thus, cause DNA disorders that will induce apoptosis in proliferating cells. This review summarizes current protocols for measuring the catalytic activity of topoisomerases and for monitoring the molecular effects of topoisomerase-directed antitumour drugs in living cells and in cell-free assays. Furthermore, preanalytical factors are discussed, such as enzyme stability, methods for extracting DNA topoisomerases from cells, and protocols for separating subtypes and isoforms of these enzymes.

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Year:  1996        PMID: 8960461

Source DB:  PubMed          Journal:  Eur J Clin Chem Clin Biochem        ISSN: 0939-4974


  5 in total

1.  Parameiosis in Aspergillus nidulans in response to doxorubicin.

Authors:  T C A Becker; M A A De Castro-Prado
Journal:  Folia Microbiol (Praha)       Date:  2004       Impact factor: 2.099

2.  The extended-MDR phenotype.

Authors:  R Davey; M Davey
Journal:  Cytotechnology       Date:  1998-09       Impact factor: 2.058

3.  Design and development of topoisomerase inhibitors using molecular modelling studies.

Authors:  Muthu K Kathiravan; Madhavi M Khilare; Aparna S Chothe; Madhuri A Nagras
Journal:  J Chem Biol       Date:  2012-09-29

4.  Functional interaction between human topoisomerase IIalpha and retinoblastoma protein.

Authors:  U G Bhat; P Raychaudhuri; W T Beck
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

5.  Lycobetaine acts as a selective topoisomerase II beta poison and inhibits the growth of human tumour cells.

Authors:  H U Barthelmes; E Niederberger; T Roth; K Schulte; W C Tang; F Boege; H H Fiebig; G Eisenbrand; D Marko
Journal:  Br J Cancer       Date:  2001-11-16       Impact factor: 7.640

  5 in total

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