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DNA-Targeted Inhibition of MGMT.

Authors :
Marsoner T
Schmidt OP
Triemer T
Luedtke NW
Source :
Chembiochem : a European journal of chemical biology [Chembiochem] 2017 May 18; Vol. 18 (10), pp. 894-898. Date of Electronic Publication: 2017 Apr 07.
Publication Year :
2017

Abstract

The cationic porphyrin 5,10,15,20-tetrakis (diisopropyl-guanidine)-21H,23H-porphine (DIGPor) selectively binds to DNA containing O <superscript>6</superscript> -methylguanine (O <superscript>6</superscript> -MeG) and inhibits the DNA repair enzyme O <superscript>6</superscript> -methylguanine-DNA methyltransferase (MGMT). The O <superscript>6</superscript> -MeG selectivity and MGMT inhibitory activity of DIGPor were improved by incorporating Zn <superscript>II</superscript> into the porphyrin. The resulting metal complex (Zn-DIGPor) potentiated the activity of the DNA-alkylating drug temozolomide in an MGMT-expressing cell line. To the best of our knowledge, this is the first example of DNA-targeted MGMT inhibition.<br /> (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1439-7633
Volume :
18
Issue :
10
Database :
MEDLINE
Journal :
Chembiochem : a European journal of chemical biology
Publication Type :
Academic Journal
Accession number :
28177192
Full Text :
https://doi.org/10.1002/cbic.201600652