In vivo effect of cis- and trans-diamminedichloroplatinum(II) on DNA and chromatin degradation in Ehrlich ascites tumour cells
- PMID: 1291196
In vivo effect of cis- and trans-diamminedichloroplatinum(II) on DNA and chromatin degradation in Ehrlich ascites tumour cells
Abstract
Ehrlich ascites tumour (EAT) cell nuclei were isolated from mice treated with cis- and trans-diamminedichloroplatinum(II) (DDP). The electrophoretic analysis of DNA extracted from corresponding nuclei revealed the high level of EAT DNA stability suggesting very low DNA endonuclease activity. The DNA degradation to high molecular weight fragments was achieved by mild treatment of nuclei with exonuclease DNase I. Cis- and trans-DDP reduced the rate of EAT DNA breakdown to high molecular weight fragments. Direct gel electrophoresis of the same nuclei confirm and extend our recent finding of rat liver chromatin breakdown to large chromatin blocks of uniform size.
Similar articles
-
Endogenous degradation of DNA and chromatin in rat liver nuclei after in vivo treatment with cis- and trans-diamminedichloroplatinum (II).Cytobios. 1990;62(250-251):167-74. Cytobios. 1990. PMID: 2171880
-
Effect of cis-diamminedichloroplatinum(II) and other platinum compounds on the RNA polymerase reaction.Cytobios. 1994;77(309):81-6. Cytobios. 1994. PMID: 8020247
-
Properties of single-stranded DNA-binding proteins (SSB-proteins) from chromatin and nonchromatin fractions of Ehrlich ascites tumour: phosphorylation enhances the affinity of SSB-proteins for single-stranded DNA.Indian J Biochem Biophys. 1992 Feb;29(1):13-9. Indian J Biochem Biophys. 1992. PMID: 1592412
-
[Molecular and cellular aspects of cis-diamminedichloroplatinum (II) interactions with DNA].Postepy Hig Med Dosw. 1993;47(2):103-23. Postepy Hig Med Dosw. 1993. PMID: 8415320 Review. Polish.
-
Trans-diammineplatinum(II): what makes it different from cis-DDP? Coordination chemistry of a neglected relative of cisplatin and its interaction with nucleic acids.Met Ions Biol Syst. 1996;33:105-41. Met Ions Biol Syst. 1996. PMID: 8742842 Review.