Activation of trans geometry in bifunctional mononuclear platinum complexes by a piperidine ligand. Mechanistic studies on antitumor action
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12970368
DOI
10.1074/jbc.m304720200
PII: S0021-9258(20)75775-3
Knihovny.cz E-zdroje
- MeSH
- adukty DNA chemie MeSH
- antitumorózní látky farmakologie MeSH
- časové faktory MeSH
- chemické modely MeSH
- CHO buňky MeSH
- cisplatina farmakokinetika MeSH
- DNA-polymerasa I chemie MeSH
- DNA chemie MeSH
- HeLa buňky MeSH
- HIV reverzní transkriptasa chemie MeSH
- hydroxylový radikál MeSH
- křečci praví MeSH
- lidé MeSH
- ligandy MeSH
- molekulární sekvence - údaje MeSH
- oligonukleotidy chemie MeSH
- piperidiny chemie MeSH
- platina chemie MeSH
- reagencia zkříženě vázaná farmakologie MeSH
- sekvence nukleotidů MeSH
- teoretické modely MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- křečci praví MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adukty DNA MeSH
- antitumorózní látky MeSH
- cisplatina MeSH
- DNA-polymerasa I MeSH
- DNA MeSH
- HIV reverzní transkriptasa MeSH
- hydroxylový radikál MeSH
- ligandy MeSH
- oligonukleotidy MeSH
- piperidine MeSH Prohlížeč
- piperidiny MeSH
- platina MeSH
- reagencia zkříženě vázaná MeSH
- transplatin MeSH Prohlížeč
A paradigm for the structure-pharmacological activity relationship of bifunctional platinum antitumor drugs is that the trans isomer of antitumor cisplatin (transplatin) is clinically ineffective. To this end, however, several new complexes of the trans structure have been identified that exhibit cytotoxicity in tumor cells that is even better than that of the analogous cis isomers. We reported recently (Kasparkova, J., Marini, V., Najajreh, Y., Gibson, D., and Brabec, V. (2003) Biochemistry 42, 6321-6332) that the replacement of one ammine ligand by the heterocyclic ligand, such as piperidine, piperazine, or 4-picoline in the molecule of transplatin resulted in a radical enhancement of its cytotoxicity. We examined oligodeoxyribonucleotide duplexes bearing a site-specific cross-link of the transplatin analogue containing the piperidine ligand by biochemical methods. The results indicate that in contrast to transplatin, trans-(PtCl2(NH3)(piperidine)) forms stable 1,3-intrastrand cross-links in double-helical DNA that distort DNA and are not readily removed from DNA by nucleotide excision repair system. Hence, the intrastrand cross-links of trans-(PtCl2(NH3)(piperidine)) could persist for a sufficiently long time, potentiating its toxicity toward tumor cells. trans-(PtCl2(NH3)(piperidine)) also forms in DNA minor interstrand cross-links that are similar to those of transplatin so that these adducts appear less likely candidates for genotoxic lesion responsible for antitumor effects of trans-(PtCl2(NH3)(piperidine)). Hence, the role of structurally unique intrastrand cross-links in the anti-tumor effects of transplatin analogues in which one ammine group is replaced by a heterocyclic ligand may predominate.
Citace poskytuje Crossref.org
Mechanism of the formation of DNA-protein cross-links by antitumor cisplatin