Comparative anti-tumor efficacy of two orally administered platinum(IV) drugs in nude mice bearing human tumor xenografts
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
16428939
DOI
10.1097/00001813-200602000-00012
PII: 00001813-200602000-00012
Knihovny.cz E-zdroje
- MeSH
- amantadin analogy a deriváty terapeutické užití MeSH
- chemorezistence MeSH
- cisplatina škodlivé účinky MeSH
- ligandy MeSH
- myši nahé MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- nádory prostaty farmakoterapie patologie prevence a kontrola MeSH
- nádory tračníku farmakoterapie patologie prevence a kontrola MeSH
- nádory vaječníků farmakoterapie patologie prevence a kontrola MeSH
- organoplatinové sloučeniny terapeutické užití MeSH
- protinádorové látky terapeutické užití MeSH
- transplantace heterologní MeSH
- viabilita buněk účinky léků MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- amantadin MeSH
- bis(acetato)(1-adamantylamine)amminedichloroplatinum(IV) MeSH Prohlížeč
- cisplatina MeSH
- ligandy MeSH
- organoplatinové sloučeniny MeSH
- protinádorové látky MeSH
- satraplatin MeSH Prohlížeč
The oral anti-tumor activity of a novel platinum(IV) complex, coded as LA-12, with a bulky adamantylamine ligand was evaluated and compared with another platinum(IV) complex satraplatin. The human carcinoma xenografts of colon HCT116, prostate PC3, and ovarian A2780 and A2780/cisR (resistant to cisplatin) were used to evaluate the in-vivo anti-tumor activity. The daily x 5 repeated dose regimen in equimolar doses of LA-12 and satraplatin, administered in 2 cycles, was selected for this evaluation. All doses of LA-12 and satraplatin were significantly effective in comparison with the control. The activities of LA-12 in all doses and all used tumor xenografts were higher than equimolar doses of satraplatin. The highest effect was reached with LA-12 at a dose of 60 mg/kg. The shapes of growth curves of ovarian carcinoma A2780 and its subline resistant to cisplatin after therapy with LA-12 were very similar. This shows that LA-12 is able to overcome resistance to cisplatin.
Citace poskytuje Crossref.org
The new platinum-based anticancer agent LA-12 induces retinol binding protein 4 in vivo