Anticancer and cytotoxic effects of a triorganotin compound with 2-mercapto-nicotinic acid in malignant cell lines and tumor bearing Wistar rats
dc.contributor.author | Verginadis, I. I. | en |
dc.contributor.author | Karkabounas, S. | en |
dc.contributor.author | Simos, Y. | en |
dc.contributor.author | Kontargiris, E. | en |
dc.contributor.author | Hadjikakou, S. K. | en |
dc.contributor.author | Batistatou, A. | en |
dc.contributor.author | Evangelou, A. | en |
dc.contributor.author | Charalabopoulos, K. | en |
dc.date.accessioned | 2015-11-24T16:50:53Z | |
dc.date.available | 2015-11-24T16:50:53Z | |
dc.identifier.issn | 0928-0987 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9655 | |
dc.rights | Default Licence | - |
dc.subject | triorganotin | en |
dc.subject | tin complexes | en |
dc.subject | cytotoxicity | en |
dc.subject | apoptosis | en |
dc.subject | anticancer drugs | en |
dc.subject | in-vitro | en |
dc.subject | organotin compound | en |
dc.subject | antitumor-activity | en |
dc.subject | cervical-cancer | en |
dc.subject | structural-characterization | en |
dc.subject | diorganotin(iv) compounds | en |
dc.subject | alkyl series | en |
dc.subject | dimethyl tin | en |
dc.subject | complexes | en |
dc.subject | vivo | en |
dc.title | Anticancer and cytotoxic effects of a triorganotin compound with 2-mercapto-nicotinic acid in malignant cell lines and tumor bearing Wistar rats | en |
heal.abstract | Nowadays, investigation for possible therapeutic applications of various metal-based drugs attracts the scientific interest worldwide. The triorganotin compound bis[triphenyltin(IV)](3-carboxy-pyridine-2-thionato) (SnMNA), was tested for its anti-proliferative and antitumor activities. Cytotoxic activity was assessed by Trypan blue and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay (MTT). SnMNA exhibited potent cytotoxic effects against leiomyosarcoma cells (LMS) and human breast adenocarcinoma cells (MCF-7), which is 200 times stronger than that of cisplatin. Moreover, SnMNA induced significant apoptosis in LMS and MCF-7 cells characterized by flow cytometry analysis and DNA fragmentation. Acute and chronic toxicity studies on Wistar rats caused kidney and lung toxicity at a single dose of 80 mg/kg Body Weight (BW) or four repeated doses of 8 mg/kg BW once per week. Furthermore, antitumor activity studies on sarcoma bearing Wistar rats revealed that SnMNA complex at four repeated doses of 5.4 mg/kg BW every three days prolonged mean survival time of the animal at 200% and decreased mean tumor growth rate (MTGR) compared to the control group (p < 0.05). It is noteworthy to mention that the 30% (3 out of 10) of the bearing animals were totally cured. These findings indicate that SnMNA might be a promising new antitumor agent. (C) 2010 Elsevier B.V. All rights reserved. | en |
heal.access | campus | - |
heal.fullTextAvailability | TRUE | - |
heal.identifier.primary | DOI 10.1016/j.ejps.2010.11.015 | - |
heal.identifier.secondary | <Go to ISI>://000287616300010 | - |
heal.identifier.secondary | http://ac.els-cdn.com/S092809871000391X/1-s2.0-S092809871000391X-main.pdf?_tid=984ac33c127a1dbce2008d671cd82c5e&acdnat=1333030284_9ab8b2b400cf2bdd817630ea1acce56e | - |
heal.journalName | European Journal of Pharmaceutical Sciences | en |
heal.journalType | peer reviewed | - |
heal.language | en | - |
heal.publicationDate | 2011 | - |
heal.publisher | Elsevier | en |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.type | journalArticle | - |
heal.type.el | Άρθρο Περιοδικού | el |
heal.type.en | Journal article | en |
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