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, II | 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 | 2015-11-24T19:36:06Z | |
dc.date.available | 2015-11-24T19:36:06Z | |
dc.identifier.issn | 1879-0720 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/23806 | |
dc.rights | Default Licence | - |
dc.subject | Animals | en |
dc.subject | Antineoplastic Agents/chemistry/*pharmacology | en |
dc.subject | Apoptosis/drug effects | en |
dc.subject | Cell Line, Tumor | en |
dc.subject | Drug Screening Assays, Antitumor | en |
dc.subject | Female | en |
dc.subject | Flow Cytometry | en |
dc.subject | Humans | en |
dc.subject | Neoplasms, Experimental/*pathology | en |
dc.subject | Nicotinic Acids/chemistry/*pharmacology | en |
dc.subject | Organotin Compounds/chemistry/*pharmacology | en |
dc.subject | Platelet Aggregation/drug effects | en |
dc.subject | Rats | en |
dc.subject | Rats, Wistar | en |
dc.subject | Sulfhydryl Compounds/chemistry/*pharmacology | 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 80mg/kgBody Weight (BW) or four repeated doses of 8mg/kgBW once per week. Furthermore, antitumor activity studies on sarcoma bearing Wistar rats revealed that SnMNA complex at four repeated doses of 5.4mg/kgBW 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. | en |
heal.access | campus | - |
heal.fullTextAvailability | TRUE | - |
heal.identifier.primary | 10.1016/j.ejps.2010.11.015 | - |
heal.identifier.secondary | http://www.ncbi.nlm.nih.gov/pubmed/21130873 | - |
heal.identifier.secondary | http://www.sciencedirect.com/science/article/pii/S092809871000391X | - |
heal.journalName | Eur J Pharm Sci | en |
heal.journalType | peer-reviewed | - |
heal.language | en | - |
heal.publicationDate | 2011 | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής | el |
heal.type | journalArticle | - |
heal.type.el | Άρθρο Περιοδικού | el |
heal.type.en | Journal article | en |
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