Novel Palladium Complex: Cytotoxicity against Cisplatin-resistant K562 Cells

(2019) Novel Palladium Complex: Cytotoxicity against Cisplatin-resistant K562 Cells. Iranian Journal of Pharmaceutical Research. pp. 1323-1331. ISSN 1735-0328

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Abstract

Today, development of resistance to anticancer drugs (including cisplatin) is noticed as a major problem. Recently several studies demonstrated that palladium complexes showed remarkable cytotoxic effects against K562 cell line and could be used efficiently for treatment of many human cancers including leukemia. Hereof, K562 cells were made resistant to cisplatin using increasing concentration of cisplatin up to 4.5 mM and then cytotoxic effect of synthesized palladium complex was evaluated on this sub-line using MTT assay. Annexin V/PI staining using flow cytometry and scanning electron microscopy (SEM) were performed to find out the mechanism of the observed cytotoxicity. Results indicated that tested compounds had a noticeable cytotoxic effect on K562 cells 80 times more than cisplatin. Palladium complex also showed significant cytotoxicity on resistant K562 sub-line. Flow cytometry and SEM results revealed that these compounds exert their cytotoxic effect via apoptosis and it could be concluded that the novel synthesized palladium complex might be a good candidate for replacing cisplatin in case of treatment of cisplatin resistant tumors.

Item Type: Article
Keywords: K562 cells Cisplatin resistance Palladacyclic complex MTT assay Apoptosis assay apoptosis design Pharmacology & Pharmacy
Subjects: QV Pharmacology
Divisions: Faculty of Pharmacy and Pharmaceutical Sciences > Department of Pharmaceutical Biotechnology
Faculty of Pharmacy and Pharmaceutical Sciences > گروه شیمی دارویی
Page Range: pp. 1323-1331
Journal or Publication Title: Iranian Journal of Pharmaceutical Research
Journal Index: ISI
Volume: 18
Number: 3
Identification Number: https://doi.org/10.22037/ijpr.2019.1100714
ISSN: 1735-0328
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/11130

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