Literature DB >> 24975085

Combination of therapy with 5-fluorouracil and cisplatin with electroporation in human ovarian carcinoma model in vitro.

Jolanta Saczko1, Iwona Kamińska2, Malgorzata Kotulska3, Julia Bar2, Anna Choromańska1, Nina Rembiałkowska1, Katarzyna Bieżuńska-Kusiak1, Joanna Rossowska4, Danuta Nowakowska5, Julita Kulbacka6.   

Abstract

High electric field, applied to plasma membrane, affects organization of the lipid molecules, generating transient hydrophilic electropores. The application of the cell membrane electroporation in combination with cytotoxic drugs could increase the drug transport into cells. This approach is known as electrochemotherapy (ECT). Our work shows new data concerning the influence of electrochemical reaction with cisplatin or with 5-fluorouracil (5-FU) on cancer ovarian cells resistant to standard therapy with cisplatin, in comparison to ECT effect on human primary fibroblasts. We investigated the effect of electroporation and electrochemotherapy with 5-FU and cisplatin on human ovarian clear-cell carcinoma cell line (OvBH-1) and epithelial ovarian carcinoma cell line (SKOV-3) - both resistant to cisplatin typically used in ovarian cancers. As control cells, human gingival fibroblasts (HGF's) from primary culture were used. Electropermeabilization efficiency was determined by FACS analysis with iodide propidium. Efficiency of electrochemotherapy was evaluated with viability assay. The cytotoxic effect was dependent on the electroporation parameters and on drug concentration. Electroporation alone only insignificantly decreased cells proliferation in OvBH-1 line; SKOV-3 line was more sensitive to the electrical field. Electrochemotherapy with cisplatin and 5-FU showed promising effects on both ovarian cell lines with recovery of normal cells revealed after 72 hours.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  5-fluorouracil; Cisplatin; Electrochemotherapy; Electropermeabilization; Human fibroblasts; Ovarian carcinoma

Mesh:

Substances:

Year:  2014        PMID: 24975085     DOI: 10.1016/j.biopha.2014.05.005

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  12 in total

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