The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines

There have been many studies on improving the efficacy of cisplatin and on identifying safe compounds that can overcome multi-drug resistance (MDR) acquired by cancer cells. Our previous research showed that polyethylene glycol-modified titanium dioxide nanoparticles (TiO<sub>2</sub> PEG...

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Main Authors: Basma Salama, El-Said El-Sherbini, Gehad El-Sayed, Mohamed El-Adl, Koki Kanehira, Akiyoshi Taniguchi
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/2/605
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author Basma Salama
El-Said El-Sherbini
Gehad El-Sayed
Mohamed El-Adl
Koki Kanehira
Akiyoshi Taniguchi
author_facet Basma Salama
El-Said El-Sherbini
Gehad El-Sayed
Mohamed El-Adl
Koki Kanehira
Akiyoshi Taniguchi
author_sort Basma Salama
collection DOAJ
description There have been many studies on improving the efficacy of cisplatin and on identifying safe compounds that can overcome multi-drug resistance (MDR) acquired by cancer cells. Our previous research showed that polyethylene glycol-modified titanium dioxide nanoparticles (TiO<sub>2</sub> PEG NPs) affect cell membrane receptors, resulting in their aggregation, altered localization and downregulation. TiO<sub>2</sub> PEG NPs may affect P-glycoprotein (P-gp), a membrane efflux channel involved in MDR. In this study, we investigated the effect of TiO<sub>2</sub> PEG NPs on cisplatin cytotoxicity. We used HepG2 cells, which highly express P-gp and A431 cells, which show low expression of P-gp. The results showed that 10 &#181;g/mL 100 nm TiO<sub>2</sub> PEG NPs increased intracellular cisplatin levels and cytotoxicity in HepG2 cells but not in A431 cells. TiO<sub>2</sub> PEG NPs treatment decreased the expression level of P-gp in HepG2 cells. Our findings indicate that TiO<sub>2</sub> PEG NPs enhance cisplatin cytotoxicity by down regulating P-gp and that TiO<sub>2</sub> PEG NPs are promising candidates for inhibiting P-gp and reversing drug resistance acquired by cancer cells.
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spelling doaj.art-cf7f0d7df4b64f7c883c18e74bec496b2022-12-22T02:52:19ZengMDPI AGInternational Journal of Molecular Sciences1422-00672020-01-0121260510.3390/ijms21020605ijms21020605The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell LinesBasma Salama0El-Said El-Sherbini1Gehad El-Sayed2Mohamed El-Adl3Koki Kanehira4Akiyoshi Taniguchi5Cellular Functional Nano Biomaterials Group, Research Center for Biomaterials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, JapanDepartment of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Mansoura University, 60 El Gomhouria St., Mansoura, Dakahlia Governorate 35516, EgyptDepartment of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Mansoura University, 60 El Gomhouria St., Mansoura, Dakahlia Governorate 35516, EgyptDepartment of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Mansoura University, 60 El Gomhouria St., Mansoura, Dakahlia Governorate 35516, EgyptCellular Functional Nano Biomaterials Group, Research Center for Biomaterials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, JapanCellular Functional Nano Biomaterials Group, Research Center for Biomaterials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, JapanThere have been many studies on improving the efficacy of cisplatin and on identifying safe compounds that can overcome multi-drug resistance (MDR) acquired by cancer cells. Our previous research showed that polyethylene glycol-modified titanium dioxide nanoparticles (TiO<sub>2</sub> PEG NPs) affect cell membrane receptors, resulting in their aggregation, altered localization and downregulation. TiO<sub>2</sub> PEG NPs may affect P-glycoprotein (P-gp), a membrane efflux channel involved in MDR. In this study, we investigated the effect of TiO<sub>2</sub> PEG NPs on cisplatin cytotoxicity. We used HepG2 cells, which highly express P-gp and A431 cells, which show low expression of P-gp. The results showed that 10 &#181;g/mL 100 nm TiO<sub>2</sub> PEG NPs increased intracellular cisplatin levels and cytotoxicity in HepG2 cells but not in A431 cells. TiO<sub>2</sub> PEG NPs treatment decreased the expression level of P-gp in HepG2 cells. Our findings indicate that TiO<sub>2</sub> PEG NPs enhance cisplatin cytotoxicity by down regulating P-gp and that TiO<sub>2</sub> PEG NPs are promising candidates for inhibiting P-gp and reversing drug resistance acquired by cancer cells.https://www.mdpi.com/1422-0067/21/2/605titanium dioxide nanoparticlescisplatincytotoxicitydrug resistancep-glycoprotein
spellingShingle Basma Salama
El-Said El-Sherbini
Gehad El-Sayed
Mohamed El-Adl
Koki Kanehira
Akiyoshi Taniguchi
The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines
International Journal of Molecular Sciences
titanium dioxide nanoparticles
cisplatin
cytotoxicity
drug resistance
p-glycoprotein
title The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines
title_full The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines
title_fullStr The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines
title_full_unstemmed The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines
title_short The Effects of TiO<sub>2</sub> Nanoparticles on Cisplatin Cytotoxicity in Cancer Cell Lines
title_sort effects of tio sub 2 sub nanoparticles on cisplatin cytotoxicity in cancer cell lines
topic titanium dioxide nanoparticles
cisplatin
cytotoxicity
drug resistance
p-glycoprotein
url https://www.mdpi.com/1422-0067/21/2/605
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