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Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity

Cisplatin is one of the most useful chemotherapeutics which performs its cytotoxic effect via accumulation of platinum resulting in oxidative stress, and destruction of cell DNA. This could probably cause secondary cancers in healthy tissues. Lipocalin2 (Lcn2) is a protein which its expression is in...

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Autores principales: Sadeghi, Fatemeh, Etebari, Mahmoud, Habibi Roudkenar, Mehryar, Jahanian-Najafabadi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937086/
https://www.ncbi.nlm.nih.gov/pubmed/29755547
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author Sadeghi, Fatemeh
Etebari, Mahmoud
Habibi Roudkenar, Mehryar
Jahanian-Najafabadi, Ali
author_facet Sadeghi, Fatemeh
Etebari, Mahmoud
Habibi Roudkenar, Mehryar
Jahanian-Najafabadi, Ali
author_sort Sadeghi, Fatemeh
collection PubMed
description Cisplatin is one of the most useful chemotherapeutics which performs its cytotoxic effect via accumulation of platinum resulting in oxidative stress, and destruction of cell DNA. This could probably cause secondary cancers in healthy tissues. Lipocalin2 (Lcn2) is a protein which its expression is increased in oxidative stresses. Therefore, the present study was performed to evaluate the protective effects of Lcn2 up-regulation on cisplatin genotoxicity. In order to up-regulate Lcn2 expression, HEK293 cells were transfected with pcDNA3.1-Lcn2 vector. Afterwards, stable cells consistently expressing Lcn2 were selected via screening with G418 antibiotic. Next, overexpression of Lcn2 was evaluated by RT-PCR and ELISA, comparing to the control non-transfected cells. Then, in order to evaluate the cytoprotective effects of Lcn2 overexpression, transfected and non-transfected cells were subjected to cisplatin treatment followed by MTT and alkaline Comet assays. RT-PCR and ELISA assays confirmed up-regulation of Lcn2 by the stable cells. MTT assay of the Lcn2 over-expressing cells showed higher IC50 values comparing to the non-transfected cells. Furthermore, the Comet assay confirmed Lcn2 protective effects on the cisplatin (1 µg/mL) induced genotoxicity. In the present study, for the first time, we showed the protective effect of Lcn2 on cisplatin induced genotoxicity. Therefore, one of the probable mechanisms of Lcn2 cytoprotctive effects under oxidative stress conditions could be due to the prevention of genotoxicity. However, further evaluations in this regard must be considered.
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spelling pubmed-59370862018-05-11 Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity Sadeghi, Fatemeh Etebari, Mahmoud Habibi Roudkenar, Mehryar Jahanian-Najafabadi, Ali Iran J Pharm Res Original Article Cisplatin is one of the most useful chemotherapeutics which performs its cytotoxic effect via accumulation of platinum resulting in oxidative stress, and destruction of cell DNA. This could probably cause secondary cancers in healthy tissues. Lipocalin2 (Lcn2) is a protein which its expression is increased in oxidative stresses. Therefore, the present study was performed to evaluate the protective effects of Lcn2 up-regulation on cisplatin genotoxicity. In order to up-regulate Lcn2 expression, HEK293 cells were transfected with pcDNA3.1-Lcn2 vector. Afterwards, stable cells consistently expressing Lcn2 were selected via screening with G418 antibiotic. Next, overexpression of Lcn2 was evaluated by RT-PCR and ELISA, comparing to the control non-transfected cells. Then, in order to evaluate the cytoprotective effects of Lcn2 overexpression, transfected and non-transfected cells were subjected to cisplatin treatment followed by MTT and alkaline Comet assays. RT-PCR and ELISA assays confirmed up-regulation of Lcn2 by the stable cells. MTT assay of the Lcn2 over-expressing cells showed higher IC50 values comparing to the non-transfected cells. Furthermore, the Comet assay confirmed Lcn2 protective effects on the cisplatin (1 µg/mL) induced genotoxicity. In the present study, for the first time, we showed the protective effect of Lcn2 on cisplatin induced genotoxicity. Therefore, one of the probable mechanisms of Lcn2 cytoprotctive effects under oxidative stress conditions could be due to the prevention of genotoxicity. However, further evaluations in this regard must be considered. Shaheed Beheshti University of Medical Sciences 2018 /pmc/articles/PMC5937086/ /pubmed/29755547 Text en © 2018 by School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sadeghi, Fatemeh
Etebari, Mahmoud
Habibi Roudkenar, Mehryar
Jahanian-Najafabadi, Ali
Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity
title Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity
title_full Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity
title_fullStr Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity
title_full_unstemmed Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity
title_short Lipocalin2 Protects Human Embryonic Kidney Cells against Cisplatin–Induced Genotoxicity
title_sort lipocalin2 protects human embryonic kidney cells against cisplatin–induced genotoxicity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937086/
https://www.ncbi.nlm.nih.gov/pubmed/29755547
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