The apoptotic and genomic studies on A549 cell line induced by silver nitrate

Lung cancer is the leading cause of male cancer deaths worldwide. Metal-based anticancer drugs have evolved significantly during the past decades. Recently, silver ions have been investigated for their anticancer effects. We aimed to study the time-course cytotoxic effects of silver nitrate on A549...

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Main Authors: Ayse Kaplan, Gulsen Akalin Ciftci, Hatice Mehtap Kutlu
Format: Article
Language:English
Published: IOS Press 2017-04-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317695033
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spelling doaj-26eabfda731b4c959a2cfd689753dbfe2021-05-02T18:35:18ZengIOS PressTumor Biology1423-03802017-04-013910.1177/1010428317695033The apoptotic and genomic studies on A549 cell line induced by silver nitrateAyse Kaplan0Gulsen Akalin Ciftci1Hatice Mehtap Kutlu2Faculty of Science, Department of Biology, Anadolu University, Eskişehir, TurkeyFaculty of Pharmacy, Department of Biochemistry, Anadolu University, Eskişehir, TurkeyFaculty of Science, Department of Biology, Anadolu University, Eskişehir, TurkeyLung cancer is the leading cause of male cancer deaths worldwide. Metal-based anticancer drugs have evolved significantly during the past decades. Recently, silver ions have been investigated for their anticancer effects. We aimed to study the time-course cytotoxic effects of silver nitrate on A549 adenocarcinomic human alveolar basal epithelial cells to provide insights into the molecular-level understanding of growth suppression mechanism involved in apoptosis. The influences of silver nitrate were studied via MTT assay, flow cytometry, immunocytochemical, confocal and transmission electron microscopy, and microarray assays. Silver nitrate showed inhibitory effects against A549 cells in a dose- and time-dependent manner for 24, 48, and 72 h and induced apoptosis. The early and late apoptotic cells and depolarized mitochondrial membrane potential were determined by the half-maximal inhibitory concentration (IC 50 ) value of silver nitrate treated for 72 h. But cysteinyl aspartate proteinase-3 was not activated for 72 h. Furthermore, IC 50 value of silver nitrate also induced apoptosis according to immunocytochemical assays for 72 h. The downregulated CCNY , HNRNPL , ASF1B , PIAS4 , HNRNPH1 , EIF2C2 , TAF15 , FOXC1 , LEP , and PCB2 genes administered with silver nitrate IC 50 were identified as apoptosis-leading genes. Silver nitrate may be a suitable therapeutic agent against lung cancer.https://doi.org/10.1177/1010428317695033
collection DOAJ
language English
format Article
sources DOAJ
author Ayse Kaplan
Gulsen Akalin Ciftci
Hatice Mehtap Kutlu
spellingShingle Ayse Kaplan
Gulsen Akalin Ciftci
Hatice Mehtap Kutlu
The apoptotic and genomic studies on A549 cell line induced by silver nitrate
Tumor Biology
author_facet Ayse Kaplan
Gulsen Akalin Ciftci
Hatice Mehtap Kutlu
author_sort Ayse Kaplan
title The apoptotic and genomic studies on A549 cell line induced by silver nitrate
title_short The apoptotic and genomic studies on A549 cell line induced by silver nitrate
title_full The apoptotic and genomic studies on A549 cell line induced by silver nitrate
title_fullStr The apoptotic and genomic studies on A549 cell line induced by silver nitrate
title_full_unstemmed The apoptotic and genomic studies on A549 cell line induced by silver nitrate
title_sort apoptotic and genomic studies on a549 cell line induced by silver nitrate
publisher IOS Press
series Tumor Biology
issn 1423-0380
publishDate 2017-04-01
description Lung cancer is the leading cause of male cancer deaths worldwide. Metal-based anticancer drugs have evolved significantly during the past decades. Recently, silver ions have been investigated for their anticancer effects. We aimed to study the time-course cytotoxic effects of silver nitrate on A549 adenocarcinomic human alveolar basal epithelial cells to provide insights into the molecular-level understanding of growth suppression mechanism involved in apoptosis. The influences of silver nitrate were studied via MTT assay, flow cytometry, immunocytochemical, confocal and transmission electron microscopy, and microarray assays. Silver nitrate showed inhibitory effects against A549 cells in a dose- and time-dependent manner for 24, 48, and 72 h and induced apoptosis. The early and late apoptotic cells and depolarized mitochondrial membrane potential were determined by the half-maximal inhibitory concentration (IC 50 ) value of silver nitrate treated for 72 h. But cysteinyl aspartate proteinase-3 was not activated for 72 h. Furthermore, IC 50 value of silver nitrate also induced apoptosis according to immunocytochemical assays for 72 h. The downregulated CCNY , HNRNPL , ASF1B , PIAS4 , HNRNPH1 , EIF2C2 , TAF15 , FOXC1 , LEP , and PCB2 genes administered with silver nitrate IC 50 were identified as apoptosis-leading genes. Silver nitrate may be a suitable therapeutic agent against lung cancer.
url https://doi.org/10.1177/1010428317695033
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