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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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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