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An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells
The present study aimed to investigate the anticancer effects of cisplatin (DDP) combined with salinomycin (SAL) on the gastric cancer cell line SGC-7901, as well as to explore the mechanisms underlying their actions. An MTT assay was used to evaluate the inhibitory effects of SAL, DDP and their com...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561897/ https://www.ncbi.nlm.nih.gov/pubmed/28627601 http://dx.doi.org/10.3892/mmr.2017.6731 |
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author | Zhang, Zuwen Zhao, Jumei Pang, Qiuxia Wang, Aihong Chen, Meini Wei, Xiaoli |
author_facet | Zhang, Zuwen Zhao, Jumei Pang, Qiuxia Wang, Aihong Chen, Meini Wei, Xiaoli |
author_sort | Zhang, Zuwen |
collection | PubMed |
description | The present study aimed to investigate the anticancer effects of cisplatin (DDP) combined with salinomycin (SAL) on the gastric cancer cell line SGC-7901, as well as to explore the mechanisms underlying their actions. An MTT assay was used to evaluate the inhibitory effects of SAL, DDP and their combination on gastric cancer cell proliferation. Morphological alterations of cancer cells following treatment were observed under an inverted phase-contrast microscope and a fluorescence microscope. Cell cycle progression and apoptosis were analyzed using flow cytometry. The expression of nuclear factor (NF)-κB p65 and Fas protein ligand (L) in cancer cells was assessed using immunocytochemistry. The present results demonstrated that the combination of SAL and DDP significantly inhibited the proliferation (P<0.05) and altered the morphological characteristics of SGC-7901 cells, thus suggesting that SAL may enhance the susceptibility of gastric cancer cells to DDP. In addition, treatment with a combination of SAL and DDP resulted in S phase-arrest and increased the apoptotic rate of SGC-7901 cells. Furthermore, marked FasL upregulation and NF-κB p65 downregulation were observed in cancer cells treated with the combination of SAL and DDP. The results of the present study demonstrated that the combination of SAL and DDP induced the apoptosis of human gastric cancer cells, and suggested that the underlying mechanism may involve the upregulation of FasL and downregulation of NF-κB p65. |
format | Online Article Text |
id | pubmed-5561897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-55618972017-10-23 An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells Zhang, Zuwen Zhao, Jumei Pang, Qiuxia Wang, Aihong Chen, Meini Wei, Xiaoli Mol Med Rep Articles The present study aimed to investigate the anticancer effects of cisplatin (DDP) combined with salinomycin (SAL) on the gastric cancer cell line SGC-7901, as well as to explore the mechanisms underlying their actions. An MTT assay was used to evaluate the inhibitory effects of SAL, DDP and their combination on gastric cancer cell proliferation. Morphological alterations of cancer cells following treatment were observed under an inverted phase-contrast microscope and a fluorescence microscope. Cell cycle progression and apoptosis were analyzed using flow cytometry. The expression of nuclear factor (NF)-κB p65 and Fas protein ligand (L) in cancer cells was assessed using immunocytochemistry. The present results demonstrated that the combination of SAL and DDP significantly inhibited the proliferation (P<0.05) and altered the morphological characteristics of SGC-7901 cells, thus suggesting that SAL may enhance the susceptibility of gastric cancer cells to DDP. In addition, treatment with a combination of SAL and DDP resulted in S phase-arrest and increased the apoptotic rate of SGC-7901 cells. Furthermore, marked FasL upregulation and NF-κB p65 downregulation were observed in cancer cells treated with the combination of SAL and DDP. The results of the present study demonstrated that the combination of SAL and DDP induced the apoptosis of human gastric cancer cells, and suggested that the underlying mechanism may involve the upregulation of FasL and downregulation of NF-κB p65. D.A. Spandidos 2017-08 2017-06-08 /pmc/articles/PMC5561897/ /pubmed/28627601 http://dx.doi.org/10.3892/mmr.2017.6731 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhang, Zuwen Zhao, Jumei Pang, Qiuxia Wang, Aihong Chen, Meini Wei, Xiaoli An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
title | An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
title_full | An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
title_fullStr | An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
title_full_unstemmed | An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
title_short | An in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
title_sort | in vitro study on the effects of the combination of salinomycin with cisplatin on human gastric cancer cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561897/ https://www.ncbi.nlm.nih.gov/pubmed/28627601 http://dx.doi.org/10.3892/mmr.2017.6731 |
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