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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...

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Autores principales: Zhang, Zuwen, Zhao, Jumei, Pang, Qiuxia, Wang, Aihong, Chen, Meini, Wei, Xiaoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
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.
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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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