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Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells

The aim of the present study was to explore the effect of esophageal cancer-related gene 2 (ECRG2) protein in combination with cisplatin (DDP) on the proliferation and apoptosis of esophageal cancer cells. A 3-(4, 5-dimethylthiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT) assay was used to examin...

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Autores principales: SONG, HAI-YAN, DENG, XIAO-HUI, HOU, XIN-FANG, YUAN, GUO-YAN, ZHU, ZHEN-DONG, REN, MING-XIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186322/
https://www.ncbi.nlm.nih.gov/pubmed/25289046
http://dx.doi.org/10.3892/etm.2014.1972
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author SONG, HAI-YAN
DENG, XIAO-HUI
HOU, XIN-FANG
YUAN, GUO-YAN
ZHU, ZHEN-DONG
REN, MING-XIN
author_facet SONG, HAI-YAN
DENG, XIAO-HUI
HOU, XIN-FANG
YUAN, GUO-YAN
ZHU, ZHEN-DONG
REN, MING-XIN
author_sort SONG, HAI-YAN
collection PubMed
description The aim of the present study was to explore the effect of esophageal cancer-related gene 2 (ECRG2) protein in combination with cisplatin (DDP) on the proliferation and apoptosis of esophageal cancer cells. A 3-(4, 5-dimethylthiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT) assay was used to examine the effects of ECRG2 alone and ECRG2 in combination with DDP on the proliferation of EC9706 esophageal cancer cells. Hoechst 33258 staining was performed to analyze the effects of ECRG2 alone and ECRG2 in combination with DDP on apoptosis in the EC9706 cells. The expression levels of Bcl-2-associated X protein (Bax) mRNA and protein were determined by reverse transcription polymerase chain reaction (RT-PCR) and western blot analysis, respectively. The results from the MTT assay revealed that ECRG2 inhibited the proliferation of EC9706 cells and that ECRG2 in combination with DDP had a greater inhibitory effect on cell proliferation. The antiproliferative effects were time- and concentration-dependent, within a certain range of concentrations. The Hoechst 33258 staining results demonstrated that the number of apoptotic cells following treatment with ECRG2 in combination with DDP for 24 h was higher than that following treatment with ECRG2 alone for the same duration. Western blot analysis and RT-PCR results revealed that the expression levels of Bax mRNA and protein were upregulated in cells treated with ECRG2 in combination with DDP compared with those in cells treated with ECRG2 alone. Thus, ECRG2 in combination with DDP had an enhanced inhibitory effect on EC9706 cell proliferation compared with that of ECRG2 alone, and an increased inductive effect on EC9706 cell apoptosis, possibly due to the upregulation of the expression of Bax.
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spelling pubmed-41863222014-10-06 Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells SONG, HAI-YAN DENG, XIAO-HUI HOU, XIN-FANG YUAN, GUO-YAN ZHU, ZHEN-DONG REN, MING-XIN Exp Ther Med Articles The aim of the present study was to explore the effect of esophageal cancer-related gene 2 (ECRG2) protein in combination with cisplatin (DDP) on the proliferation and apoptosis of esophageal cancer cells. A 3-(4, 5-dimethylthiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT) assay was used to examine the effects of ECRG2 alone and ECRG2 in combination with DDP on the proliferation of EC9706 esophageal cancer cells. Hoechst 33258 staining was performed to analyze the effects of ECRG2 alone and ECRG2 in combination with DDP on apoptosis in the EC9706 cells. The expression levels of Bcl-2-associated X protein (Bax) mRNA and protein were determined by reverse transcription polymerase chain reaction (RT-PCR) and western blot analysis, respectively. The results from the MTT assay revealed that ECRG2 inhibited the proliferation of EC9706 cells and that ECRG2 in combination with DDP had a greater inhibitory effect on cell proliferation. The antiproliferative effects were time- and concentration-dependent, within a certain range of concentrations. The Hoechst 33258 staining results demonstrated that the number of apoptotic cells following treatment with ECRG2 in combination with DDP for 24 h was higher than that following treatment with ECRG2 alone for the same duration. Western blot analysis and RT-PCR results revealed that the expression levels of Bax mRNA and protein were upregulated in cells treated with ECRG2 in combination with DDP compared with those in cells treated with ECRG2 alone. Thus, ECRG2 in combination with DDP had an enhanced inhibitory effect on EC9706 cell proliferation compared with that of ECRG2 alone, and an increased inductive effect on EC9706 cell apoptosis, possibly due to the upregulation of the expression of Bax. D.A. Spandidos 2014-11 2014-09-17 /pmc/articles/PMC4186322/ /pubmed/25289046 http://dx.doi.org/10.3892/etm.2014.1972 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
SONG, HAI-YAN
DENG, XIAO-HUI
HOU, XIN-FANG
YUAN, GUO-YAN
ZHU, ZHEN-DONG
REN, MING-XIN
Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells
title Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells
title_full Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells
title_fullStr Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells
title_full_unstemmed Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells
title_short Effect of ECRG2 in combination with cisplatin on the proliferation and apoptosis of EC9706 cells
title_sort effect of ecrg2 in combination with cisplatin on the proliferation and apoptosis of ec9706 cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186322/
https://www.ncbi.nlm.nih.gov/pubmed/25289046
http://dx.doi.org/10.3892/etm.2014.1972
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