Cargando…

Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT

BACKGROUND: Nicotinic acetylcholine receptors (nAChRs) have been reported to be overexpressed in malignancies in humans and is associated with tumorigenesis and cell migration. In previous studies of gastric cancer, alpha7 nicotinic acetylcholine receptor (α7-nAChR) overexpression leads to epithelia...

Descripción completa

Detalles Bibliográficos
Autores principales: Bu, Xuefeng, Zhang, Anwei, Chen, Zhengwei, Zhang, Xuanfeng, Zhang, Riting, Yin, Chaoyun, Zhang, Jie, Zhang, Yao, Yan, Yulan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805660/
https://www.ncbi.nlm.nih.gov/pubmed/31640627
http://dx.doi.org/10.1186/s12885-019-6225-9
_version_ 1783461443458301952
author Bu, Xuefeng
Zhang, Anwei
Chen, Zhengwei
Zhang, Xuanfeng
Zhang, Riting
Yin, Chaoyun
Zhang, Jie
Zhang, Yao
Yan, Yulan
author_facet Bu, Xuefeng
Zhang, Anwei
Chen, Zhengwei
Zhang, Xuanfeng
Zhang, Riting
Yin, Chaoyun
Zhang, Jie
Zhang, Yao
Yan, Yulan
author_sort Bu, Xuefeng
collection PubMed
description BACKGROUND: Nicotinic acetylcholine receptors (nAChRs) have been reported to be overexpressed in malignancies in humans and is associated with tumorigenesis and cell migration. In previous studies of gastric cancer, alpha7 nicotinic acetylcholine receptor (α7-nAChR) overexpression leads to epithelial-mesenchymal transition (EMT) and promotes the migration of gastric cancer cells. Recombinant avirulent LaSota strain of Newcastle disease virus (NDV) expressing the rabies virus glycoprotein (rL-RVG) may promote apoptosis of gastric cancer cells and reduces the migration of lung cancer metastasis. However, whether rL-RVG inhibits migration of gastric cancer cells and what the underlying functional mechanism is remains unknown. METHODS: The gastric cancer cell lines BGC and SGC were randomly divided into 3 groups: rL-RVG, NDV and Phosphate Buffered Solution (PBS) control groups. Furthermore,we adopted ACB and MLA,α7nAChR-siRNA for the overexpression and silencing of α7-nAChR.Corynoxenine was used for inhibiting the MEK-ERK pathway. Western blot, Immunofluoresce,cell proliferation assays,cell migration analyses through wound-healing assays and Transwell assays were used to explore the underlying mechanisms. A mouse xenograft model was used to investigate the effects of rL-RVG,NDV on tumor growth. RESULTS: In this study, our findings demonstrate that rL-RVG suppressed the migration of gastric cancer cells and reduced EMT via α7-nAChR in vitro. Furthermore rL-RVG decreased the phosphorylation levels of the MEK/ERK signaling pathway such as down-regulating the expression of P-MEK and P-ERK. Additionally, rL-RVG also reduced the expression level of mesenchymal markers N-cadherin and Vimentin and enhanced the expression of the epithelial marker E-cadherin. Lastly, rL-RVG inhibited nicotinic acetylcholine receptors (nAChRs) to suppress cell migration and epithelial to mesenchymal transition (EMT) in gastric cell. We also found that rL-RVG suppresses the growth of gastric cancer subcutaneous tumor cells in vivo. CONCLUSION: rL-RVG inhibits α7-nAChR-MEK/ERK-EMT to suppress migration of gastric cancer cells.
format Online
Article
Text
id pubmed-6805660
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-68056602019-10-24 Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT Bu, Xuefeng Zhang, Anwei Chen, Zhengwei Zhang, Xuanfeng Zhang, Riting Yin, Chaoyun Zhang, Jie Zhang, Yao Yan, Yulan BMC Cancer Research Article BACKGROUND: Nicotinic acetylcholine receptors (nAChRs) have been reported to be overexpressed in malignancies in humans and is associated with tumorigenesis and cell migration. In previous studies of gastric cancer, alpha7 nicotinic acetylcholine receptor (α7-nAChR) overexpression leads to epithelial-mesenchymal transition (EMT) and promotes the migration of gastric cancer cells. Recombinant avirulent LaSota strain of Newcastle disease virus (NDV) expressing the rabies virus glycoprotein (rL-RVG) may promote apoptosis of gastric cancer cells and reduces the migration of lung cancer metastasis. However, whether rL-RVG inhibits migration of gastric cancer cells and what the underlying functional mechanism is remains unknown. METHODS: The gastric cancer cell lines BGC and SGC were randomly divided into 3 groups: rL-RVG, NDV and Phosphate Buffered Solution (PBS) control groups. Furthermore,we adopted ACB and MLA,α7nAChR-siRNA for the overexpression and silencing of α7-nAChR.Corynoxenine was used for inhibiting the MEK-ERK pathway. Western blot, Immunofluoresce,cell proliferation assays,cell migration analyses through wound-healing assays and Transwell assays were used to explore the underlying mechanisms. A mouse xenograft model was used to investigate the effects of rL-RVG,NDV on tumor growth. RESULTS: In this study, our findings demonstrate that rL-RVG suppressed the migration of gastric cancer cells and reduced EMT via α7-nAChR in vitro. Furthermore rL-RVG decreased the phosphorylation levels of the MEK/ERK signaling pathway such as down-regulating the expression of P-MEK and P-ERK. Additionally, rL-RVG also reduced the expression level of mesenchymal markers N-cadherin and Vimentin and enhanced the expression of the epithelial marker E-cadherin. Lastly, rL-RVG inhibited nicotinic acetylcholine receptors (nAChRs) to suppress cell migration and epithelial to mesenchymal transition (EMT) in gastric cell. We also found that rL-RVG suppresses the growth of gastric cancer subcutaneous tumor cells in vivo. CONCLUSION: rL-RVG inhibits α7-nAChR-MEK/ERK-EMT to suppress migration of gastric cancer cells. BioMed Central 2019-10-22 /pmc/articles/PMC6805660/ /pubmed/31640627 http://dx.doi.org/10.1186/s12885-019-6225-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bu, Xuefeng
Zhang, Anwei
Chen, Zhengwei
Zhang, Xuanfeng
Zhang, Riting
Yin, Chaoyun
Zhang, Jie
Zhang, Yao
Yan, Yulan
Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT
title Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT
title_full Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT
title_fullStr Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT
title_full_unstemmed Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT
title_short Migration of gastric cancer is suppressed by recombinant Newcastle disease virus (rL-RVG) via regulating α7-nicotinic acetylcholine receptors/ERK- EMT
title_sort migration of gastric cancer is suppressed by recombinant newcastle disease virus (rl-rvg) via regulating α7-nicotinic acetylcholine receptors/erk- emt
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805660/
https://www.ncbi.nlm.nih.gov/pubmed/31640627
http://dx.doi.org/10.1186/s12885-019-6225-9
work_keys_str_mv AT buxuefeng migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT zhanganwei migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT chenzhengwei migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT zhangxuanfeng migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT zhangriting migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT yinchaoyun migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT zhangjie migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT zhangyao migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt
AT yanyulan migrationofgastriccancerissuppressedbyrecombinantnewcastlediseasevirusrlrvgviaregulatinga7nicotinicacetylcholinereceptorserkemt