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Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients
BACKGROUND: Nectin-4, also known as PVRL4 (poliovirus-receptor-like 4), is specifically expressed in the embryo and placenta. Recent studies have reported that the Nectin-4 is over-expressed in multiple human cancers, and such abnormal expression is associated with cancer progression and poor progno...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480822/ https://www.ncbi.nlm.nih.gov/pubmed/31043861 http://dx.doi.org/10.1186/s12935-019-0824-z |
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author | Deng, Haifeng Shi, Hongbing Chen, Lujun Zhou, You Jiang, Jingting |
author_facet | Deng, Haifeng Shi, Hongbing Chen, Lujun Zhou, You Jiang, Jingting |
author_sort | Deng, Haifeng |
collection | PubMed |
description | BACKGROUND: Nectin-4, also known as PVRL4 (poliovirus-receptor-like 4), is specifically expressed in the embryo and placenta. Recent studies have reported that the Nectin-4 is over-expressed in multiple human cancers, and such abnormal expression is associated with cancer progression and poor prognosis of the patients. In the present study, we aimed to characterize the expression pattern of Nectin-4 in human esophageal cancer (EC) tissues, and to investigate its clinical implications, prognostic value and regulatory effects on cellular functions of EC cells. METHODS: In the present study, we first examined Nectin-4 expression in human EC tissues by using immunohistochemistry (IHC) assay and analyzed the clinical associations. Then the cellular studies in vitro and the nude mice tumor model in vivo were used to examine the regulatory role of Nectin-4 in the progression of EC. RESULTS: Our results demonstrated that over-expression of Nectin-4 in human EC tissues was significantly associated with tumor size, depth of tumor invasion, and poor prognosis of the patients. The intervention of Nectin-4 expression in EC cell lines showed that the increased Nectin-4 expression could significantly promote the cell viability, migration, invasion and tumor formation. CONCLUSIONS: Our present data unveiled that Nectin-4 played an important role in tumor biology and could serve as a useful prognostic predictor of human EC. |
format | Online Article Text |
id | pubmed-6480822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64808222019-05-01 Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients Deng, Haifeng Shi, Hongbing Chen, Lujun Zhou, You Jiang, Jingting Cancer Cell Int Primary Research BACKGROUND: Nectin-4, also known as PVRL4 (poliovirus-receptor-like 4), is specifically expressed in the embryo and placenta. Recent studies have reported that the Nectin-4 is over-expressed in multiple human cancers, and such abnormal expression is associated with cancer progression and poor prognosis of the patients. In the present study, we aimed to characterize the expression pattern of Nectin-4 in human esophageal cancer (EC) tissues, and to investigate its clinical implications, prognostic value and regulatory effects on cellular functions of EC cells. METHODS: In the present study, we first examined Nectin-4 expression in human EC tissues by using immunohistochemistry (IHC) assay and analyzed the clinical associations. Then the cellular studies in vitro and the nude mice tumor model in vivo were used to examine the regulatory role of Nectin-4 in the progression of EC. RESULTS: Our results demonstrated that over-expression of Nectin-4 in human EC tissues was significantly associated with tumor size, depth of tumor invasion, and poor prognosis of the patients. The intervention of Nectin-4 expression in EC cell lines showed that the increased Nectin-4 expression could significantly promote the cell viability, migration, invasion and tumor formation. CONCLUSIONS: Our present data unveiled that Nectin-4 played an important role in tumor biology and could serve as a useful prognostic predictor of human EC. BioMed Central 2019-04-23 /pmc/articles/PMC6480822/ /pubmed/31043861 http://dx.doi.org/10.1186/s12935-019-0824-z 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 | Primary Research Deng, Haifeng Shi, Hongbing Chen, Lujun Zhou, You Jiang, Jingting Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
title | Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
title_full | Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
title_fullStr | Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
title_full_unstemmed | Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
title_short | Over-expression of Nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
title_sort | over-expression of nectin-4 promotes progression of esophageal cancer and correlates with poor prognosis of the patients |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480822/ https://www.ncbi.nlm.nih.gov/pubmed/31043861 http://dx.doi.org/10.1186/s12935-019-0824-z |
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