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Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma
BACKGROUND: This study investigated the expression and biological function of JAB1 in esophageal squamous cell carcinoma (ESCC). METHODS: The expression of JAB1 in ESCC tissues and cells was measured using reverse transcriptase‐polymerase chain reaction (RT‐PCR), immunohistochemistry (IHC), and west...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113044/ https://www.ncbi.nlm.nih.gov/pubmed/32064781 http://dx.doi.org/10.1111/1759-7714.13350 |
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author | Shen, Qi Shang, Bin Jiang, Bin Wang, Yu Wang, Zhou Chen, Gang |
author_facet | Shen, Qi Shang, Bin Jiang, Bin Wang, Yu Wang, Zhou Chen, Gang |
author_sort | Shen, Qi |
collection | PubMed |
description | BACKGROUND: This study investigated the expression and biological function of JAB1 in esophageal squamous cell carcinoma (ESCC). METHODS: The expression of JAB1 in ESCC tissues and cells was measured using reverse transcriptase‐polymerase chain reaction (RT‐PCR), immunohistochemistry (IHC), and western blot analysis. Kaplan‐Meier survival analysis was performed to explore the effect of JAB1 expression on the prognosis of ESCC patients. Furthermore, experiments were conducted in vivo and in vitro to determine the effect of JAB1 expression on the malignant behavior of ESCC cells. RESULTS: Compared with adjacent tissues, JAB1 was highly overexpressed in cancer tissues (P = 0.01). Univariate and multivariate analyses of clinical data indicated that patients with JAB1 overexpression had a worse prognosis (P = 0.001 and P = 0.049, respectively). Cell function experiments and tumorigenesis experiments in nude mice showed that the upregulation of JAB1 might promote malignant behavior, and vice versa. CONCLUSIONS: Overexpression of JAB1 promoted the proliferation, migration, and invasion of ESCC cells, and was significantly associated with poor prognosis of ESCC patients. Therefore, JAB1 could be considered as a promising prognostic factor and a possible target for the specific therapy of ESCC. KEY POINTS: In this study, we found that JAB1 was highly overexpressed in cancer tissues, which could influence the malignant behavior of ESCC cells, and was significantly associated with poor prognosis of ESCC patients. |
format | Online Article Text |
id | pubmed-7113044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71130442020-04-02 Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma Shen, Qi Shang, Bin Jiang, Bin Wang, Yu Wang, Zhou Chen, Gang Thorac Cancer Original Articles BACKGROUND: This study investigated the expression and biological function of JAB1 in esophageal squamous cell carcinoma (ESCC). METHODS: The expression of JAB1 in ESCC tissues and cells was measured using reverse transcriptase‐polymerase chain reaction (RT‐PCR), immunohistochemistry (IHC), and western blot analysis. Kaplan‐Meier survival analysis was performed to explore the effect of JAB1 expression on the prognosis of ESCC patients. Furthermore, experiments were conducted in vivo and in vitro to determine the effect of JAB1 expression on the malignant behavior of ESCC cells. RESULTS: Compared with adjacent tissues, JAB1 was highly overexpressed in cancer tissues (P = 0.01). Univariate and multivariate analyses of clinical data indicated that patients with JAB1 overexpression had a worse prognosis (P = 0.001 and P = 0.049, respectively). Cell function experiments and tumorigenesis experiments in nude mice showed that the upregulation of JAB1 might promote malignant behavior, and vice versa. CONCLUSIONS: Overexpression of JAB1 promoted the proliferation, migration, and invasion of ESCC cells, and was significantly associated with poor prognosis of ESCC patients. Therefore, JAB1 could be considered as a promising prognostic factor and a possible target for the specific therapy of ESCC. KEY POINTS: In this study, we found that JAB1 was highly overexpressed in cancer tissues, which could influence the malignant behavior of ESCC cells, and was significantly associated with poor prognosis of ESCC patients. John Wiley & Sons Australia, Ltd 2020-02-16 2020-04 /pmc/articles/PMC7113044/ /pubmed/32064781 http://dx.doi.org/10.1111/1759-7714.13350 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Shen, Qi Shang, Bin Jiang, Bin Wang, Yu Wang, Zhou Chen, Gang Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
title | Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
title_full | Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
title_fullStr | Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
title_full_unstemmed | Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
title_short | Overexpression of JAB1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
title_sort | overexpression of jab1 promotes malignant behavior and predicts poor prognosis in esophageal squamous cell carcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113044/ https://www.ncbi.nlm.nih.gov/pubmed/32064781 http://dx.doi.org/10.1111/1759-7714.13350 |
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