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Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer
AIM: The clinical implications of transforming growth factor-beta–induced gene-h3 (beta-IGH3) protein expression in lung cancer remain unclear. This study investigated beta-IGH3 protein expression levels and biological function, as well as lung cancer prognosis. METHODS: Beta-IGH3 protein expression...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986675/ https://www.ncbi.nlm.nih.gov/pubmed/27563252 http://dx.doi.org/10.2147/OTT.S100102 |
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author | He, Changjun Sun, Dawei Bai, Xue Li, Yingbin Xu, Hai Xu, Shidong |
author_facet | He, Changjun Sun, Dawei Bai, Xue Li, Yingbin Xu, Hai Xu, Shidong |
author_sort | He, Changjun |
collection | PubMed |
description | AIM: The clinical implications of transforming growth factor-beta–induced gene-h3 (beta-IGH3) protein expression in lung cancer remain unclear. This study investigated beta-IGH3 protein expression levels and biological function, as well as lung cancer prognosis. METHODS: Beta-IGH3 protein expression levels were measured in 236 lung cancers and were matched with adjacent noncancerous tissues by immunohistochemical staining. Subsequently, the relationship between beta-IGH3 protein expression, clinical–pathological parameters, and lung cancer prognosis was evaluated. RESULTS: Beta-IGH3 protein expression was significantly higher in lung cancer tissues compared with adjacent noncancerous tissues (61.86% vs 22.88%; P=0.01). Of the 236 enrolled cases, 146 (61.86%) showed high beta-IGH3 levels. Tumor size, clinical stage, and lymph node metastasis were significantly related to beta-IGH3 protein expression in univariate analysis (P=0.001, 0.044, and 0.029, respectively), whereas age, sex, and histological type were not (P=0.038, 0.756, and 0.889, respectively). Finally, a Cox regression model also identified beta-IGH3 as an independent prognostic factor (P=0.01). CONCLUSION: Beta-IGH3 is highly expressed in lung cancers and may be a potential target for lung cancer treatments. |
format | Online Article Text |
id | pubmed-4986675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49866752016-08-25 Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer He, Changjun Sun, Dawei Bai, Xue Li, Yingbin Xu, Hai Xu, Shidong Onco Targets Ther Original Research AIM: The clinical implications of transforming growth factor-beta–induced gene-h3 (beta-IGH3) protein expression in lung cancer remain unclear. This study investigated beta-IGH3 protein expression levels and biological function, as well as lung cancer prognosis. METHODS: Beta-IGH3 protein expression levels were measured in 236 lung cancers and were matched with adjacent noncancerous tissues by immunohistochemical staining. Subsequently, the relationship between beta-IGH3 protein expression, clinical–pathological parameters, and lung cancer prognosis was evaluated. RESULTS: Beta-IGH3 protein expression was significantly higher in lung cancer tissues compared with adjacent noncancerous tissues (61.86% vs 22.88%; P=0.01). Of the 236 enrolled cases, 146 (61.86%) showed high beta-IGH3 levels. Tumor size, clinical stage, and lymph node metastasis were significantly related to beta-IGH3 protein expression in univariate analysis (P=0.001, 0.044, and 0.029, respectively), whereas age, sex, and histological type were not (P=0.038, 0.756, and 0.889, respectively). Finally, a Cox regression model also identified beta-IGH3 as an independent prognostic factor (P=0.01). CONCLUSION: Beta-IGH3 is highly expressed in lung cancers and may be a potential target for lung cancer treatments. Dove Medical Press 2016-08-11 /pmc/articles/PMC4986675/ /pubmed/27563252 http://dx.doi.org/10.2147/OTT.S100102 Text en © 2016 He et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research He, Changjun Sun, Dawei Bai, Xue Li, Yingbin Xu, Hai Xu, Shidong Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
title | Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
title_full | Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
title_fullStr | Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
title_full_unstemmed | Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
title_short | Clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
title_sort | clinical implications of transforming growth factor-beta–induced gene-h3 protein expression in lung cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986675/ https://www.ncbi.nlm.nih.gov/pubmed/27563252 http://dx.doi.org/10.2147/OTT.S100102 |
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