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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...

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Autores principales: He, Changjun, Sun, Dawei, Bai, Xue, Li, Yingbin, Xu, Hai, Xu, Shidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
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.
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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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