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Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer

The aim of the present study was to investigate the expression levels of transforming growth factor-β (TGF-β) receptor type II (TβRII) and DPC4/Smad4 in the TGF-β signaling pathway and the importance of these expression levels in non-small cell lung cancer (NSCLC). The mRNA and protein expression le...

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Autores principales: CHEN, HONG, WANG, JING-WEI, LIU, LI-XIN, YAN, JI-DONG, REN, SHU-HUA, LI, YAN, LU, ZHENG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247285/
https://www.ncbi.nlm.nih.gov/pubmed/25452807
http://dx.doi.org/10.3892/etm.2014.2065
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author CHEN, HONG
WANG, JING-WEI
LIU, LI-XIN
YAN, JI-DONG
REN, SHU-HUA
LI, YAN
LU, ZHENG
author_facet CHEN, HONG
WANG, JING-WEI
LIU, LI-XIN
YAN, JI-DONG
REN, SHU-HUA
LI, YAN
LU, ZHENG
author_sort CHEN, HONG
collection PubMed
description The aim of the present study was to investigate the expression levels of transforming growth factor-β (TGF-β) receptor type II (TβRII) and DPC4/Smad4 in the TGF-β signaling pathway and the importance of these expression levels in non-small cell lung cancer (NSCLC). The mRNA and protein expression levels of TβRII and DPC4/Smad4 were detected by reverse transcription-quantitative polymerase chain reaction and western blotting, respectively, in NSCLC and control nonlesional lung tissues of 60 patients. The protein expression levels of DPC4/Smad4 were detected by immunohistochemistry in paraffin-embedded samples of NSCLC. In addition, the correlations among the expression levels of TβRII and DPC4/Smad4 and their association with the clinical and pathological features of NSCLC were analyzed. The expression levels of TβRII and DPC4/Smad4 in NSCLC tissues were significantly lower when compared with the control nonlesional lung tissues (P<0.05). In addition, the expression of TβRII and DPC4/Smad4 in poorly-differentiated NSCLC tissues was significantly lower compared with moderately- or well-differentiated NSCLC tissues (P<0.05). The expression levels of TβRII and DPC4/Smad4 were significantly lower in NSCLC tissues with metastatic lymph nodes compared with tissue without metastatic lymph nodes (P<0.05). Thus, the expression levels were demonstrated to significantly correlate with the clinical and pathological stages, and subsequently were shown to be associated with the occurrence and progression of NSCLC. In conclusion, TβRII and DPC4/Smad4 may play an important role in the tumorigenesis, differentiation and progression of NSCLC via the TGF-β signaling pathway.
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spelling pubmed-42472852014-12-01 Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer CHEN, HONG WANG, JING-WEI LIU, LI-XIN YAN, JI-DONG REN, SHU-HUA LI, YAN LU, ZHENG Exp Ther Med Articles The aim of the present study was to investigate the expression levels of transforming growth factor-β (TGF-β) receptor type II (TβRII) and DPC4/Smad4 in the TGF-β signaling pathway and the importance of these expression levels in non-small cell lung cancer (NSCLC). The mRNA and protein expression levels of TβRII and DPC4/Smad4 were detected by reverse transcription-quantitative polymerase chain reaction and western blotting, respectively, in NSCLC and control nonlesional lung tissues of 60 patients. The protein expression levels of DPC4/Smad4 were detected by immunohistochemistry in paraffin-embedded samples of NSCLC. In addition, the correlations among the expression levels of TβRII and DPC4/Smad4 and their association with the clinical and pathological features of NSCLC were analyzed. The expression levels of TβRII and DPC4/Smad4 in NSCLC tissues were significantly lower when compared with the control nonlesional lung tissues (P<0.05). In addition, the expression of TβRII and DPC4/Smad4 in poorly-differentiated NSCLC tissues was significantly lower compared with moderately- or well-differentiated NSCLC tissues (P<0.05). The expression levels of TβRII and DPC4/Smad4 were significantly lower in NSCLC tissues with metastatic lymph nodes compared with tissue without metastatic lymph nodes (P<0.05). Thus, the expression levels were demonstrated to significantly correlate with the clinical and pathological stages, and subsequently were shown to be associated with the occurrence and progression of NSCLC. In conclusion, TβRII and DPC4/Smad4 may play an important role in the tumorigenesis, differentiation and progression of NSCLC via the TGF-β signaling pathway. D.A. Spandidos 2015-01 2014-11-12 /pmc/articles/PMC4247285/ /pubmed/25452807 http://dx.doi.org/10.3892/etm.2014.2065 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
CHEN, HONG
WANG, JING-WEI
LIU, LI-XIN
YAN, JI-DONG
REN, SHU-HUA
LI, YAN
LU, ZHENG
Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer
title Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer
title_full Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer
title_fullStr Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer
title_full_unstemmed Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer
title_short Expression and significance of transforming growth factor-β receptor type II and DPC4/Smad4 in non-small cell lung cancer
title_sort expression and significance of transforming growth factor-β receptor type ii and dpc4/smad4 in non-small cell lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247285/
https://www.ncbi.nlm.nih.gov/pubmed/25452807
http://dx.doi.org/10.3892/etm.2014.2065
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