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Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination

BACKGROUND: Connective tissue growth factor (CTGF) has been shown to be implicated in tumor development and progression. However, the role of CTGF in gastric cancer remains largely unknown. RESULTS: In this study, we showed that CTGF was highly expressed in gastric cancer tissues compared with match...

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Autores principales: Jiang, Cheng-Gang, Lv, Ling, Liu, Fu-Rong, Wang, Zhen-Ning, Liu, Fu-Nan, Li, Yan-Shu, Wang, Chun-Yu, Zhang, Hong-Yan, Sun, Zhe, Xu, Hui-Mian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192775/
https://www.ncbi.nlm.nih.gov/pubmed/21955589
http://dx.doi.org/10.1186/1476-4598-10-122
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author Jiang, Cheng-Gang
Lv, Ling
Liu, Fu-Rong
Wang, Zhen-Ning
Liu, Fu-Nan
Li, Yan-Shu
Wang, Chun-Yu
Zhang, Hong-Yan
Sun, Zhe
Xu, Hui-Mian
author_facet Jiang, Cheng-Gang
Lv, Ling
Liu, Fu-Rong
Wang, Zhen-Ning
Liu, Fu-Nan
Li, Yan-Shu
Wang, Chun-Yu
Zhang, Hong-Yan
Sun, Zhe
Xu, Hui-Mian
author_sort Jiang, Cheng-Gang
collection PubMed
description BACKGROUND: Connective tissue growth factor (CTGF) has been shown to be implicated in tumor development and progression. However, the role of CTGF in gastric cancer remains largely unknown. RESULTS: In this study, we showed that CTGF was highly expressed in gastric cancer tissues compared with matched normal gastric tissues. The CTGF expression in tumor tissue was associated with histologic grade, lymph node metastasis and peritoneal dissemination (P < 0.05). Patients with positive CTGF expression had significantly lower cumulative postoperative 5 year survival rate than those with negative CTGF expression (22.9% versus 48.1%, P < 0.001). We demonstrated that knockdown of CTGF expression significantly inhibited cell growth of gastric cancer cells and decreased cyclin D(1 )expression. Moreover, knockdown of CTGF expression also markedly reduced the migration and invasion of gastric cancer cells and decreased the expression of matrix metalloproteinase (MMP)-2 and MMP-9. Animal studies revealed that nude mice injected with the CTGF knockdown stable cell lines featured a smaller number of peritoneal seeding nodules than the control cell lines. CONCLUSIONS: These data suggest that CTGF plays an important role in cell growth and invasion in human gastric cancer and it appears to be a potential prognostic marker for patients with gastric cancer.
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spelling pubmed-31927752011-10-14 Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination Jiang, Cheng-Gang Lv, Ling Liu, Fu-Rong Wang, Zhen-Ning Liu, Fu-Nan Li, Yan-Shu Wang, Chun-Yu Zhang, Hong-Yan Sun, Zhe Xu, Hui-Mian Mol Cancer Research BACKGROUND: Connective tissue growth factor (CTGF) has been shown to be implicated in tumor development and progression. However, the role of CTGF in gastric cancer remains largely unknown. RESULTS: In this study, we showed that CTGF was highly expressed in gastric cancer tissues compared with matched normal gastric tissues. The CTGF expression in tumor tissue was associated with histologic grade, lymph node metastasis and peritoneal dissemination (P < 0.05). Patients with positive CTGF expression had significantly lower cumulative postoperative 5 year survival rate than those with negative CTGF expression (22.9% versus 48.1%, P < 0.001). We demonstrated that knockdown of CTGF expression significantly inhibited cell growth of gastric cancer cells and decreased cyclin D(1 )expression. Moreover, knockdown of CTGF expression also markedly reduced the migration and invasion of gastric cancer cells and decreased the expression of matrix metalloproteinase (MMP)-2 and MMP-9. Animal studies revealed that nude mice injected with the CTGF knockdown stable cell lines featured a smaller number of peritoneal seeding nodules than the control cell lines. CONCLUSIONS: These data suggest that CTGF plays an important role in cell growth and invasion in human gastric cancer and it appears to be a potential prognostic marker for patients with gastric cancer. BioMed Central 2011-09-28 /pmc/articles/PMC3192775/ /pubmed/21955589 http://dx.doi.org/10.1186/1476-4598-10-122 Text en Copyright ©2011 Jiang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Jiang, Cheng-Gang
Lv, Ling
Liu, Fu-Rong
Wang, Zhen-Ning
Liu, Fu-Nan
Li, Yan-Shu
Wang, Chun-Yu
Zhang, Hong-Yan
Sun, Zhe
Xu, Hui-Mian
Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
title Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
title_full Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
title_fullStr Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
title_full_unstemmed Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
title_short Downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
title_sort downregulation of connective tissue growth factor inhibits the growth and invasion of gastric cancer cells and attenuates peritoneal dissemination
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192775/
https://www.ncbi.nlm.nih.gov/pubmed/21955589
http://dx.doi.org/10.1186/1476-4598-10-122
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