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NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer

PURPOSE: This study aimed to investigate the effect of NPTX1 on the prognosis of gastric cancer (GC), as well as the metastatic process in GC. MATERIALS AND METHODS: The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases were used to analyze the association between NPTX1 expressi...

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Autores principales: Yan, Hongfei, Zheng, Chunlei, Li, Zhi, Bao, Bowen, Yang, Bowen, Hou, Kezuo, Qu, Xiujuan, Xiao, Jiawen, Che, Xiaofang, Liu, Yunpeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472287/
https://www.ncbi.nlm.nih.gov/pubmed/31043800
http://dx.doi.org/10.2147/CMAR.S196509
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author Yan, Hongfei
Zheng, Chunlei
Li, Zhi
Bao, Bowen
Yang, Bowen
Hou, Kezuo
Qu, Xiujuan
Xiao, Jiawen
Che, Xiaofang
Liu, Yunpeng
author_facet Yan, Hongfei
Zheng, Chunlei
Li, Zhi
Bao, Bowen
Yang, Bowen
Hou, Kezuo
Qu, Xiujuan
Xiao, Jiawen
Che, Xiaofang
Liu, Yunpeng
author_sort Yan, Hongfei
collection PubMed
description PURPOSE: This study aimed to investigate the effect of NPTX1 on the prognosis of gastric cancer (GC), as well as the metastatic process in GC. MATERIALS AND METHODS: The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases were used to analyze the association between NPTX1 expression and prognosis in GC. Quantitative real-time polymerase chain reaction and Western blots were applied to examine the expression of NPTX1 in GC cell lines and expression of genes in downstream pathways. The role of NPTX1 on the migration, invasion, adhesion, and proliferation of GC cell lines was investigated with the transwell assay, the adhesion assay, and the MTT assay. Immunofluorescence staining was used to observe the effect of NPTX1 knockdown on the morphology of cells. RESULTS: According to the review of TCGA and GEO databases of GC, we found that the expression of NPTX1 increased in cancer tissues and high NPTX1 expression was correlated with poor overall survival, which was associated with lymph node stage in clinicopathologic parameters. Knockdown of NPTX1 attenuated the migration, invasion, and adhesion abilities of GC cells. According to gene set enrichment analysis, NPTX1 was found to be positively related to integrin and focal adhesion (FA). Additionally, NPTX1 knockdown decreased the expression of integrin α1 and integrin α7, followed by deregulation of the expression of p-Src, p-Akt, p-Erk, MMP2, and MMP7, as well as inhibiting the formation of FA complexes and decreasing the length of pseudopods in GC cells. CONCLUSION: Our study provides strong evidence that NPTX1 plays a crucial role in promoting metastasis and acts as a prognostic indicator in GC.
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spelling pubmed-64722872019-05-01 NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer Yan, Hongfei Zheng, Chunlei Li, Zhi Bao, Bowen Yang, Bowen Hou, Kezuo Qu, Xiujuan Xiao, Jiawen Che, Xiaofang Liu, Yunpeng Cancer Manag Res Original Research PURPOSE: This study aimed to investigate the effect of NPTX1 on the prognosis of gastric cancer (GC), as well as the metastatic process in GC. MATERIALS AND METHODS: The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases were used to analyze the association between NPTX1 expression and prognosis in GC. Quantitative real-time polymerase chain reaction and Western blots were applied to examine the expression of NPTX1 in GC cell lines and expression of genes in downstream pathways. The role of NPTX1 on the migration, invasion, adhesion, and proliferation of GC cell lines was investigated with the transwell assay, the adhesion assay, and the MTT assay. Immunofluorescence staining was used to observe the effect of NPTX1 knockdown on the morphology of cells. RESULTS: According to the review of TCGA and GEO databases of GC, we found that the expression of NPTX1 increased in cancer tissues and high NPTX1 expression was correlated with poor overall survival, which was associated with lymph node stage in clinicopathologic parameters. Knockdown of NPTX1 attenuated the migration, invasion, and adhesion abilities of GC cells. According to gene set enrichment analysis, NPTX1 was found to be positively related to integrin and focal adhesion (FA). Additionally, NPTX1 knockdown decreased the expression of integrin α1 and integrin α7, followed by deregulation of the expression of p-Src, p-Akt, p-Erk, MMP2, and MMP7, as well as inhibiting the formation of FA complexes and decreasing the length of pseudopods in GC cells. CONCLUSION: Our study provides strong evidence that NPTX1 plays a crucial role in promoting metastasis and acts as a prognostic indicator in GC. Dove Medical Press 2019-04-15 /pmc/articles/PMC6472287/ /pubmed/31043800 http://dx.doi.org/10.2147/CMAR.S196509 Text en © 2019 Yan 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
Yan, Hongfei
Zheng, Chunlei
Li, Zhi
Bao, Bowen
Yang, Bowen
Hou, Kezuo
Qu, Xiujuan
Xiao, Jiawen
Che, Xiaofang
Liu, Yunpeng
NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer
title NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer
title_full NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer
title_fullStr NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer
title_full_unstemmed NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer
title_short NPTX1 promotes metastasis via integrin/FAK signaling in gastric cancer
title_sort nptx1 promotes metastasis via integrin/fak signaling in gastric cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472287/
https://www.ncbi.nlm.nih.gov/pubmed/31043800
http://dx.doi.org/10.2147/CMAR.S196509
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