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AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression

The LIM-domain protein AJUBA has been reported to be involved in cell-cell adhesion, proliferation, migration and cell fate decision by acting as a scaffold or adaptor protein. We previously identified AJUBA as a putative cancer gene in esophageal squamous cell carcinoma (ESCC). However, the functio...

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Autores principales: Shi, Xuejiao, Chen, Zhaoli, Hu, Xueda, Luo, Mei, Sun, Zengmiao, Li, Jiagen, Shi, Susheng, Feng, Xiaoli, Zhou, Chengcheng, Li, Zitong, Yang, Wenhui, Li, Yuan, Wang, Pan, Zhou, Fang, Gao, Yibo, He, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095009/
https://www.ncbi.nlm.nih.gov/pubmed/27172796
http://dx.doi.org/10.18632/oncotarget.9239
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author Shi, Xuejiao
Chen, Zhaoli
Hu, Xueda
Luo, Mei
Sun, Zengmiao
Li, Jiagen
Shi, Susheng
Feng, Xiaoli
Zhou, Chengcheng
Li, Zitong
Yang, Wenhui
Li, Yuan
Wang, Pan
Zhou, Fang
Gao, Yibo
He, Jie
author_facet Shi, Xuejiao
Chen, Zhaoli
Hu, Xueda
Luo, Mei
Sun, Zengmiao
Li, Jiagen
Shi, Susheng
Feng, Xiaoli
Zhou, Chengcheng
Li, Zitong
Yang, Wenhui
Li, Yuan
Wang, Pan
Zhou, Fang
Gao, Yibo
He, Jie
author_sort Shi, Xuejiao
collection PubMed
description The LIM-domain protein AJUBA has been reported to be involved in cell-cell adhesion, proliferation, migration and cell fate decision by acting as a scaffold or adaptor protein. We previously identified AJUBA as a putative cancer gene in esophageal squamous cell carcinoma (ESCC). However, the function and underlying mechanisms of AJUBA in ESCC remain largely unknown. In the present study, we detected AJUBA levels in ESCC tumor tissues and in corresponding adjacent non-tumor tissues by immunohistochemistry (IHC) and investigated the function and mechanism of AJUBA in ESCC cells. The IHC results showed that AJUBA levels were significantly higher in ESCC tissues compared with corresponding adjacent non-tumor tissues (P < 0.001). Both in vitro and in vivo experiments showed that AJUBA promoted cell growth and colony formation, inhibited cisplatin-induced apoptosis of ESCC cells, and promoted ESCC cell migration and invasion. RNA sequencing was used to reveal the oncogenic pathways of AJUBA that were involved, and MMP10 and MMP13 were identified as two of the downstream targets of AJUBA. Thus, AJUBA upregulates the levels of MMP10 and MMP13 by activating ERK1/2. Taken together, these findings revealed that AJUBA serves as oncogenic gene in ESCC and may serve as a new target for ESCC therapy.
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spelling pubmed-50950092016-11-22 AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression Shi, Xuejiao Chen, Zhaoli Hu, Xueda Luo, Mei Sun, Zengmiao Li, Jiagen Shi, Susheng Feng, Xiaoli Zhou, Chengcheng Li, Zitong Yang, Wenhui Li, Yuan Wang, Pan Zhou, Fang Gao, Yibo He, Jie Oncotarget Research Paper The LIM-domain protein AJUBA has been reported to be involved in cell-cell adhesion, proliferation, migration and cell fate decision by acting as a scaffold or adaptor protein. We previously identified AJUBA as a putative cancer gene in esophageal squamous cell carcinoma (ESCC). However, the function and underlying mechanisms of AJUBA in ESCC remain largely unknown. In the present study, we detected AJUBA levels in ESCC tumor tissues and in corresponding adjacent non-tumor tissues by immunohistochemistry (IHC) and investigated the function and mechanism of AJUBA in ESCC cells. The IHC results showed that AJUBA levels were significantly higher in ESCC tissues compared with corresponding adjacent non-tumor tissues (P < 0.001). Both in vitro and in vivo experiments showed that AJUBA promoted cell growth and colony formation, inhibited cisplatin-induced apoptosis of ESCC cells, and promoted ESCC cell migration and invasion. RNA sequencing was used to reveal the oncogenic pathways of AJUBA that were involved, and MMP10 and MMP13 were identified as two of the downstream targets of AJUBA. Thus, AJUBA upregulates the levels of MMP10 and MMP13 by activating ERK1/2. Taken together, these findings revealed that AJUBA serves as oncogenic gene in ESCC and may serve as a new target for ESCC therapy. Impact Journals LLC 2016-05-09 /pmc/articles/PMC5095009/ /pubmed/27172796 http://dx.doi.org/10.18632/oncotarget.9239 Text en Copyright: © 2016 Shi et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Shi, Xuejiao
Chen, Zhaoli
Hu, Xueda
Luo, Mei
Sun, Zengmiao
Li, Jiagen
Shi, Susheng
Feng, Xiaoli
Zhou, Chengcheng
Li, Zitong
Yang, Wenhui
Li, Yuan
Wang, Pan
Zhou, Fang
Gao, Yibo
He, Jie
AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression
title AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression
title_full AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression
title_fullStr AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression
title_full_unstemmed AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression
title_short AJUBA promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of MMP10 and MMP13 expression
title_sort ajuba promotes the migration and invasion of esophageal squamous cell carcinoma cells through upregulation of mmp10 and mmp13 expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095009/
https://www.ncbi.nlm.nih.gov/pubmed/27172796
http://dx.doi.org/10.18632/oncotarget.9239
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