C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells

Abstract Complement component 1q subcomponent binding protein (C1QBP) is a ubiquitously expressed cellular protein and can be upregulated or activated in a variety of malignant tumors, including those from thyroid, colon and breast, but its role remains unclear in renal cell carcinoma (RCC). In this...

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Main Authors: Yong Wang, Donghe Fu, Jing Su, Yajing Chen, Can Qi, Yin Sun, Yuanjie Niu, Ning Zhang, Dan Yue
Format: Article
Language:English
Published: Nature Publishing Group 2017-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-01084-w
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spelling doaj-178b5436c2484fa38bb8ff14981b02e42020-12-08T03:05:10ZengNature Publishing GroupScientific Reports2045-23222017-04-01711910.1038/s41598-017-01084-wC1QBP suppresses cell adhesion and metastasis of renal carcinoma cellsYong Wang0Donghe Fu1Jing Su2Yajing Chen3Can Qi4Yin Sun5Yuanjie Niu6Ning Zhang7Dan Yue8Department of Urology, Tianjin Medical University Second Hospital, Tianjin Institute of Urology, Tianjin Medical UniversitySchool of Laboratory Medicine, Tianjin Medical UniversitySchool of Laboratory Medicine, Tianjin Medical UniversitySchool of Laboratory Medicine, Tianjin Medical UniversityDepartment of Urology, Children’s Hospital of Hebei ProvinceDepartment of Radiation Oncology, University of Rochester Medical CenterDepartment of Urology, Tianjin Medical University Second Hospital, Tianjin Institute of Urology, Tianjin Medical UniversityTianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Research Center of Basic Medical SciencesSchool of Laboratory Medicine, Tianjin Medical UniversityAbstract Complement component 1q subcomponent binding protein (C1QBP) is a ubiquitously expressed cellular protein and can be upregulated or activated in a variety of malignant tumors, including those from thyroid, colon and breast, but its role remains unclear in renal cell carcinoma (RCC). In this study, C1QBP knockdown in RCC cell influenced expression of multiple genes associated with cell adhesion, among which L1 cell adhesion molecule (L1CAM) was significantly higher upon a reduction of C1QBP. In turn, cell adhesion and invasion abilities were significantly increased with increased metastasis to lung and liver in vivo. C1QBP may regulate RCC cell adhesion and invasion through influencing the p-GSK3/β-Catenin/L1CAM expression. Over all, our study demonstrated that C1QBP could regulate RCC metastasis by regulating the GSK3/β-Catenin/L1CAM signaling pathway.https://doi.org/10.1038/s41598-017-01084-w
collection DOAJ
language English
format Article
sources DOAJ
author Yong Wang
Donghe Fu
Jing Su
Yajing Chen
Can Qi
Yin Sun
Yuanjie Niu
Ning Zhang
Dan Yue
spellingShingle Yong Wang
Donghe Fu
Jing Su
Yajing Chen
Can Qi
Yin Sun
Yuanjie Niu
Ning Zhang
Dan Yue
C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells
Scientific Reports
author_facet Yong Wang
Donghe Fu
Jing Su
Yajing Chen
Can Qi
Yin Sun
Yuanjie Niu
Ning Zhang
Dan Yue
author_sort Yong Wang
title C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells
title_short C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells
title_full C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells
title_fullStr C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells
title_full_unstemmed C1QBP suppresses cell adhesion and metastasis of renal carcinoma cells
title_sort c1qbp suppresses cell adhesion and metastasis of renal carcinoma cells
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-04-01
description Abstract Complement component 1q subcomponent binding protein (C1QBP) is a ubiquitously expressed cellular protein and can be upregulated or activated in a variety of malignant tumors, including those from thyroid, colon and breast, but its role remains unclear in renal cell carcinoma (RCC). In this study, C1QBP knockdown in RCC cell influenced expression of multiple genes associated with cell adhesion, among which L1 cell adhesion molecule (L1CAM) was significantly higher upon a reduction of C1QBP. In turn, cell adhesion and invasion abilities were significantly increased with increased metastasis to lung and liver in vivo. C1QBP may regulate RCC cell adhesion and invasion through influencing the p-GSK3/β-Catenin/L1CAM expression. Over all, our study demonstrated that C1QBP could regulate RCC metastasis by regulating the GSK3/β-Catenin/L1CAM signaling pathway.
url https://doi.org/10.1038/s41598-017-01084-w
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