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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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 |
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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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