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The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma

The tetraspanin KAI1/CD82 was identified as a tumor metastasis suppressor that downregulated in various malignant cell types. However, the function of CD82 and its underlying anti-metastasis role in renal cell carcinoma (RCC) is still unraveled. Here, we investigated the expression of CD82 in RCC an...

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Autores principales: Zhu, Jundong, Liang, Chao, Hua, Yibo, Miao, Chenkui, Zhang, Jianzhong, Xu, Aiming, Zhao, Kai, Liu, Shouyong, Tian, Ye, Dong, Huiyu, Zhang, Chao, Li, Pu, Su, Shifeng, Qin, Chao, Wang, Zengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584269/
https://www.ncbi.nlm.nih.gov/pubmed/28881668
http://dx.doi.org/10.18632/oncotarget.18086
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author Zhu, Jundong
Liang, Chao
Hua, Yibo
Miao, Chenkui
Zhang, Jianzhong
Xu, Aiming
Zhao, Kai
Liu, Shouyong
Tian, Ye
Dong, Huiyu
Zhang, Chao
Li, Pu
Su, Shifeng
Qin, Chao
Wang, Zengjun
author_facet Zhu, Jundong
Liang, Chao
Hua, Yibo
Miao, Chenkui
Zhang, Jianzhong
Xu, Aiming
Zhao, Kai
Liu, Shouyong
Tian, Ye
Dong, Huiyu
Zhang, Chao
Li, Pu
Su, Shifeng
Qin, Chao
Wang, Zengjun
author_sort Zhu, Jundong
collection PubMed
description The tetraspanin KAI1/CD82 was identified as a tumor metastasis suppressor that downregulated in various malignant cell types. However, the function of CD82 and its underlying anti-metastasis role in renal cell carcinoma (RCC) is still unraveled. Here, we investigated the expression of CD82 in RCC and explored its regulatory mechanism in RCC cell lines. We found that CD82 was down-regulated in RCC tissues and cells and its expression was significantly associated with histological grade(p=0.041), tumour stage (p=0.036) and tumor size(p=0.020) by analyzing tissue microarrays. After upregulation of CD82 through lentivirus, reduced ability of migration and invasion in Caki-1 cells were detected. In contrast, gene silencing of CD82 by small interfering RNA promoted metastatic and invasive potential of 786-O cells. Furthermore, Western blot was performed to identify the influence of CD82 on MMP family and TGF-β1/Smad pathway in RCC. Subsequently, upregulating protein level of TGF-β1 with the overexpression of CD82 could rescue the malignant behaviors inhibited by CD82 which indicated that CD82 played its inhibitory role in RCC partially by attenuating the expression of TGF-β1. Taken together, CD82 played a prominent role in migration and invasion of RCC cells and it might exhibit its inhibitory role in RCC metastasis via block TGF-β1/Smad signaling pathway.
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spelling pubmed-55842692017-09-06 The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma Zhu, Jundong Liang, Chao Hua, Yibo Miao, Chenkui Zhang, Jianzhong Xu, Aiming Zhao, Kai Liu, Shouyong Tian, Ye Dong, Huiyu Zhang, Chao Li, Pu Su, Shifeng Qin, Chao Wang, Zengjun Oncotarget Research Paper The tetraspanin KAI1/CD82 was identified as a tumor metastasis suppressor that downregulated in various malignant cell types. However, the function of CD82 and its underlying anti-metastasis role in renal cell carcinoma (RCC) is still unraveled. Here, we investigated the expression of CD82 in RCC and explored its regulatory mechanism in RCC cell lines. We found that CD82 was down-regulated in RCC tissues and cells and its expression was significantly associated with histological grade(p=0.041), tumour stage (p=0.036) and tumor size(p=0.020) by analyzing tissue microarrays. After upregulation of CD82 through lentivirus, reduced ability of migration and invasion in Caki-1 cells were detected. In contrast, gene silencing of CD82 by small interfering RNA promoted metastatic and invasive potential of 786-O cells. Furthermore, Western blot was performed to identify the influence of CD82 on MMP family and TGF-β1/Smad pathway in RCC. Subsequently, upregulating protein level of TGF-β1 with the overexpression of CD82 could rescue the malignant behaviors inhibited by CD82 which indicated that CD82 played its inhibitory role in RCC partially by attenuating the expression of TGF-β1. Taken together, CD82 played a prominent role in migration and invasion of RCC cells and it might exhibit its inhibitory role in RCC metastasis via block TGF-β1/Smad signaling pathway. Impact Journals LLC 2017-05-23 /pmc/articles/PMC5584269/ /pubmed/28881668 http://dx.doi.org/10.18632/oncotarget.18086 Text en Copyright: © 2017 Zhu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhu, Jundong
Liang, Chao
Hua, Yibo
Miao, Chenkui
Zhang, Jianzhong
Xu, Aiming
Zhao, Kai
Liu, Shouyong
Tian, Ye
Dong, Huiyu
Zhang, Chao
Li, Pu
Su, Shifeng
Qin, Chao
Wang, Zengjun
The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma
title The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma
title_full The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma
title_fullStr The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma
title_full_unstemmed The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma
title_short The metastasis suppressor CD82/KAI1 regulates cell migration and invasion via inhibiting TGF-β 1/Smad signaling in renal cell carcinoma
title_sort metastasis suppressor cd82/kai1 regulates cell migration and invasion via inhibiting tgf-β 1/smad signaling in renal cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584269/
https://www.ncbi.nlm.nih.gov/pubmed/28881668
http://dx.doi.org/10.18632/oncotarget.18086
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