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The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling
Renal cell carcinoma (RCC) is a common kidney cancer worldwide. Even though current treatments show promising therapeutic effectiveness, metastatic RCC still has limited therapeutic options so that novel treatments were urgently needed. Here, we identified that MUC12 was overexpressed in RCC patient...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412406/ https://www.ncbi.nlm.nih.gov/pubmed/32596961 http://dx.doi.org/10.1111/jcmm.15515 |
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author | Gao, Sheng‐Lin Yin, Rui Zhang, Li‐Feng Wang, Si‐Min Chen, Jia‐Sheng Wu, Xing‐Yu Yue, Chuang Zuo, Li Tang, Min |
author_facet | Gao, Sheng‐Lin Yin, Rui Zhang, Li‐Feng Wang, Si‐Min Chen, Jia‐Sheng Wu, Xing‐Yu Yue, Chuang Zuo, Li Tang, Min |
author_sort | Gao, Sheng‐Lin |
collection | PubMed |
description | Renal cell carcinoma (RCC) is a common kidney cancer worldwide. Even though current treatments show promising therapeutic effectiveness, metastatic RCC still has limited therapeutic options so that novel treatments were urgently needed. Here, we identified that MUC12 was overexpressed in RCC patients and served as poor prognostic factor for RCC progression. Overexpression of MUC12 increased RCC cell growth and cell invasion while deficiency of MUC12 exerted opposite effects on RCC cells. Mechanistic dissection demonstrated that MUC12‐mediated RCC cell growth and cell invasion were dependent of TGF‐β1 signalling because they could be blocked in the presence of TGF‐β1 inhibitor. Moreover, the regulation of TGF‐β1 by MUC12 relied on the transactivation of c‐Jun. MUC12 promoted the recruitment of c‐Jun on the promoter of TGF‐β1, leading to its transcription. Importantly, knockdown of c‐Jun also attenuated MUC12‐mediated TGF‐β1 induction and RCC cell invasion. In summary, our study defines the role of MUC12 in RCC progression and provides rational to develop novel targeted therapy to battle against RCC. |
format | Online Article Text |
id | pubmed-7412406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74124062020-08-10 The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling Gao, Sheng‐Lin Yin, Rui Zhang, Li‐Feng Wang, Si‐Min Chen, Jia‐Sheng Wu, Xing‐Yu Yue, Chuang Zuo, Li Tang, Min J Cell Mol Med Original Articles Renal cell carcinoma (RCC) is a common kidney cancer worldwide. Even though current treatments show promising therapeutic effectiveness, metastatic RCC still has limited therapeutic options so that novel treatments were urgently needed. Here, we identified that MUC12 was overexpressed in RCC patients and served as poor prognostic factor for RCC progression. Overexpression of MUC12 increased RCC cell growth and cell invasion while deficiency of MUC12 exerted opposite effects on RCC cells. Mechanistic dissection demonstrated that MUC12‐mediated RCC cell growth and cell invasion were dependent of TGF‐β1 signalling because they could be blocked in the presence of TGF‐β1 inhibitor. Moreover, the regulation of TGF‐β1 by MUC12 relied on the transactivation of c‐Jun. MUC12 promoted the recruitment of c‐Jun on the promoter of TGF‐β1, leading to its transcription. Importantly, knockdown of c‐Jun also attenuated MUC12‐mediated TGF‐β1 induction and RCC cell invasion. In summary, our study defines the role of MUC12 in RCC progression and provides rational to develop novel targeted therapy to battle against RCC. John Wiley and Sons Inc. 2020-06-28 2020-08 /pmc/articles/PMC7412406/ /pubmed/32596961 http://dx.doi.org/10.1111/jcmm.15515 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Gao, Sheng‐Lin Yin, Rui Zhang, Li‐Feng Wang, Si‐Min Chen, Jia‐Sheng Wu, Xing‐Yu Yue, Chuang Zuo, Li Tang, Min The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling |
title | The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling |
title_full | The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling |
title_fullStr | The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling |
title_full_unstemmed | The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling |
title_short | The oncogenic role of MUC12 in RCC progression depends on c‐Jun/TGF‐β signalling |
title_sort | oncogenic role of muc12 in rcc progression depends on c‐jun/tgf‐β signalling |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412406/ https://www.ncbi.nlm.nih.gov/pubmed/32596961 http://dx.doi.org/10.1111/jcmm.15515 |
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