Academic Journal

The role of sentrin-specific protease 2 substrate recognition in TGF-β-induced tumorigenesis

التفاصيل البيبلوغرافية
العنوان: The role of sentrin-specific protease 2 substrate recognition in TGF-β-induced tumorigenesis
المؤلفون: Chang, Che-Chang, Huang, Yen-Sung, Lin, Ying-Mei, Lin, Chia-Ju, Jeng, Jen-Chong, Liu, Shin-Mei, Ho, Tsai-Ling, Chang, Ruei-Ting, Changou, Chun A., Ho, Chun-Chen, Shih, Hsiu-Ming
المساهمون: Ministry of Science and Technology, Taiwan
المصدر: Scientific Reports ; volume 8, issue 1 ; ISSN 2045-2322
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2018
الوصف: Smad4, a common-mediator of Smads, plays a central role in forming complexes with receptor-phosphorylated Smads, and then transduces transforming growth factor (TGF)-β signals into the nuclei. Although many cellular factors are involved in TGF-β induced epithelial-to-mesenchymal transition (EMT) and cell migration, very little is known with the mechanism of Smad4 regulation on pro-oncogenes response by TGF-β. Herein, we demonstrate the interaction of Sentrin-specific protease 2 (SENP2) with Smad4 through SENP2 residue 363~400. The same segment is also important for desumoylation of Smad4, and able to relieve sumoylation-mediated TGF-β repression. The SENP2 363~400 segment is critical for TGF-β-induced cell migration, which is correlated with SENP2 363~400 deletion mutant failed to increase matrix metalloproteinase (MMP)-9 and EMT marker gene expression. Moreover, our results suggest that the interaction and desumoylation between SENP2 and Smad4 promote cell migration in triple-negative breast cancer cells. Altogether, our data show how SENP2 regulates its substrate for desumoylation, and also the role of SENP2 in TGF-β induced cancer cell migration.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1038/s41598-018-28103-8
الاتاحة: http://dx.doi.org/10.1038/s41598-018-28103-8
https://www.nature.com/articles/s41598-018-28103-8.pdf
https://www.nature.com/articles/s41598-018-28103-8
Rights: https://creativecommons.org/licenses/by/4.0 ; https://creativecommons.org/licenses/by/4.0
رقم الانضمام: edsbas.65C071BB
قاعدة البيانات: BASE
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