Academic Journal
Smad Ubiquitination Regulatory Factor 1 (Smurf1) Promotes Thyroid Cancer Cell Proliferation and Migration via Ubiquitin-Dependent Degradation of Kisspeptin-1
العنوان: | Smad Ubiquitination Regulatory Factor 1 (Smurf1) Promotes Thyroid Cancer Cell Proliferation and Migration via Ubiquitin-Dependent Degradation of Kisspeptin-1 |
---|---|
المؤلفون: | Chunyan Yan, Haiying Su, Xiyuan Song, Huiling Cao, Lingling Kong, Wen Cui |
المصدر: | Cellular Physiology and Biochemistry, Vol 49, Iss 5, Pp 2047-2059 (2018) |
بيانات النشر: | Cell Physiol Biochem Press GmbH & Co KG, 2018. |
سنة النشر: | 2018 |
المجموعة: | LCC:Physiology LCC:Biochemistry |
مصطلحات موضوعية: | Thyroid cancer, Smad ubiquitination regulatory factor 1, Kisspeptin-1, Ubiquitin-dependent degradation, NF-κB signaling pathway, Physiology, QP1-981, Biochemistry, QD415-436 |
الوصف: | Background/Aims: Thyroid cancer is the most common malignancy in human endocrine system. Smad ubiquitination regulatory factor 1 (Smurf1) is an E3 ubiquitin-protein ligase in ubiquitin-proteasome pathway (UPP) system. This study aimed to investigate the effects of Smurf1 on thyroid cancer proliferation and metastasis, as well as underlying potential mechanism. Methods: The expression levels of Smurf1 in thyroid tumor tissues and thyroid cancer cells were detected by western blotting and qRT-PCR. Then, the effects of up-regulation or down-regulation of Smurf1 on thyroid cancer cell viability, migration, invasion, proliferation and apoptosis were measured using trypan blue exclusion assay, two-chamber migration (invasion) assay, cell colony formation assay and Guava Nexin assay, respectively. The ubiquitination of kisspeptin-1 (KISS-1) was assessed by protein ubiquitination assay. Finally, the effects of KISS-1 overexpression on activity of nuclear factor-kappa B (NF-κB) signaling pathway, as well as thyroid cancer cell viability, migration, invasion, proliferation and apoptosis were also detected, respectively. Results: Smurf1 was highly expressed in thyroid tumor tissues and thyroid cancer cells. Up-regulation of Smurf1 promoted the viability, migration, invasion and proliferation of thyroid cancer cells. Knockdown of Smurf1 had opposite effects. Moreover, smurf1 promoted the ubiquitination of KISS-1. Overexpression of KISS-1 inactivated NF-κB pathway, suppressed thyroid cancer cell viability, migration, invasion and proliferation, and induced cell apoptosis. Conclusion: Up-regulation of Smurf1 exerted important roles in thyroid cancer formation and development by promoting thyroid cancer proliferation and metastasis. The ubiquitin-dependent degradation of KISS-1 induced by Smurf1 and the activation of NF-κB signaling pathway might be involved in this process. Smurf1 could be an effective therapy target and biomarker for thyroid cancer treatment. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 1015-8987 1421-9778 |
Relation: | https://www.karger.com/Article/FullText/493715; https://doaj.org/toc/1015-8987; https://doaj.org/toc/1421-9778 |
DOI: | 10.1159/000493715 |
URL الوصول: | https://doaj.org/article/63b078e13fec430390522b4a17f94cc6 |
رقم الانضمام: | edsdoj.63b078e13fec430390522b4a17f94cc6 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 10158987 14219778 |
---|---|
DOI: | 10.1159/000493715 |