题名 | SDC4 Gene Silencing Favors Human Papillary Thyroid Carcinoma Cell Apoptosis and Inhibits Epithelial Mesenchymal Transition via Wnt/beta-Catenin Pathway |
作者 | |
发表日期 | 2018-09 |
发表期刊 | MOLECULES AND CELLS 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | epithelial mesenchymal transition Papillary thyroid carcinoma SDC4 Wnt/beta-catenin signaling pathway Epithelial mesenchymal transition Wnt/β-catenin signaling pathway |
其他关键词 | BREAST-CANCER ; CADHERIN ; SYNDECAN-4 ; GROWTH ; ASSOCIATION ; METASTASIS ; MANAGEMENT ; MIGRATION ; MUTATION |
摘要 | As the most common type of endocrine malignancy, papillary thyroid cancer (P1 0 accounts for 85-90% of all thyroid cancers. In this study, we presented the hypothesis that SDC4 gene silencing could effectively attenuate epithelial mesenchymal transition (EMT), and promote cell apoptosis via the Wnt/beta-catenin signaling pathway in human Pit cells. Bioinformatics methods were employed to screen the determined differential expression levels of SDC4 in PTC and adjacent normal samples. PTC tissues and adjacent normal tissues were prepared and their respective levels of SDC4 protein positive expression, in addition to the mRNA and protein levels of SDC4, Wnt/beta-catenin signaling pathway, EMT and apoptosis related genes were all detected accordingly. Flow cytometry was applied in order to detect cell cycle entry and apoptosis. Finaily, analyses of PTC migration and invasion abilities were assessed by using a Transwell assay and scratch test. In PTC tissues, activated Wnt/beta-catenin signaling pathway, increased EMT and repressed cell apoptosis were determined. Moreover, the PTC K1 and TPC-1 cell lines exhibiting the highest SDC4 expression were selected for further experiments. In vitro experiments revealed that SDC4 gene silencing could suppress cell migration, invasion and EMT, while acting to promote the apoptosis of PTC cells by inhibiting the activation of the Wnt/beta-catenin signaling pathway. Besides, si-beta-catenin was observed to inhibit the promotion of PTC cell migration and invasion caused by SDC4 overexpression. Our study revealed that SDC4 gene silencing represses EMT, and enhances cell apoptosis by suppressing the activation of the Wnt/beta-catenin signaling pathway in human PTC. |
资助项目 | Health Department of Zhejiang Province [2018KY510] |
出版者 | KOREAN SOC MOLECULAR & CELLULAR BIOLOGY |
出版地 | SEOUL |
ISSN | 1016-8478 |
EISSN | 0219-1032 |
卷号 | 41期号:9页码:853-867 |
DOI | 10.14348/molcells.2018.0103 |
页数 | 15 |
WOS类目 | Biochemistry & Molecular Biology ; Cell Biology |
WOS研究方向 | Biochemistry & Molecular Biology ; Cell Biology |
WOS记录号 | WOS:000448310000005 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 30165731 |
PMC记录号 | PMC6182223 |
SCOPUSEID | 2-s2.0-85054750809 |
通讯作者地址 | [Wu, Wen-Jun]Department of Endocrinology,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325015,China |
Scopus学科分类 | Molecular Biology;Cell Biology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/15693 |
专题 | 护理学院 附属第一医院_内分泌科 |
通讯作者 | Wu, Wen-Jun |
作者单位 | 1.Department of Surgical Oncology,Ningbo No.2 Hospital,Ningbo,315010,China; 2.School of Nursing,Wenzhou Medical University,Wenzhou,325000,China; 3.Department of Endocrinology,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325015,China |
通讯作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
推荐引用方式 GB/T 7714 | Chen, Liang-Liang,Gao, Ge-Xin,Shen, Fei-Xia,et al. SDC4 Gene Silencing Favors Human Papillary Thyroid Carcinoma Cell Apoptosis and Inhibits Epithelial Mesenchymal Transition via Wnt/beta-Catenin Pathway[J]. MOLECULES AND CELLS,2018,41(9):853-867. |
APA | Chen, Liang-Liang, Gao, Ge-Xin, Shen, Fei-Xia, Chen, Xiong, Gong, Xiao-Hua, & Wu, Wen-Jun. (2018). SDC4 Gene Silencing Favors Human Papillary Thyroid Carcinoma Cell Apoptosis and Inhibits Epithelial Mesenchymal Transition via Wnt/beta-Catenin Pathway. MOLECULES AND CELLS, 41(9), 853-867. |
MLA | Chen, Liang-Liang,et al."SDC4 Gene Silencing Favors Human Papillary Thyroid Carcinoma Cell Apoptosis and Inhibits Epithelial Mesenchymal Transition via Wnt/beta-Catenin Pathway".MOLECULES AND CELLS 41.9(2018):853-867. |
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