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Integrated analysis identifies DUSP5 as a novel prognostic indicator for thyroid follicular carcinoma.

Authors :
Zhang, Qian
Xing, Yiqian
Jiang, Shan
Xu, Chunmei
Zhou, Xiaojun
Zhang, Rui
Xie, Tianyue
Zou, Zhiwei
Gong, Piyun
Zhu, Huangao
Zhang, Dongmei
Ma, Huimei
Liao, Lin
Dong, Jianjun
Source :
Thoracic Cancer; Feb2020, Vol. 11 Issue 2, p336-345, 10p
Publication Year :
2020

Abstract

Background: Differentiated thyroid cancer involves thyroid follicular carcinoma (FTC) and papillary thyroid carcinoma (PTC). Patients with FTC have a worse prognosis than those with PTC for early metastasis through blood of FTC. However, the mechanism of poor prognosis of FTC is still unclear. Here, we aim to evaluate the role of DUSP5 in the prognostic evaluation of FTC. Method: We searched the Gene Expression Omnibus (GEO) database for the differentially expressed genes (DEGs) between FTC and PTC, and then combined with survival analysis of cBioPortal database to locate the gene significantly related to prognosis. Tissue microarrays and clinical tissues were used to examine DUSP5 expression by immunohistochemical (IHC) staining between FTC and PTC tissues. In vitro experiment, proliferation, migration and invasion of FTC were observed after regulation of DUSP5 by transfection of siRNA and plasmids, respectively. Results: After searching the GEO database, 26 DEGs were found. DUSP5 was significantly associated with prognosis of FTC in combination with survival analysis. Data of IHC staining showed lower expression of DUSP5 in FTC compared to PTC tissues. Furthermore, overexpression of DUSP5 inhibited the proliferation, migration and invasion accompanied with low level of MMP9 and Vimentin and high level of E‐cadherin. Nevertheless, inhibition of DUSP5 ameliorated above damaging effect on the proliferation, migration and invasion. Conclusion: DUSP5 was differentially expressed in FTC and PTC tissues. Low level of DUSP5 in FTC participates in the high frequency of metastasis, and further contributes to poor prognosis of FTC. DUSP5 could be served as a novel therapeutic target for FTC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17597706
Volume :
11
Issue :
2
Database :
Complementary Index
Journal :
Thoracic Cancer
Publication Type :
Academic Journal
Accession number :
141526879
Full Text :
https://doi.org/10.1111/1759-7714.13270