Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1

Background. Thyroid carcinoma (TC) is one of the frequent endocrine malignancies, and growing evidence suggests that aberrant microRNA (miRNA) expression contributes to TC development and progression. Nevertheless, the function of miR-330-5p in the progression of TC remains unknown. Methods. The exp...

Full description

Bibliographic Details
Main Authors: Yuxia Wang, Zhaozhe Liu, Xiangning Ren, Nan Sun, Qiuhua Li, Che Bian
Format: Article
Language:English
Published: Hindawi Limited 2021-01-01
Series:Journal of Oncology
Online Access:http://dx.doi.org/10.1155/2021/1070365
id doaj-38daff5323874687ad0ede8dab24a5b2
record_format Article
spelling doaj-38daff5323874687ad0ede8dab24a5b22021-07-12T02:12:31ZengHindawi LimitedJournal of Oncology1687-84692021-01-01202110.1155/2021/1070365Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1Yuxia Wang0Zhaozhe Liu1Xiangning Ren2Nan Sun3Qiuhua Li4Che Bian5Department of EndocrinologyOncology DepartmentDepartment of EndocrinologyDepartment of EndocrinologyOncology DepartmentDepartment of EndocrinologyBackground. Thyroid carcinoma (TC) is one of the frequent endocrine malignancies, and growing evidence suggests that aberrant microRNA (miRNA) expression contributes to TC development and progression. Nevertheless, the function of miR-330-5p in the progression of TC remains unknown. Methods. The expression levels of miR-330-5 in patients with thyroid carcinoma and healthy controls were detected, and their potential diagnostic and prognostic values were analyzed. Results. In this study, we firstly found that miR-330-5p expression was markedly upregulated in TC tissue and cell lines. Functionally, the downregulation of miR-330-5p suppressed TC cell proliferation, migration, and invasion. Further studies revealed that miR-330-5p negatively regulated the expression of forkhead box E1 (FOXE1). More importantly, the results of rescue experiments suggested that FOXE1 overexpression reduced the positive effects of miR-330-5p overexpression in TPC-1 and K-1 cells. Conclusions. This work revealed that miR-330-5p facilitated the TC progression through targeting FOXE1, which may offer novel therapeutic options for TC.http://dx.doi.org/10.1155/2021/1070365
collection DOAJ
language English
format Article
sources DOAJ
author Yuxia Wang
Zhaozhe Liu
Xiangning Ren
Nan Sun
Qiuhua Li
Che Bian
spellingShingle Yuxia Wang
Zhaozhe Liu
Xiangning Ren
Nan Sun
Qiuhua Li
Che Bian
Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
Journal of Oncology
author_facet Yuxia Wang
Zhaozhe Liu
Xiangning Ren
Nan Sun
Qiuhua Li
Che Bian
author_sort Yuxia Wang
title Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
title_short Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
title_full Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
title_fullStr Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
title_full_unstemmed Hsa-miR-330-5p Aggravates Thyroid Carcinoma via Targeting FOXE1
title_sort hsa-mir-330-5p aggravates thyroid carcinoma via targeting foxe1
publisher Hindawi Limited
series Journal of Oncology
issn 1687-8469
publishDate 2021-01-01
description Background. Thyroid carcinoma (TC) is one of the frequent endocrine malignancies, and growing evidence suggests that aberrant microRNA (miRNA) expression contributes to TC development and progression. Nevertheless, the function of miR-330-5p in the progression of TC remains unknown. Methods. The expression levels of miR-330-5 in patients with thyroid carcinoma and healthy controls were detected, and their potential diagnostic and prognostic values were analyzed. Results. In this study, we firstly found that miR-330-5p expression was markedly upregulated in TC tissue and cell lines. Functionally, the downregulation of miR-330-5p suppressed TC cell proliferation, migration, and invasion. Further studies revealed that miR-330-5p negatively regulated the expression of forkhead box E1 (FOXE1). More importantly, the results of rescue experiments suggested that FOXE1 overexpression reduced the positive effects of miR-330-5p overexpression in TPC-1 and K-1 cells. Conclusions. This work revealed that miR-330-5p facilitated the TC progression through targeting FOXE1, which may offer novel therapeutic options for TC.
url http://dx.doi.org/10.1155/2021/1070365
work_keys_str_mv AT yuxiawang hsamir3305paggravatesthyroidcarcinomaviatargetingfoxe1
AT zhaozheliu hsamir3305paggravatesthyroidcarcinomaviatargetingfoxe1
AT xiangningren hsamir3305paggravatesthyroidcarcinomaviatargetingfoxe1
AT nansun hsamir3305paggravatesthyroidcarcinomaviatargetingfoxe1
AT qiuhuali hsamir3305paggravatesthyroidcarcinomaviatargetingfoxe1
AT chebian hsamir3305paggravatesthyroidcarcinomaviatargetingfoxe1
_version_ 1721307993099730944