MiR-26a inhibits thyroid cancer cell proliferation by targeting ARPP19

被引:4
作者
Gong, Yanping [1 ]
Wu, Wenshuang [1 ]
Zou, Xiuhe [1 ]
Liu, Feng [1 ]
Wei, Tao [1 ]
Zhu, Jingqiang [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Thyroid & Parathyroid Surg Ctr, Chengdu 610041, Sichuan, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2018年 / 8卷 / 06期
关键词
ARPP19; cell proliferation; miR-26a; tamoxifen; thyroid cancer; IN-VITRO; EXPRESSION; CARCINOMAS; MICRORNA; GROWTH; APOPTOSIS; MIGRATION; THERAPY; ARPP-19; REGIONS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
miRNA, which involves in pathogenesis of thyroid cancer via different targets, has been found aberrantly expressed in thyroid cancer. Modes of actions of miR-26a in papillary thyroid carcinoma (PTC), however, have not been fully understood to this date. In vitro results obtained from this research confirmed miR-26a was down-regulated in PTC cells (i.e. TPC-1 and BCPAP) where the down-regulation of miR-26a was found to be able to promote cell proliferation. In order to explore the mechanisms, potential targets of miR-26a were postulated: cAMP regulated phosphoprotein 19 (ARPP19) turned out to be the target of miR-26a and it was by depleting ARPP19 was the cell proliferation be suppressed. This suggested that miR-26a regulated cell proliferation by targeting ARPP19. In addition, such a depletion of ARPP19 sensitized PTC cells to tamoxifen (TMX) treatment. The above findings indicated miR-26a was a target of interest regarding the treatment of refractory thyroid carcinomas.
引用
收藏
页码:1030 / 1039
页数:10
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