Upregulation of circ-UBAP2 predicts poor prognosis and promotes triple-negative breast cancer progression through the miR-661/MTA1 pathway

被引:91
作者
Wang, Shengting [1 ]
Li, Qian [1 ]
Wang, Yufang [1 ]
Li, Xiaoming [1 ]
Wang, Rui [1 ]
Kang, Yuhua [1 ]
Xue, Xukai [2 ]
Meng, Rui [1 ]
Wei, Qi [1 ]
Feng, Xinghua [1 ]
机构
[1] Peihua Univ, Dept Clin Med, Xian 710125, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Honghui Hosp, Dept Spine Surg, Xian 710054, Shaanxi, Peoples R China
关键词
circRNA; circ-UBAP2; TNBC; Progression; Prognosis; CIRCULAR RNAS; MICRORNA-661; EXPRESSION; MARKER; MTA1;
D O I
10.1016/j.bbrc.2018.10.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, a large number of studies have shown that circular RNA (circRNA) is involved in the development and progression of human cancer. However, its role in triple-negative breast cancer (TNBC) remains largely unknown. In this study, a novel circRNA, circ-UBAP2 (hsa_circ_0001846), was shown to be markedly upregulated in TNBC. Moreover, high circ-UBAP2 expression was closely associated with larger tumour size (p = 0.003), advanced TNM stage (p = 0.005), lymph node metastasis (p = 0.002), and unfavourable prognosis (p = 0.0256). Functionally, lentivirus-mediated stable knockdown of circ-UBAP2 dramatically weakened the ability of TNBC cells to proliferate and migrate and induced apoptosis in vitro and in vivo. Regarding the mechanism, we found that circ-UBAP2 was mainly observed in the cytoplasm and was capable of sponging miRNA-661 to increase the expression of the oncogene MTA1. Additionally, silencing of miRNA-661 or overexpression of MTA1 could partially rescue the attenuated malignant phenotype caused by circ-UBAP2 knockdown. Taken together, our data reveal that circ-UBAP2 plays a vital regulatory role in TNBC via the miR-661/MTA1 axis and may serve as a promising therapeutic target for TNBC patients. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:996 / 1002
页数:7
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