Artesunate suppresses the viability and mobility of prostate cancer cells through UCA1, the sponge of miR-184

被引:61
作者
Zhou, Yan [1 ]
Wang, Xiuju [2 ]
Zhang, Jianjun [1 ]
He, Aina [1 ]
Wang, Ya Ling [1 ]
Han, Kun [1 ]
Su, Yang [1 ]
Yin, Junyi [1 ]
Lv, Xiaobin [3 ]
Hu, Haiyan [1 ]
机构
[1] Shanghai Jiao Tong Univ Affiliated Sixth Peoples, Oncol Dept, Shanghai 200233, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Guangdong Higher Educ Inst, Key Lab Malignant Tumor Gene Regulat & Target The, Guangzhou 510282, Guangdong, Peoples R China
[3] Nanchang Univ, Cent Lab Third Affiliated Hosp, Nanchang 330008, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
artesunate; prostate cancer; metastasis; UCA1; miR-184; NONCODING RNA UCA1; TUMOR-GROWTH; PROLIFERATION; RESISTANCE; CARCINOMA; IDENTIFICATION; ARTEMISININ; INHIBITION; MICRORNA; INVASION;
D O I
10.18632/oncotarget.15353
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Artesunate (ART) is a sesquiterpene lactone isolated from the leafy portions of the Chinese herb Artemisia annua. Here, we evaluated the effect of ART on the prostate cancer (PCa) cell lines DU145 and LNCaP and explored its potential mechanisms. ART inhibited the viability and mobility of DU145 and LNCaP cells. Mechanistically, we found that UCA1, one of the most important lncRNAs in malignancies of the urinary system, may be a potential mediator contributing to the tumor suppressor function of ART. First, the UCA1 level was reduced significantly after being exposed to ART. In addition, UCA1 was up-regulated in prostate cancer tissues compared to hyperplastic prostatic tissues, and a higher UCA1 level predicted poor prognosis in PCa patients. Furthermore, reintroduction of UCA1 into PCa cells reversed the effect of ART on apoptosis and metastatic ability. Then we determined that the miR-184/Bcl-2 axis might be the downstream signaling pathway of UCA1 upon ART treatment. UCA1 binds to miR-184 through its seed sequences and may function as a sponge for miR-184.
引用
收藏
页码:18260 / 18270
页数:11
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