Long non-coding RNA DILC suppresses bladder cancer cells progression

生物 膀胱癌 癌症研究 转移 长非编码RNA 肿瘤进展 车站3 抑制器 结直肠癌 癌症 细胞生长 核糖核酸 信号转导 基因 细胞生物学 遗传学
作者
Qian-Yun Ma,Shuying Li,Xi-Zhou Li,Tengfei Zhou,Yongfu Zhao,Fang-Lin Liu,Xiaona Yu,Jian Lin,Fan-Yue Chen,Jie Cao,Huijun Xi,Hengyu Li
出处
期刊:Gene [Elsevier BV]
卷期号:710: 193-201 被引量:10
标识
DOI:10.1016/j.gene.2019.06.009
摘要

Accumulative researches have demonstrated the critical functions of long non-coding RNAs (lncRNAs) in the progression of malignant tumors, including bladder cancer (BC). Our previous studies showed that lnc-DILC was an important tumor suppressor gene in both liver cancer and colorectal cancer. However, the role of lnc-DILC in BC remains to be elucidated. In the present study, we for first found that lnc-DILC was downregulated in human bladder cancer tissues. Lnc-DILC overexpression suppressed the proliferation, metastasis and expansion of bladder cancer stem cells (CSCs). Mechanically, lnc-DILC suppressed BC cells progression via STAT3 pathway. Special STAT3 inhibitor S3I-201 diminished the discrepancy of growth, metastasis and self-renewal ability between lnc-DILC-overexpression BC cells and their control cells, which further confirmed that STAT3 was acquired for lnc-DILC-disrupted BC cell growth, metastasis and self-renewal. Taken together, our results suggest that lnc-DILC is a novel bladder tumor suppressor and indicate that lnc-DILC inhibits BC progression via inactivating STAT3 signaling.

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