LncRNA AWPPH and miRNA-21 regulates cancer cell proliferation and chemosensitivity in triple-negative breast cancer by interacting with each other

被引:54
作者
Liu, Ai-Na [1 ]
Qu, Hua-Jun [1 ]
Gong, Wen-Jing [1 ]
Xiang, Jin-Yu [1 ]
Yang, Miao-Miao [1 ]
Zhang, Wei [2 ]
机构
[1] Qingdao Univ Med Coll, Yantai Yuhuangding Hosp, Dept Oncol, Yantai, Shandong, Peoples R China
[2] Qingdao Univ Med Coll, Affiliated Yantai Yuhuangding Hosp, Dept Radiotherapy, 20 East Yuhuangding Rd, Yantai 264000, Shandong, Peoples R China
关键词
cell proliferation; chemosensitivity; long-non-coding RNA AWPPH; microRNA-21; triple-negative breast cancer; LONG NONCODING RNA; MIR-21; MICRORNA-21; GAS5;
D O I
10.1002/jcb.28747
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
Long-non-coding RNAs (lncRNA) AWPPH promotes the progression of liver and bladder cancer, indicating its oncogenic role. The current study aimed to explore the involvement of AWPPH in triple-negative breast cancer (TNBC). In the current study, we found that plasma levels of lncRNA AWPPH and microRNA-21 (miRNA-21) were upregulated in patients with TNBC than in healthy controls, and the upregulation of plasma lncRNA AWPPH and miRNA-21 distinguished early-stage patients with TNBC from healthy controls. Plasma levels of lncRNA AWPPH and miRNA-21 were significantly and positively correlated in both patients with TNBC and healthy controls. LncRNA AWPPH and miRNA-21 overexpression led to promoted cancer cells proliferation and improved cancer cell viability under carboplatin treatment, while lncRNA AWPPH small interfering RNA (siRNA) silencing played an opposite role. In addition, miRNA-21 overexpression attenuated the effects of lncRNA AWPPH siRNA silencing on of cancer cell behaviors. LncRNA AWPPH overexpression led to upregulated miRNA-21 in TNBC cells, while miRNA-21 overexpression also led to significantly upregulated lncRNA AWPPH expression. Therefore, lncRNA AWPPH and miRNA-21 may regulate cancer cell proliferation and chemosensitivity in TNBC by interacting with each other.
引用
收藏
页码:14860 / 14866
页数:7
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