Knockdown of Long Noncoding RNA CAT104 Inhibits the Proliferation, Migration, and Invasion of Human Osteosarcoma Cells by Regulating MicroRNA-381

被引:20
作者
Xia, Bo [1 ]
Wang, Lei [2 ]
Feng, Li [1 ]
Tian, Baofang [1 ]
Tan, Yuanjie [3 ]
Du, Baoyin [1 ]
机构
[1] Jining 1 Peoples Hosp, Dept Emergency Trauma Surg, 6 Jiankang Rd, Jining 272011, Shandong, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Affiliated Hosp 2, Dept Orthoped 2, Jinan, Shandong, Peoples R China
[3] Weihai Hosp Tradit Chinese Med, Dept Cardiol, Weihai, Shandong, Peoples R China
关键词
Osteosarcoma; Long noncoding RNA CAT104; MicroRNA-381; JNK pathway; Zinc-finger E-box-binding homeohox 1 (ZEB1); Wnt/beta-catenin pathway; MESENCHYMAL TRANSITION; DOWN-REGULATION; CANCER CELLS; METASTASIS; MIR-381; EXPRESSION; PROMOTES; PATHOGENESIS; PROGRESSION;
D O I
10.3727/096504018X15199511344806
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is the most common primary malignant bone tumor in children and adolescents. This study aimed to explore the effects of long noncoding RNA CAT104 and microRNA-381 (miR-381) on osteosarcoma cell proliferation, migration, invasion, and apoptosis, as well as the underlying potential mechanism. We found that CAT104 was highly expressed in osteosarcoma MG63 and OS-732 cells. Knockdown of CAT104 significantly inhibited OS-732 cell proliferation, migration, and invasion, but promoted cell apoptosis. CAT104 regulated the expression of miR-381, and miR-381 participated in the effects of CAT104 on OS-732 cells. Zinc finger E-box-binding homeobox 1 (ZEB1) was a direct target gene of miR-381, which was involved in the regulatory roles of miR-381 in OS-732 cell proliferation, migration, invasion, and apoptosis, as well as c-Jun N-terminal kinase (JNK) and Wnt/beta-catenin pathways. In conclusion, our research verified that suppression of CAT104 exerted significant inhibitory effects on osteosarcoma cell proliferation, migration, and invasion by regulating the expression of miR-381 and downstream ZEB1, as well as JNK and Wnt/beta-catenin pathways.
引用
收藏
页码:89 / 98
页数:10
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