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Long noncoding RNA MALAT1-regulated microRNA 506 modulates ovarian cancer growth by targeting iASPP
被引:60
作者:
Lei, Ruilin
[1
,2
]
Xue, Min
[2
]
Zhang, Lan
[1
]
Lin, ZhongQiu
[1
]
机构:
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Obstet & Gynecol, Guangdong Prov Key Lab Malignant Tumor Epigenet &, 107 Yan Jiang West Rd, Guangzhou 510120, Guangdong, Peoples R China
[2] Cent S Univ, Xiangya Hosp 3, Dept Obstet & Gynecol, Changsha, Hunan, Peoples R China
来源:
ONCOTARGETS AND THERAPY
|
2017年
/
10卷
关键词:
lncRNA;
MALAT1;
miR-506;
ovarian cancer;
iASPP;
CELL-PROLIFERATION;
HUMAN OSTEOSARCOMA;
MALAT1;
PROMOTES;
KIDNEY CANCER;
CARCINOMA;
MIGRATION;
TUMOR;
METASTASIS;
EXPRESSION;
MIR-376A;
D O I:
10.2147/OTT.S112686
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
MALAT1, an important cancer-associated long noncoding RNA (lncRNA), contributes to the development and progression of several cancers. Disordered expression of MALAT1 has been observed in several cancers, including cervical cancer, breast cancer, and ovarian cancer. However, the exact effects and molecular mechanisms of MALAT1 in ovarian cancer progression are still unknown. Here, we investigated the role of MALAT1 in human ovarian cancer cell lines and clinical tumor samples, in order to determine the function of this molecule. In our research, lncRNA-MALAT1 was specifically upregulated in ovarian cancer cell lines and promoted ovarian cancer-cell growth through targeting microRNA (miR)-506. Knockdown of MALAT1 inhibited the proliferation and DNA synthesis of human ovarian cancer cell in vitro. In addition, miR-506-dependent iASPP regulation was required in MALAT1-induced ovarian cancer-cell growth. These findings indicated that MALAT1 might suppress tumor growth via miR-506-dependent iASPP regulation. Taken together, our data indicated that MALAT1 might be an oncogenic lncRNA that promotes proliferation of ovarian cancer and could be regarded as a therapeutic target in human ovarian cancer.
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页码:35 / 46
页数:12
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