MiR-93 Inhibits Trophoblast Cell Proliferation and Promotes Cell Apoptosis by Targeting BCL2L2 in Recurrent Spontaneous Abortion

被引:0
作者
Hai-Ning Liu
Xiu-Ming Tang
Xue-Qin Wang
Jing Gao
Ni Li
Yong-Yong Wang
Hong-Fei Xia
机构
[1] Shandong University,Center for Reproductive Medicine
[2] Qingdao Municipal Hospital,Department of Reproductive Medicine
[3] Qingdao University,Reproductive and Genetic Center
[4] National Research Center for Assisted Reproductive Technology and Reproductive Genetics,Graduate School
[5] National Research Institute for Family Planning,Department of Reproductive Medicine
[6] Peking Union Medical College,undefined
[7] The Affiliated Hospital of Qingdao University,undefined
来源
Reproductive Sciences | 2020年 / 27卷
关键词
Recurrent spontaneous abortion; Trophoblast cells;
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学科分类号
摘要
Recurrent spontaneous abortion (RSA) is a common health problem that affects 1–5% of women in reproductive age. Plenty of studies have indicated that microRNAs (miRNAs) are involved in the occurrence of miscarriage. MiR-93 has a wide range of functions in mammalian tissues and plays an important role in many diseases especially for cancers. However, it remains unknown whether miR-93 is associated with human RSA. In this report, clinical samples revealed that miR-93 expression was significantly elevated in the villi tissues of RSA patients. Upregulation of miR-93 inhibited human trophoblast cells HTR-8/SVneo cell proliferation, migration, and invasiveness, but promoted cell apoptosis in vitro. Conversely, the downregulation of miR-93 reversed these effects. Bcl-2 like protein 2 (BCL2L2), a potential target gene of miR-93, was inversely correlated with miR-93 expression in the villi of clinical samples. Furthermore, the luciferase reporter system demonstrated that miR-93 directly downregulated the expression of BCL2L2 by binding a specific sequence of its 3′-untranslated region (3′UTR). Collectively, these data strongly suggest that miR-93 regulates trophoblast cell proliferation, migration, invasive, and apoptosis by targeting BCL2L2 expression and is involved in the pathogenesis of RSA.
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页码:152 / 162
页数:10
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