MicroRNA-488 inhibits proliferation and motility of tumor cells via downregulating FSCN1, modulated by Notch3 in breast carcinomas

被引:20
作者
Wu, Yang [1 ]
Yuan, Ming-Heng [1 ]
Wu, Hua-Tao [2 ]
Chen, Wen-Jia [1 ,3 ]
Zhang, Man-Li [1 ]
Ye, Qian-Qian [1 ,3 ]
Liu, Jing [1 ,3 ]
Zhang, Guo-Jun [1 ,4 ]
机构
[1] Shantou Univ, Changjiang Scholars Lab, Guangdong Prov Key Lab Diag & Treatment Breast Ca, Med Coll, Shantou 515041, Peoples R China
[2] Shantou Univ, Dept Gen Surg, Affiliated Hosp 1, Med Coll, Shantou 515041, Peoples R China
[3] Shantou Univ, Dept Physiol, Canc Res Ctr, Med Coll, Shantou 515041, Peoples R China
[4] Xiamen Univ, Dept Breast & Thyroid, Xiangan Hosp, Xiamen 361101, Peoples R China
基金
中国国家自然科学基金;
关键词
CANCER; PROMOTES; METASTASIS; INVASION;
D O I
10.1038/s41419-020-03121-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As important modulators in multiple physiological processes, microRNAs (miRNAs) have been reported in various malignant tumors, including breast cancer. The current study investigated the function of a new tumor suppressor microRNA, miR-488, and its molecular mechanism of metastasis in breast cancers. CCK8 and transwell assays revealed that the upregulated miR-488 level significantly inhibited the proliferation and migration of breast cancer cells. As a potential downstream gene, the mRNA and protein level of FSCN1 was suppressed by increased miR-488 and vice versa. Luciferase assay showed that miR-488 directly bind to the 3 ' UTR of FSCN1 and suppressed the translation process of FSCN1. The promoter region of miR-488 was directly bound by Notch3 and promoted the expression of miR-488 transcriptionally. Immunohistochemistry results revealed that in patients with breast cancer, the expression of Notch3 and were negatively correlated with the FSCN1 levels significantly. Therefore, the current finding predicted miR-488 as a tumor suppressor molecule in breast cancer, and demonstrated that Notch3/miR-488/FSCN1 axis is established and involved in regulating the metastasis of breast cancers, providing novel therapeutic targets for patients with breast cancers.
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收藏
页数:13
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