MicroRNA-375 suppresses human colorectal cancer metastasis by targeting Frizzled 8

被引:50
|
作者
Xu, Lingling [1 ]
Wen, Tao [2 ]
Liu, Zhe [1 ]
Xu, Feng [1 ]
Yang, Lei [2 ]
Liu, Jian [2 ]
Feng, Guosheng [1 ]
An, Guangyu [1 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Dept Oncol, Beijing 100020, Peoples R China
[2] Capital Med Univ, Beijing Chao Yang Hosp, Med Res Ctr, Beijing 100020, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; microRNA-375; metastasis; FZD8; TO-MESENCHYMAL TRANSITION; TUMOR-SUPPRESSOR; BONE METASTASIS; HUMAN COLON; INVASION; EXPRESSION; CARCINOMA; GROWTH; CONTRIBUTES; PROGRESSION;
D O I
10.18632/oncotarget.9811
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
microRNAs are aberrantly expressed during the development and progression of a variety of human cancers, including colorectal cancer (CRC). Of these microRNAs, microRNA-375 (miR-375) was previously observed to be downregulated in human colorectal cancer(CRC) plasma and tissues, but its functions are largely unknown. Here, we investigated the impact of miR-375 on CRC metastasis. Specifically, miR-375 expression was significantly decreased in human CRC tissues compared with their matched noncancerous tissues (NCTs), and low levels of miR-375 predicted tumor metastatic potential. The up-regulation of miR-375 suppressed colorectal cancer cell migration and invasion in vitro and reduced tumor metastases in murine models established by both orthotopic implantation and spleen injection. Furthermore, we identified Frizzled 8 (FZD8) as a direct target of miR-375 in CRC, and miR-375 negatively regulated Wnt/beta-catenin signaling by suppressing FZD8. More importantly, FZD8 expression inversely correlated with overall survival in human CRC patients and is a likely independent predictor of survival. Therefore, we concluded that miR-375 functions as a tumor-suppressive microRNA by directly acting upon FZD8, which may serve as a new therapeutic target to inhibit tumor metastasis in CRC.
引用
收藏
页码:40644 / 40656
页数:13
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