RETRACTED: The molecular mechanism of microRNA-145 to suppress invasion-metastasis cascade in gastric cancer (Retracted Article)

被引:143
作者
Gao, P. [1 ]
Xing, A-Y [1 ]
Zhou, G-Y [1 ]
Zhang, T-G [1 ]
Zhang, J-P [1 ]
Gao, C. [1 ]
Li, H. [2 ]
Shi, D-B [2 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Pathol, Jinan Wen Hua Xi Rd 107, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Sch Med, Dept Pathol, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
gastric carcinoma; miR-145; metastasis; N-cadherin; N-CADHERIN; TUMOR INVASION; CELL INVASION; EXPRESSION; GROWTH; METALLOPROTEINASES; SIGNATURES; TARGETS;
D O I
10.1038/onc.2012.61
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Invasion and metastasis are the major features of malignant tumors that are responsible for 90% of cancer-related deaths. Recently, microRNAs have been discovered to have a role in suppressing tumor metastasis. This study's aim was to clarify the roles of miR-145 in gastric carcinomas and its underlying molecular mechanism in regulating tumor metastasis. Here, we demonstrate a stepwise downregulation of miR-145 level in nontumorous gastric mucosa, primary gastric cancers-and their secondary metastases. In vitro analysis of miR-145's ectopic expression and loss-of-function suggests that it suppresses gastric cancer cell migration and invasion. In vivo spontaneous metastasis and experimental metastasis assay further confirm its function in suppressing the invasion-metastasis cascade, including impairing local invasion and inhibiting hematogenous metastasis in gastric cancers. Furthermore, we identified a novel mechanism of miR-145 to suppress metastasis. N-cadherin (CDH2) was proved to be a direct target of miR-145, using luciferase assay and western blot. Re-expressing N-cadherin in miR-145-transfected cells reverses their migration and invasion defects. Although not a direct target of miR-145, matrix metallopeptidase 9 (MMP9), but not MMP2, was also significantly decreased in miR-145-expressing cells. We suggest that miR-145 suppresses tumor metastasis by inhibiting N-cadherin protein translation, and then indirectly downregulates its downstream effector MMP9. Oncogene (2013) 32, 491-501; doi:10.1038/onc.2012.61; published online 27 February 2012
引用
收藏
页码:491 / 501
页数:11
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