Myc/miR-378/TOB2/cyclin D1 functional module regulates oncogenic transformation

被引:72
作者
Feng, M. [1 ]
Li, Z. [1 ]
Aau, M. [1 ]
Wong, C. H. [1 ]
Yang, X. [1 ]
Yu, Q. [1 ,2 ,3 ]
机构
[1] ASTAR, Dept Canc Biol & Pharmacol, Genome Inst Singapore, Biopolis 138672, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore 117595, Singapore
[3] DUKE NUS Med Sch, Dept Canc & Stem Cell Biol, Singapore, Singapore
关键词
Myc; miR-378; TOB2; cyclin D1; C-MYC; MESENCHYMAL TRANSITION; CELL-PROLIFERATION; CANCER METASTASIS; MIR-200; FAMILY; E-CADHERIN; MICRORNA; TARGET; RAS; APOPTOSIS;
D O I
10.1038/onc.2010.602
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
The c-Myc transcription factor activates a cascade of downstream targets to form a complex transcriptional program that ultimately leads to cellular transformation. Although a large number of protein-encoding genes as well as non-coding RNAs were identified as Myc targets, only a few have been validated to be functionally important for c-Myc-driven transformation. Here, we identify a microRNA (miRNA), miR-378, as a novel target of the c-Myc oncoprotein that is able to cooperate with activated Ras or HER2 to promote cellular transformation. Mechanistically, miR-378 achieves this oncogenic effect, at least in part, by targeting and inhibiting the anti-proliferative BTG family member, TOB2, which is further elucidated as a candidate tumor suppressor to transcriptionally repress proto-oncogene cyclin D1. Therefore, our study identifies miR-378-TOB2-cyclin D1 as a functional module to mediate the cross talk between Myc and Ras signaling in cellular transformation. Oncogene (2011) 30, 2242-2251; doi:10.1038/onc.2010.602; published online 17 January 2011
引用
收藏
页码:2242 / 2251
页数:10
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