Breast Cancer Online (2008), 11:e2 Cambridge University Press
Copyright © Cambridge University Press 2008
doi:10.1017/S1470903108006688
Alex Swarbricka1 c1
a1 Cancer Research Program, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia
Abstract
Citation of the original article: L. Ma, J. Teruya-Feldstein, R. A. Weinberg. Nature 2007; 449(7163): 682–688; Epub 26 September 2007.
Abstract of the original article: MicroRNAs have been implicated in regulating diverse cellular pathways. Although there is emerging evidence that some microRNAs can function as oncogenes or tumour suppressors, the role of microRNAs in mediating cancer metastasis remains unexplored. Here we show, using a combination of mouse and human cells, that microRNA-10b (miR-10b) is highly expressed in metastatic breast cancer cells and positively regulates cell migration and invasion. Overexpression of miR-10b in otherwise non-metastatic breast tumours initiates robust invasion and metastasis. Expression of miR-10b is induced by the transcription factor Twist, which binds directly to the putative promoter of miR-10b (MIRN10B). The miR-10b induced by Twist proceeds to inhibit translation of the messenger RNA encoding homeobox D10, resulting in increased expression of a well-characterized pro-metastatic gene, RhoC. Significantly, the level of miR-10b expression in primary breast carcinomas correlates with clinical progression. These findings suggest the workings of an undescribed regulatory pathway, in which a pleiotropic transcription factor induces expression of a specific microRNA, which suppresses its direct target and in turn activates another pro-metastatic gene, leading to tumour cell invasion and metastasis.
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