The microRNAs miR-373 and miR-520c promote tumour invasion and metastasis
MicroRNAs (miRNAs) are single-stranded, noncoding RNAs that are important in many biological processes1, 2. Although the oncogenic and tumour-suppressive functions of several miRNAs have been characterized, the role of miRNAs in mediating tumour metastasis was addressed only recently3 and still remains largely unexplored4, 5. To identify potential metastasis-promoting miRNAs, we set up a genetic screen using a non-metastatic, human breast tumour cell line that was transduced with a miRNA-expression library and subjected to a trans-well migration assay. We found that human miR-373 and miR-520c stimulated cancer cell migration and invasion in vitro and in vivo, and that certain cancer cell lines depend on endogenous miR-373 activity to migrate efficiently. Mechanistically, the migration phenotype of miR-373 and miR-520c can be explained by suppression of CD44. We found significant upregulation of miR-373 in clinical breast cancer metastasis samples that correlated inversely with CD44 expression. Taken together, our findings indicate that miRNAs are involved in tumour migration and invasion, and implicate miR-373 and miR-520c as metastasis-promoting miRNAs.
http://www.nature.com/ncb/journal/v10/n2/abs/ncb1681.html
Monday, February 4, 2008
microRNAs
Posted by Chart Smart at 3:15 PM
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment