Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10758425 | Biochemical and Biophysical Research Communications | 2013 | 7 Pages |
Abstract
miR-21 is overexpressed in tumors and it displays oncogenic activity. Here, we show that expression of miR-21 in primary tumors anticorrelates with KRIT1/CCM1, an interacting partner of the Ras-like GTPase Rap1, involved in Cerebral Cavernous Malformations (CCM). We present evidences that miR-21 silences KRIT1 by targeting its mRNA 3â²UTR and that this interaction is involved in tumor growth control. In fact, miR-21 over-expression or KRIT1 knock-down promote anchorage independent tumor cell growth compared to controls, whereas the opposite is observed when anti-miR-21 or KRIT1 overexpression are employed. Our findings suggest that miR-21 promotes tumor cell growth, at least in part, by down-modulating the potential tumor suppressor KRIT1.
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Authors
Francesca Orso, Fiorella Balzac, Marco Marino, Antonio Lembo, Saverio Francesco Retta, Daniela Taverna,