| Title | miR-1269 promotes metastasis and forms a positive feedback loop with TGF-β. | 
| Publication Type | Journal Article | 
| Year of Publication | 2015 | 
| Authors | Bu, P, Wang, L, Chen, K-Y, Rakhilin, N, Sun, J, Closa, A, Tung, K-L, King, S, Varanko, AKristine, Xu, Y, Chen, JHuan, Zessin, AS, Shealy, J, Cummings, B, Hsu, D, Lipkin, SM, Moreno, V, Gümüş, ZH, Shen, X | 
| Journal | Nat Commun | 
| Volume | 6 | 
| Pagination | 6879 | 
| Date Published | 2015 | 
| ISSN | 2041-1723 | 
| Abstract | <p>As patient survival drops precipitously from early-stage cancers to late-stage and metastatic cancers, microRNAs that promote relapse and metastasis can serve as prognostic and predictive markers as well as therapeutic targets for chemoprevention. Here we show that miR-1269a promotes colorectal cancer (CRC) metastasis and forms a positive feedback loop with TGF-β signalling. miR-1269a is upregulated in late-stage CRCs, and long-term monitoring of 100 stage II CRC patients revealed that miR-1269a expression in their surgically removed primary tumours is strongly associated with risk of CRC relapse and metastasis. Consistent with clinical observations, miR-1269a significantly increases the ability of CRC cells to invade and metastasize in vivo. TGF-β activates miR-1269 via Sox4, while miR-1269a enhances TGF-β signalling by targeting Smad7 and HOXD10, hence forming a positive feedback loop. Our findings suggest that miR-1269a is a potential marker to inform adjuvant chemotherapy decisions for CRC patients and a potential therapeutic target to deter metastasis.</p> | 
| DOI | 10.1038/ncomms7879 | 
| Alternate Journal | Nat Commun | 
| PubMed ID | 25872451 | 
| PubMed Central ID | PMC4399006 | 
| Grant List | R01 GM095990 / GM / NIGMS NIH HHS / United States R01GM95990 / GM / NIGMS NIH HHS / United States | 
 
        