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 |