- Bu, Pengcheng;
- Wang, Lihua;
- Chen, Kai-Yuan;
- Rakhilin, Nikolai;
- Sun, Jian;
- Closa, Adria;
- Tung, Kuei-Ling;
- King, Sarah;
- Kristine Varanko, Anastasia;
- Xu, Yitian;
- Huan Chen, Joyce;
- Zessin, Amelia;
- Shealy, James;
- Hsu, David;
- Lipkin, Steven;
- Moreno, Victor;
- Gümüş, Zeynep;
- Shen, Xiling;
- Cummings, Bethany
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.