miR-1269 promotes metastasis and forms a positive feedback loop with TGF-β

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作者
Pengcheng Bu
Lihua Wang
Kai-Yuan Chen
Nikolai Rakhilin
Jian Sun
Adria Closa
Kuei-Ling Tung
Sarah King
Anastasia Kristine Varanko
Yitian Xu
Joyce Huan Chen
Amelia S. Zessin
James Shealy
Bethany Cummings
David Hsu
Steven M. Lipkin
Victor Moreno
Zeynep H. Gümüş
Xiling Shen
机构
[1] School of Electrical and Computer Engineering,Department of Biomedical Engineering
[2] Cornell University,Department of Biological and Environmental Engineering
[3] Cornell University,Departments of Medicine
[4] Cornell University,Department of Physiology and Biophysics
[5] Genetic Medicine and Surgery,Department of Clinical Sciences
[6] Weill Cornell Medical College,Division of Medical Oncology
[7] Weill Cornell Medical College,Department of Biomedical Sciences
[8] University of Barcelona,Department of Genetics and Genomic Sciences
[9] Cancer Prevention and Control Program,undefined
[10] Catalan Institute of Oncology-IDIBELL,undefined
[11] CIBERESP,undefined
[12] Duke Cancer Institute,undefined
[13] Duke University,undefined
[14] Cornell University,undefined
[15] Icahn School of Medicine at Mount Sinai,undefined
[16] Icahn Institute for Genomics and Multiscale Biology,undefined
[17] Icahn School of Medicine at Mount Sinai,undefined
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摘要
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.
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