Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/125584
Title: miR-1269 promotes metastasis and forms a positive feedback loop with TGF-β
Author: Bu, Pengcheng
Wang, Lihua
Chen, Kai-Yuan
Rakhilin, Nikolai
Sun, Jian
Closa, Adrià
Tung, Kuei-Ling
King, Sarah
Kristine Varanko, Anastasia
Xu, Yitian
Huan Chen, Joyce
Zessin, Amelia S.
Shealy, James
Cummings, Bethany
Hsu, David
Lipkin, Steven M.
Moreno Aguado, Víctor
Gümüş, Zeynep H.
Shen, Xiling
Keywords: Càncer
Quimioteràpia del càncer
Metàstasi
Cancer
Cancer chemotherapy
Metastasis
Issue Date: 15-Apr-2015
Publisher: Nature Publishing Group
Abstract: 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.
Note: Reproducció del document publicat a: https://doi.org/10.1038/ncomms7879.
It is part of: Nature Communications, 2015, vol. 15, num. 6, p. 6879
URI: http://hdl.handle.net/2445/125584
Related resource: https://doi.org/10.1038/ncomms7879.
ISSN: 2041-1723
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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