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Less is more: low expression of MT1-MMP is optimal to promote migration and tumourigenesis of breast cancer cells.
Mol Cancer. 2016 Oct 18;15(1):65. doi: 10.1186/s12943-016-0547-x.
Mol Cancer. 2016.
PMID: 27756325
Free PMC article.
The cytoplasmic domain of MT1-MMP is dispensable for migration augmentation but necessary to mediate viability of MCF-7 breast cancer cells.
Cepeda MA, Pelling JJ, Evered CL, Leong HS, Damjanovski S.
Cepeda MA, et al. Among authors: evered cl.
Exp Cell Res. 2017 Jan 1;350(1):169-183. doi: 10.1016/j.yexcr.2016.11.019. Epub 2016 Nov 23.
Exp Cell Res. 2017.
PMID: 27889376
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Inhibition of MT1-MMP proteolytic function and ERK1/2 signalling influences cell migration and invasion through changes in MMP-2 and MMP-9 levels.
Cepeda MA, Evered CL, Pelling JJH, Damjanovski S.
Cepeda MA, et al. Among authors: evered cl.
J Cell Commun Signal. 2017 Jun;11(2):167-179. doi: 10.1007/s12079-016-0373-3. Epub 2017 Jan 9.
J Cell Commun Signal. 2017.
PMID: 28070797
Free PMC article.
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Stable expression of α1-antitrypsin Portland in MDA-MB-231 cells increased MT1-MMP and MMP-9 levels, but reduced tumour progression.
Willson JA, Muir CA, Evered CL, Cepeda MA, Damjanovski S.
Willson JA, et al. Among authors: evered cl.
J Cell Commun Signal. 2018 Jun;12(2):479-488. doi: 10.1007/s12079-017-0407-5. Epub 2017 Aug 29.
J Cell Commun Signal. 2018.
PMID: 28849349
Free PMC article.
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