ER-resident oxidoreductases are glycosylated and trafficked to the cell surface to promote matrix degradation by tumour cells-Reference-Cited by-同舟云学术

ER-resident oxidoreductases are glycosylated and trafficked to the cell surface to promote matrix degradation by tumour cells

Published:2020-10-19 Issue:11 Volume:22 Page:1371-1381
ISSN:1465-7392
Container-title:Nature Cell Biology
language:en
Short-container-title:Nat Cell Biol

Author:

Ros Manon,Nguyen Anh Tuan,Chia Joanne,Le Tran Son,Le Guezennec Xavier,McDowall Ruth,Vakhrushev Sergey^ORCID,Clausen Henrik^ORCID,Humphries Martin James^ORCID,Saltel Frederic,Bard Frederic André^ORCID

Funder

Cancer Research UK

Fondation pour la Recherche Médicale

Agency for Science, Technology and Research

Integrated Cancer Research

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

Link

https://www.nature.com/articles/s41556-020-00590-w.pdf

Reference62 articles.

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3. Hotary, K., Allen, E., Punturieri, A., Yana, I. & Weiss, S. J. Regulation of cell invasion and morphogenesis in a three-dimensional type I collagen matrix by membrane-type matrix metalloproteinases 1, 2, and 3. J. Cell Biol. 149, 1309–1323 (2000).

4. Hotary, K. B. et al. Membrane type I matrix metalloproteinase usurps tumor growth control imposed by the three-dimensional extracellular matrix. Cell 114, 33–45 (2003).

5. Nguyen, A. T. et al. Organelle specific O-glycosylation drives MMP14 activation, tumor growth, and metastasis. Cancer Cell 32, 639–653.e6 (2017).

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