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Pericellular proteolysis in cancer.

作者信息

Sevenich Lisa, Joyce Johanna A

机构信息

Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, New York, 10065, USA.

Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, New York, 10065, USA

出版信息

Genes Dev. 2014 Nov 1;28(21):2331-47. doi: 10.1101/gad.250647.114.


DOI:10.1101/gad.250647.114
PMID:25367033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4215179/
Abstract

Pericellular proteases have long been associated with cancer invasion and metastasis due to their ability to degrade extracellular matrix components. Recent studies demonstrate that proteases also modulate tumor progression and metastasis through highly regulated and complex processes involving cleavage, processing, or shedding of cell adhesion molecules, growth factors, cytokines, and kinases. In this review, we address how cancer cells, together with their surrounding microenvironment, regulate pericellular proteolysis. We dissect the multitude of mechanisms by which pericellular proteases contribute to cancer progression and discuss how this knowledge can be integrated into therapeutic opportunities.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/74c591181760/2331fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/085412585fe1/2331fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/4df6515e29f8/2331fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/74c591181760/2331fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/085412585fe1/2331fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/4df6515e29f8/2331fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b4/4215179/74c591181760/2331fig3.jpg

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本文引用的文献

[1]
Distinct functions of macrophage-derived and cancer cell-derived cathepsin Z combine to promote tumor malignancy via interactions with the extracellular matrix.

Genes Dev. 2014-10-1

[2]
Invadopodia are required for cancer cell extravasation and are a therapeutic target for metastasis.

Cell Rep. 2014-9-11

[3]
Loss of the Timp gene family is sufficient for the acquisition of the CAF-like cell state.

Nat Cell Biol. 2014-8-24

[4]
The androgen-regulated protease TMPRSS2 activates a proteolytic cascade involving components of the tumor microenvironment and promotes prostate cancer metastasis.

Cancer Discov. 2014-11

[5]
Analysis of tumour- and stroma-supplied proteolytic networks reveals a brain-metastasis-promoting role for cathepsin S.

Nat Cell Biol. 2014-9

[6]
Genome-wide identification of miR-200 targets reveals a regulatory network controlling cell invasion.

EMBO J. 2014-7-28

[7]
Extracellular matrix signatures of human primary metastatic colon cancers and their metastases to liver.

BMC Cancer. 2014-7-18

[8]
Legumain protease-activated TAT-liposome cargo for targeting tumours and their microenvironment.

Nat Commun. 2014-6-27

[9]
Network analyses reveal pervasive functional regulation between proteases in the human protease web.

PLoS Biol. 2014-5-27

[10]
IGF binding proteins in cancer: mechanistic and clinical insights.

Nat Rev Cancer. 2014-4-10

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