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Role of Matrix Metalloproteases in Degradation of ECM01:23

Role of Matrix Metalloproteases in Degradation of ECM

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Matrix metalloproteases (MMPs) are enzymes involved in the hydrolysis of proteins and glycoproteins of the extracellular matrix. MMPs are essential for the migration and proliferation of cells through the dense matrix network, throughout embryonic development, and throughout morphogenesis. The first MMP activity discovered was a collagenase in a tadpole's tail undergoing metamorphosis. The active collagen deposition and modifications lead to the morphogenesis of tadpoles into the adult...
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Translocation of Proteins into the Mitochondria01:19

Translocation of Proteins into the Mitochondria

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Mitochondrial precursors are translocated to the internal subcompartments via independent mechanisms involving distinct protein machineries called translocases.
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
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Metastasis02:30

Metastasis

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Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
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The Tumor Microenvironment02:17

The Tumor Microenvironment

6.3K
Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
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Cancer Cell Migration through Invadopodia01:35

Cancer Cell Migration through Invadopodia

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Invadosome is a broad category of cell surface structures with proteolytic activity that  degrades the extracellular matrix (ECM). Invadosomes are present in normal cell types, including macrophages, endothelial cells, and neurons, as well as tumor cells. Although the macrophage podosomes and tumor cell invadopodia are classified as invadosomes, they have different structures, molecular pathways, and functions. Podosomes are short structures that last for a few minutes. However,...
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Related Experiment Video

Updated: May 3, 2026

Experimental Metastasis Assay
08:28

Experimental Metastasis Assay

Published on: August 24, 2010

20.3K

Metalloproteinases in melanoma.

Nives Moro1, Cornelia Mauch1, Paola Zigrino1

  • 1Department of Dermatology and Venerology, University of Cologne, Germany.

European Journal of Cell Biology
|February 18, 2014
PubMed
Summary

Matrix metalloproteinases (MMPs) and ADAMs are key proteases in melanoma invasion. Their activity remodels the extracellular matrix and influences tumour cell communication, promoting cancer spread.

Area of Science:

  • Oncology
  • Biochemistry

Background:

  • Tumour cell adhesion, motility, and proteolytic activities are crucial for cancer invasion.
  • Melanoma invasion involves progression from epidermis to distant organs via blood or lymphatic vessels.
  • Proteolytic enzymes play a pivotal role in promoting melanoma cell invasion.

Purpose of the Study:

  • To summarize current knowledge on the role of metalloproteinases, specifically matrix metalloproteinases (MMPs) and disintegrin and metalloproteinases (ADAMs), in melanoma invasion.

Main Methods:

  • Review of existing literature on the function of proteases in melanoma.
  • Analysis of the roles of MMPs and ADAMs in extracellular matrix remodeling.
  • Examination of how these enzymes influence cell-microenvironment interactions.
Keywords:
ADAMMMPMelanomaMetastasisProteases

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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
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Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
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Related Experiment Videos

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Experimental Metastasis Assay
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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis

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Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
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Main Results:

  • Proteolytic enzymes, including MMPs and ADAMs, are essential for melanoma cell invasion.
  • These enzymes remodel the extracellular matrix, facilitating tumour cell movement.
  • They also release active factors and shed cell surface receptors, mediating melanoma cell communication.

Conclusions:

  • MMPs and ADAMs are critical mediators of melanoma invasion and metastasis.
  • Understanding their functions is key to developing targeted therapies.
  • Targeting these metalloproteinases could inhibit melanoma progression.