Target intelligence / Profile preview

Matrix metalloproteinases and A disintegrin and metalloproteinases (MMPs and ADAMs) (MMPs and ADAMs)

Target
MMPs and ADAMs
Molecular classification
Enzyme, Metalloproteinase, Protease
01

Overview

Matrix metalloproteinases (MMPs) and A Disintegrin and Metalloproteinases (ADAMs) are two families of zinc-dependent endopeptidases that are essential for the modification of the extracellular environment and the regulation of cell-surface protein signaling. MMPs, also known as matrixins, primarily function to degrade and remodel various components of the extracellular matrix (ECM), such as collagen, elastin, and fibronectin, which is critical for physiological processes like wound healing, bone development, and angiogenesis (Source: PubMed, PMID: 28273522). ADAMs, or adamalysins, are transmembrane proteins that facilitate 'ectodomain shedding,' the process of releasing the extracellular portions of membrane-bound proteins, including cytokines like TNF-alpha and growth factors like TGF-alpha, thereby modulating diverse signaling pathways (Source: UniProt, P78536). In disease states, the overactivity of these enzymes is linked to cancer metastasis, where they promote tumor invasion, as well as chronic inflammatory conditions and cardiovascular diseases (Source: NIH, 'Matrix Metalloproteinases in Health and Disease'). While they represent significant therapeutic targets, the clinical development of broad-spectrum inhibitors has been hindered by severe side effects, most notably musculoskeletal syndrome (MSS), which causes debilitating joint pain and stiffness (Source: Nature Reviews Drug Discovery, doi:10.1038/nrd745). Consequently, current research focuses on the development of highly selective inhibitors that can target specific disease-associated isoforms while sparing those necessary for normal tissue homeostasis.

Other names
MatrixinsAdamalysinsMetalloproteinasesMMP familyADAM familyZinc-dependent metalloproteinases
02

Mechanism of action

Inhibition of the zinc-dependent catalytic domain to prevent the proteolytic cleavage of extracellular matrix components or the shedding of cell-surface signaling molecules (Source: PubMed, PMID: 12069711).

03

Biological functions

Extracellular matrix degradationTissue remodelingEctodomain sheddingCell signalingAngiogenesisCell migration
04

Disease associations

CancerInflammationArthritisCardiovascular diseaseNeurodegenerative disease
05

Safety considerations

Musculoskeletal syndrome (MSS)Joint pain and stiffnessLack of isoform selectivitySystemic toxicityImpaired wound healing
06

Interacting drugs

Marimastat

8 more in the full profile.

07

Biomarkers

MMP-2MMP-9TIMP-1C-terminal telopeptide of type I collagen (CTX-I)Soluble TNF-alpha

Beyond the preview

Go deeper on Matrix metalloproteinases and A disintegrin and metalloproteinases (MMPs and ADAMs) (MMPs and ADAMs).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Matrix metalloproteinases and A disintegrin and metalloproteinases (MMPs and ADAMs) (MMPs and ADAMs).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call