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Updated: Jul 3, 2026

Measuring Global Cellular Matrix Metalloproteinase and Metabolic Activity in 3D Hydrogels
Published on: January 22, 2019
Dysregulation of matrix metalloproteinases and their tissue inhibitors by S100A4
Renate Elenjord1, Hilde Ljones, Elisabeth Sundkvist
1Department of Pharmacy, University of Tromsø, Tromsø, Norway. renate.elenjord@farmasi.uit.no
Abstract:
The S100A4 protein as well as the matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) are associated with diseases such as arthritis and cancer. This mini review focuses on in vitro and in vivo studies indicating S100A4 involvement in regulation of MMPs and TIMPs, and the biological and pathobiological consequences of this regulation.
Insights
The S100A4 protein regulates matrix metalloproteinases (MMPs) and tissue inhibitors (TIMPs), impacting diseases like arthritis and cancer. This review explores S100A4
Area of Science:
- Biochemistry
- Molecular Biology
- Pathology
Background:
- S100A4 protein, matrix metalloproteinases (MMPs), and tissue inhibitors of metalloproteinases (TIMPs) are implicated in various diseases.
- Dysregulation of MMPs and TIMPs is a hallmark of pathological conditions including arthritis and cancer.
- The precise role of S100A4 in modulating MMPs and TIMPs requires further elucidation.
Purpose of the Study:
- To review in vitro and in vivo studies investigating the regulatory role of S100A4 on MMPs and TIMPs.
- To summarize the biological and pathobiological consequences stemming from S100A4-mediated regulation of MMPs and TIMPs.
- To consolidate current knowledge on S100A4's function in disease pathogenesis.
Main Methods:
- Comprehensive literature search of in vitro and in vivo studies.
- Analysis of experimental data linking S100A4 to MMP and TIMP expression and activity.
- Synthesis of findings regarding the functional outcomes of S100A4-MMP/TIMP interactions.
Main Results:
- Evidence demonstrates S100A4's involvement in the regulation of specific MMPs and TIMPs.
- S100A4 influences cellular processes critical to disease progression, such as invasion and inflammation.
- The interplay between S100A4, MMPs, and TIMPs contributes to the pathogenesis of arthritis and cancer.
Conclusions:
- S100A4 plays a significant role in controlling the MMP/TIMP balance.
- This regulation by S100A4 has direct implications for disease development and progression.
- Targeting the S100A4-MMP/TIMP axis presents potential therapeutic strategies for S100A4-associated diseases.
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