Role of Matrix Metalloproteinases in Photoaging and Photocarcinogenesis
Open accessAbstract
Matrix metalloproteinases (MMPs) are zinc-containing endopeptidases with an extensive range of substrate specificities. Collectively, these enzymes are able to degrade various components of extracellular matrix (ECM) proteins. Based on their structure and substrate specificity, they can be categorized into five main subgroups, namely (1) collagenases (MMP-1, MMP-8 and MMP-13); (2) gelatinases (MMP-2 and MMP-9); (3) stromelysins (MMP-3, MMP-10 and MMP-11); (4) matrilysins (MMP-7 and MMP-26); and (5) membrane-type (MT) MMPs (MMP-14, MMP-15, and MMP-16). The alterations made to the ECM by MMPs might contribute in skin wrinkling, a characteristic of premature skin aging. In photocarcinogenesis, degradation of ECM is the initial step towards tumor cell invasion, to invade both the basement membrane and the surrounding stroma that mainly comprises fibrillar collagens. Additionally, MMPs are involved in angiogenesis, which promotes cancer cell growth and migration. In this review, we focus on the present knowledge about premature skin aging and skin cancers such as basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and melanoma, with our main focus on members of the MMP family and their functions.
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MMPs, particularly gelatinases (MMP-2 and -9), are the major enzymes responsible for degradation of the extracellular matrix containing collagen and gelatin.
“MMPs, in particular gelatinases (MMP-2 and -9) that cleave soluble type-IV and type-I collagen, represent the major enzymes responsible for the degradation of the extracellular matrix which contains diverse biomolecules including collagen and gelatin (Figure 4) [56].”
From Licorice (Glycyrrhiza glabra, G. uralensis, and G. inflata) and Their Constituents as Active Cosmeceutical Ingredients (2022) · cites this paper as [56]
Exposure of human skin to ROS through factors including UV enhances MMP activity associated with breakdown of collagen fibers.
“Exposure of human skin to ROS (reactive oxygen species) through several factors, including UV, has been reported to enhance matrix metalloproteinases (MMPs) activity associated with a notable breakdown of collagen fibers.”
From Licorice (Glycyrrhiza glabra, G. uralensis, and G. inflata) and Their Constituents as Active Cosmeceutical Ingredients (2022) · cites this paper as [56]
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- Authors
- Pittayapruek, P., Meephansan, J., Prapapan, O., Komine, M., & Ohtsuki, M.
- Affiliations
- Thammasat University (TH)
- Jichi Medical University (JP)
- Corresponding author
- Komine, Mayumi
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2016-06-02
- Volume
- 17
- Issue
- 6
- Pages
- 868
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC4926402
- OpenAlex
- W2409710963
- Cited by
- 1,099
- References
- 101
- Citations by year
- 2026: 99 · 2025: 116 · 2024: 143 · 2023: 158 · 2022: 181 · 2021: 130 · 2020: 105 · 2019: 87 · 2018: 47 · 2017: 30 · 2016: 3
- FWCI
- 5.06
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Thailand Research Fund (TRG5780230)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Keywords
- matrix metalloproteinases, photoaging, photocarcinogenesis, extracellular matrix degradation, collagenase, gelatinase, stromelysin, matrilysin, membrane-type MMPs, skin cancer, basal cell carcinoma, squamous cell carcinoma, melanoma, tumor invasion, angiogenesis, skin wrinkling
- MeSH terms
- Aging, Animals, Cell Transformation, Neoplastic, Humans, Neoplasms, Ultraviolet Rays, Reactive Oxygen Species, Matrix Metalloproteinases
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