Stimulus-responsive nanoscale delivery systems triggered by the enzymes in the tumor microenvironment
Abstract
The tumor microenvironment is the cellular environment that is also described as the "soil" for supporting tumor growth, proliferation, invasion and metastasis, as well as protecting tumor cells from immunological recognition. Notably, tumor cells can grow much faster than other normal organs and invade surrounding tissues more easily, which results in abnormal expression of enzymes in the tumor microenvironment, including matrix metalloproteinases, cathepsins, phospholipases, oxidoreductases, etc. In opposite, due to the high selectivity and catalytic activity, these enzymes can promote nanoparticles to recognize tumor tissues more accurately, and the more accumulation of drugs at primal tumor sites will enhance therapeutic efficacy with lower systemic toxicity. Therefore, one promising antitumor strategy is to design stimulus-responsive nanoscale delivery systems triggered by the enzymes with the support of various nanocarriers, such as liposomes, micelles and inorganic nanoparticles, etc. In this review, numerous facts were cited to summarize and discuss the typical types of enzyme-stimulus responsive nanoscale delivery systems. More importantly, we also focused on their recent advancements in antitumor therapy, and offered the direction for further studies.
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The tumor microenvironment exhibits aberrant expression of enzymes such as matrix metalloproteinases, cathepsins, phospholipases, and oxidoreductases because tumor cells grow more quickly than other normal organs and require more enzymes for functional support.
“The tumor microenvironment exhibits aberrant expression of enzymes such as matrix metalloproteinases, cathepsins, phospholipases, and oxidoreductases because tumor cells grow more quickly than other normal organs and require more enzymes for functional support.142”
From Smart nanoparticles for cancer therapy (2023) · cites this paper as [142]
The binding of uPA and its receptor (uPAR) helps activate the serine protease plasminogen to become plasmin, starting a series of proteolytic cascade reactions to break down the extracellular matrix's components and encourage tumor invasion and metastasis.
“The binding of uPA and its receptor (uPAR) will help activate the serine protease plasminogen to become plasmin. Afterwards, start a series of proteolytic cascade reactions to break down the extracellular matrix’s components and encourage tumor invasion and metastasis.142,151”
From Smart nanoparticles for cancer therapy (2023) · cites this paper as [142]
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References 111 · Cited by 82
- Authors
- Zhang, Z.-T., Huang-Fu, M.-Y., Xu, W.-H., & Han, M.
- Affiliations
- Zhejiang University (CN)
- Corresponding author
- Han, Min
- ORCID
- Han, Min
- Venue
- European Journal of Pharmaceutics and Biopharmaceutics
- Publisher
- Elsevier BV
- Published
- 2019-04
- Volume
- 137
- Pages
- 122-130
- ISSN
- 0939-6411 (ISSN-L)
- OpenAlex
- W2912934007
- Cited by
- 82
- References
- 111
- Citations by year
- 2026: 11 · 2025: 12 · 2024: 6 · 2023: 16 · 2022: 16 · 2021: 7 · 2020: 9 · 2019: 5
- FWCI
- 0.59
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- European Journal of Pharmaceutics and Biopharmaceutics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Basic Research Program of China (2014CB931901)
- National Natural Science Foundation of China (81673022, 81373346)
- Zhejiang Provincial Natural Science Foundation of China (LY17H160013, LY15H300001)
- Fundamental Research Funds for the Central Universities (2017XZZX011-04)
- Zhejiang Medical and Health Science and Technology Plan Project (2016KYB109)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Physical Sciences › Materials Science › Polymers and Plastics › Dendrimers and Hyperbranched Polymers
- Keywords
- enzyme-responsive drug delivery, tumor microenvironment, matrix metalloproteinases, cathepsins, liposomes, micelles, inorganic nanoparticles, targeted drug delivery, cancer therapy, enzyme-responsive drug release
- MeSH terms
- Animals, Antineoplastic Agents, Enzymes, Humans, Liposomes, Micelles, Neoplasms, Drug Delivery Systems, Nanoparticles, Tumor Microenvironment
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