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Cited 2 time in webofscience Cited 2 time in scopus
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Detection of lysyl oxidase activity in tumor extracellular matrix using peptide-functionalized gold nanoprobesopen access

Authors
Kim, Han YoungJo, MiheeLa, Ju A.Choi, YoungjinCho, Eun ChulKim, Su HeeJung, YoungmeeKim, KwangmeyungRyu, Ju Hee
Issue Date
Sep-2021
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
lysyl oxidase; gold nanoparticles; colorimetric assays; extracellular matrix; tumor stiffness
Citation
Cancers, v.13, no.18, pp 1 - 16
Pages
16
Indexed
SCIE
SCOPUS
Journal Title
Cancers
Volume
13
Number
18
Start Page
1
End Page
16
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/141019
DOI
10.3390/cancers13184523
ISSN
2072-6694
2072-6694
Abstract
High LOX levels in the tumor microenvironment causes the cross-linking of extracellular matrix components and increases the stiffness of tumor tissue. Thus, LOX plays an important role in tumorigenesis and in lowering the tumor response to anticancer drugs. Despite comprehensive efforts to identify the roles of LOX in the tumor microenvironment, sensitive and accurate detection methods have not yet been established. Here, we suggest the use of gold nanoparticles functionalized with LOX-sensitive peptides (LS-AuNPs) that aggregate upon exposure to LOX, resulting in a visual color change. LOX-sensitive peptides (LS-peptides) contain lysine residues that are converted to allysine in the presence of LOX, which is highly reactive and binds to adjacent allysine, resulting in the aggregation of the AuNPs. We demonstrated that the synthesized LS-AuNPs are capable of detecting LOX sensitively, specifically both in vitro and in the tissue extract. Moreover, the suggested LS-AuNP-based assay is more sensitive than commonly employed assays or commercially available kits. Therefore, the LS-AuNPs developed in this study can be used to detect LOX levels and can be further used to predict the stiffness or the anticancer drug resistance of the tumor.
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