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Hypoxia-directed and activated theranostic agent: Imaging and treatment of solid tumor

Authors
Kumar, RajeshKim, Eun-JoongHan, JiyouLee, HyunseungShin, Weon SupKim, Hyun MinBhuniya, SankarprasadKim, Jong SeungHong, Kwan Soo
Issue Date
10월-2016
Publisher
ELSEVIER SCI LTD
Keywords
Anti-tumor; Hypoxia; Prodrug; Solid tumor; Theranostic
Citation
BIOMATERIALS, v.104, pp.119 - 128
Indexed
SCIE
SCOPUS
Journal Title
BIOMATERIALS
Volume
104
Start Page
119
End Page
128
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/87259
DOI
10.1016/j.biomaterials.2016.07.010
ISSN
0142-9612
Abstract
Hypoxia, a distinguished feature of various solid tumors, has been considered as a key marker for tumor progression. Inadequate vasculature and high interstitial pressures result in relatively poor drug delivery to these tumors. Herein, we developed an antitumor theranostic agent, 4, which is activated in hypoxic conditions and can be used for the diagnosis and treatment of solid tumors. Compound 4, bearing biotin, a tumor-targeting unit, and SN38, an anticancer drug, proved to be an effective theranostic agent for solid tumors. SN38 plays a dual role: as an anticancer drug for therapy and as a fluorophore for diagnosis, thus avoids an extra fluorophore and limits cytotoxicity. Compound 4, activated in the hypoxic environment, showed high therapeutic activity in A549 and HeLa cells and spheroids. In vivo imaging of solid tumors confirmed the tumor-specific localization, deep tissue penetration and activation of compound 4, as well as the production of a strong anticancer effect through the inhibition of tumor growth in a xenograft mouse model validating it as a promising strategy for the treatment of solid tumors. (C) 2016 Elsevier Ltd. All rights reserved.
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