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An Activatable Prodrug for the Treatment of Metastatic Tumors

Authors
Kim, Eun-JoongBhuniya, SankarprasadLee, HyunseungKim, Hyun MinCheong, ChaejoonMaiti, SukhenduHong, Kwan SooKim, Jong Seung
Issue Date
1-10월-2014
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.136, no.39, pp.13888 - 13894
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume
136
Number
39
Start Page
13888
End Page
13894
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/97129
DOI
10.1021/ja5077684
ISSN
0002-7863
Abstract
Metastatic cancers have historically been difficult to treat. However, metastatic tumors have been found to have high levels of reactive oxygen species such as hydrogen peroxide (H2O2), supporting the hypothesis that a prodrug could be activated by intracellular H2O2 and lead to a potential antimetastatic therapy. In this study, prodrug 7 was designed to be activated by H2O2-mediated boronate oxidation, resulting in activation of the fluorophore for detection and release of the therapeutic agent, SN-38. Drug release from prodrug 7 was investigated by monitoring fluorescence after addition of H2O2 to the cancer cells. Prodrug 7 activated by H2O2 selectively inhibited tumor cell growth. Furthermore, intratracheally administered produrg 7 showed effective antitumor activity in a mouse model of metastatic lung disease. Thus, this H2O2-responsive prodrug has therapeutic potential as a novel treatment for metastatic cancer via cellular imaging with fluorescence as well as selective release of the anticancer drug, SN-38.
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