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Selective Activation of a Prodrug by Thioredoxin Reductase Providing a Strategy to Target Cancer Cells
Author(s) -
Li Xinming,
Hou Yanan,
Meng Xianke,
Ge Chunpo,
Ma Huilong,
Li Jin,
Fang Jianguo
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201801058
Subject(s) - thioredoxin reductase , prodrug , selenocysteine , selenoprotein , chemistry , thioredoxin , cancer cell , gemcitabine , reactive oxygen species , biochemistry , enzyme , cancer , microbiology and biotechnology , cancer research , biology , glutathione , cysteine , glutathione peroxidase , genetics
Elevated reactive oxygen species and antioxidant defense systems have been recognized as one of the hallmarks of cancer cells. As a major regulator of the cellular redox homeostasis, the selenoprotein thioredoxin reductase (TrxR) is increasingly considered as a promising target for anticancer drug development. The current approach to inhibit TrxR predominantly relies on the modification of the selenocysteine residue in the C‐terminal active site of the enzyme, in which it is hard to avoid the off‐target effects. By conjugating the anticancer drug gemcitabine with a 1,2‐dithiolane scaffold, an unprecedented prodrug strategy is disclosed that achieves a specific release of gemcitabine by TrxR in cells. As overexpression of TrxR is frequently found in different types of tumors, the TrxR‐dependent prodrugs are promising for further development as cancer chemotherapeutic agents.