posted on 2014-06-26, 00:00authored byYaping Liu, Dongzhu Duan, Juan Yao, Baoxin Zhang, Shoujiao Peng, HuiLong Ma, Yanlin Song, Jianguo Fang
The
selenoprotein thioredoxin reductase (TrxR) plays a pivotal
role in regulating cellular redox homeostasis and has attracted increasing
attention as a promising anticancer drug target. We report here that
2-(4-aminophenyl)-1,3,2-dithiarsinane (PAO–PDT, 4), a potent and highly selective small molecule inhibitor of TrxR,
stoichiometrically binds to the C-terminal selenocysteine/cysteine
pair in the enzyme in vitro and induces oxidative stress-mediated
apoptosis in HL-60 cells. The molecular action of 4 in
cells involves inhibition of TrxR, elevation of reactive oxygen species,
depletion of cellular thiols, and activation of caspase-3. Knockdown
of TrxR sensitizes the cells to 4 treatment, whereas
overexpression of the functional enzyme alleviates the cytotoxicity,
providing physiological relevance for targeting TrxR by 4 in cells. The simplicity of the structure and the presence of an
easily manipulated amine group will facilitate the further development
of 4 as a potential cancer chemotherapeutic agent.