Myers C, Gianni L, Zweier J, Muindi J, Sinha B K, Eliot H
Fed Proc. 1986 Nov;45(12):2792-7.
Adriamycin forms a chelate with Fe(III) that exhibits complex redox chemistry. The drug ligand is able to directly reduce the bound Fe(III) with the concomitant production of a one-electron oxidized drug radical. This Fe(II) can reduce oxygen to hydrogen peroxide and cleave the peroxide to yield the hydroxyl radical. In addition, the drug X Fe complex can catalyze the transfer of electrons from reduced glutathione to molecular oxygen to yield superoxide, hydrogen peroxide, and hydroxyl radicals. The adriamycin X Fe complex binds to DNA to form a ternary drug X Fe X DNA complex, which is also able to catalyze the thiol-dependent reduction of oxygen and the formation of hydroxyl radical from hydrogen peroxide. As a consequence of this chemistry, the adriamycin X Fe complex can cleave DNA on the addition of glutathione or hydrogen peroxide. Although less well defined, the adriamycin X Fe complex can bind to cell membranes and cause oxidative destruction of these membranes in the presence of thiols or hydrogen peroxide.
阿霉素与Fe(III)形成一种螯合物,该螯合物呈现出复杂的氧化还原化学性质。药物配体能够直接还原结合的Fe(III),同时产生单电子氧化的药物自由基。这种Fe(II)可将氧气还原为过氧化氢,并裂解过氧化物生成羟基自由基。此外,药物 - Fe络合物可催化电子从还原型谷胱甘肽转移至分子氧,生成超氧化物、过氧化氢和羟基自由基。阿霉素 - Fe络合物与DNA结合形成三元药物 - Fe - DNA络合物,该络合物也能够催化硫醇依赖性的氧还原反应以及由过氧化氢形成羟基自由基。由于这种化学反应,在添加谷胱甘肽或过氧化氢时,阿霉素 - Fe络合物能够裂解DNA。虽然其作用机制尚不十分明确,但在存在硫醇或过氧化氢的情况下,阿霉素 - Fe络合物可与细胞膜结合并导致这些膜的氧化破坏。