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抗肿瘤醌类物质引发的自由基形成

Free radical formation by antitumor quinones.

作者信息

Powis G

机构信息

Department of Pharmacology, Mayo Clinic & Foundation, Rochester, MN 55905.

出版信息

Free Radic Biol Med. 1989;6(1):63-101. doi: 10.1016/0891-5849(89)90162-7.

Abstract

Quinones are among the most frequently used drugs to treat human cancer. All of the antitumor quinones can undergo reversible enzymatic reduction and oxidation, and form semiquinone and oxygen radicals. For several antitumor quinones enzymatic reduction also leads to formation of alkylating species but whether this involves reduction to the semiquinone or the hydroquinone is not always clear. The antitumor activity of quinones is frequently linked to DNA damage caused by alkylating species or oxygen radicals. Some other effects of the antitumor quinones, such as cardiotoxicity and skin toxicity, may also be related to oxygen radical formation. The evidence for a relationship between radical formation and the biological activity of the antitumor quinones is evaluated.

摘要

醌类是治疗人类癌症最常用的药物之一。所有抗肿瘤醌类都能进行可逆的酶促还原和氧化,并形成半醌和氧自由基。对于几种抗肿瘤醌类,酶促还原还会导致烷基化物质的形成,但这是涉及还原为半醌还是对苯二酚并不总是清楚。醌类的抗肿瘤活性通常与烷基化物质或氧自由基引起的DNA损伤有关。抗肿瘤醌类的一些其他作用,如心脏毒性和皮肤毒性,也可能与氧自由基的形成有关。本文评估了自由基形成与抗肿瘤醌类生物活性之间关系的证据。

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