Tse-Dinh Y C, McGee L R
Biochem Biophys Res Commun. 1987 Mar 30;143(3):808-12. doi: 10.1016/0006-291x(87)90320-2.
Gilvocarcins are antitumor agents that have been reported to damage DNA upon activation by visible light. This activation is dependent on interaction with DNA. Here it is shown that gilvocarcin V and its synthetic aglycone analogue can both introduce single-strand scission into plasmid DNA. Light irradiation is required for the reaction. The binding of gilvocarcin V to plasmid DNA in the absence of light decreased the DNA linking number in a fashion similar to known intercalating agents such as ethidium bromide. The use of oligonucleotides as substrates for gilvocarcin V demonstrated that one of the steps of the reaction following binding of gilvocarcin V to DNA involves covalent modification at thymidine and to a lesser extent, cytosine residues.
吉尔vocarcin是一类抗肿瘤药物,据报道,其在可见光激活后会损伤DNA。这种激活依赖于与DNA的相互作用。本文表明,吉尔vocarcin V及其合成苷元类似物均可使质粒DNA产生单链断裂。该反应需要光照。在无光条件下,吉尔vocarcin V与质粒DNA的结合以类似于已知嵌入剂(如溴化乙锭)的方式降低了DNA的连环数。以寡核苷酸作为吉尔vocarcin V的底物表明,吉尔vocarcin V与DNA结合后反应的其中一个步骤涉及对胸腺嘧啶核苷的共价修饰,对胞嘧啶残基的修饰程度较小。