Dijoux Marie-Geneviève, Schnabel Peter C, Hallock Yali F, Boswell Jamie L, Johnson Tanya R, Wilson Jennifer A, Ireland Chris M, van Soest Rob, Boyd Michael R, Barrows Louis R, Cardellina John H
Laboratory of Drug Discovery Research and Development, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute-Frederick Cancer Research & Development Center, Frederick, MD 21702-1201, USA.
Bioorg Med Chem. 2005 Nov 1;13(21):6035-44. doi: 10.1016/j.bmc.2005.06.019.
A detailed analysis of four different collections of the sponge genus Zyzzya yielded nine pyrroloiminoquinones of the makaluvamine, batzelline, and isobatzelline/damirone classes. Dereplication analyses of additional Zyzzya extracts did not disclose more potent or additional new compounds. Comparative testing of these compounds in the National Cancer Institute's 60 cell line human tumor screen revealed varying levels of potency and differential cytotoxicity, apparently related to the unsaturation levels in and substitution patterns on the core ring system. Further studies on the topoisomerase II-mediated DNA cleavage were conducted. Reductive activation of the pyrroloiminoquinones led to DNA damage in vitro, which correlated with half wave potentials and reversibility parameters. DNA damage could be abrogated by ascorbate. Fluorescence displacement was used to measure intercalation with DNA; intercalation efficiency did not correlate with DNA-damaging proficiency. Makaluvamine H (5) emerged as the most potent and differential of our isolates, roughly comparable to makaluvamines C (in vitro) and I (in vivo). 3,7-Dimethyl guanine was isolated from one of the Zyzzya collections and from the sponge Latrunculia purpurea.
对海绵动物Zyzzya属的四个不同样本进行详细分析后,得到了9种属于makaluvamine、batzelline和异batzelline/damirone类别的吡咯并咪唑醌。对其他Zyzzya提取物进行的去重复分析未发现更具活性的或其他新化合物。在国立癌症研究所的60细胞系人类肿瘤筛选试验中对这些化合物进行比较测试,结果显示其活性水平各异且具有不同的细胞毒性,这显然与核心环系统中的不饱和水平和取代模式有关。还对拓扑异构酶II介导的DNA裂解进行了进一步研究。吡咯并咪唑醌的还原激活在体外导致DNA损伤,这与半波电位和可逆性参数相关。抗坏血酸盐可消除DNA损伤。采用荧光位移法测量与DNA的嵌入情况;嵌入效率与DNA损伤能力不相关。Makaluvamine H(5)是我们分离得到的化合物中活性最强且具有差异性的,大致与makaluvamines C(体外)和I(体内)相当。从Zyzzya的一个样本以及海绵Latrunculia purpurea中分离出了3,7-二甲基鸟嘌呤。