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拓扑异构酶II依赖性新型抗肿瘤化合物美罗西尔和美罗丹托因可诱导Daudi细胞凋亡。

Topoisomerase II-dependent novel antitumor compounds merocil and merodantoin induce apoptosis in Daudi cells.

作者信息

Gulliya K S, Franck B, Schneider U, Sharma R, Arnold L, Matthews J L

机构信息

Baylor Research Institute, Dallas, TX 75226.

出版信息

Anticancer Drugs. 1994 Oct;5(5):557-66. doi: 10.1097/00001813-199410000-00007.

Abstract

Three photoproducts of merocyanine 540 have been isolated, chemically characterized and synthesized. Two of these photoproducts, merocil and merodantoin, show significant antitumor activity in vitro and in vivo while demonstrating minimal toxicity to normal cells and tissues. Treatment of lymphoma cells with these compounds resulted in a rapid decline in macromolecular synthesis, DNA fragmentation inhibitable by actinomycin D and cycloheximide, and a marked rise in intracellular calcium. In vitro analysis revealed that activity of these compounds is dependent on topoisomerase II. These results are discussed in terms of the novel class of topoisomerase II-dependent compounds for potential use in chemotherapy.

摘要

部花青540的三种光产物已被分离、进行化学表征并合成。其中两种光产物,部花青和部花青二酮,在体外和体内均表现出显著的抗肿瘤活性,同时对正常细胞和组织的毒性极小。用这些化合物处理淋巴瘤细胞导致大分子合成迅速下降、放线菌素D和环己酰亚胺可抑制的DNA片段化以及细胞内钙显著升高。体外分析表明,这些化合物的活性依赖于拓扑异构酶II。就用于化疗的新型拓扑异构酶II依赖性化合物对这些结果进行了讨论。

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