Laboratory of Molecular Pharmacology and Experimental Chemotherapy, Department of Pharmacology, Pharmacotherapy, and Toxicology, Faculty of Pharmacy, Medical University of Sofia, 2 Dunav Street, 1000 Sofia, Bulgaria.
Bioinorg Chem Appl. 2008;2008:367471. doi: 10.1155/2008/367471.
The antineoplastic potential of a stable monomeric Au(II) complex with hematoporphyrin IX (Hp), namely [Au(II)Hp(-2H).(H(2)O)(2)], was investigated in a panel of tumor cell lines. The complex exhibits strong cytotoxicity, whereby the leukaemia- and lymphoma-derived cell lines are more sensitive, with IC(50) values comparable to those of the reference anticancer drug cisplatin. In contrast, the solid tumor models are more sensitive to the platinum drug. A comparative assessment of both agents against the human kidney cell line 293T has shown that [Au(II)Hp(-2H).(H(2)O)(2)] is less cytotoxic. The gold complex induces oligonucleosomal DNA fragmentation in tumour cells following 24-hour treatment and hence its cytotoxic effect is at least partly mediated by induction of apoptotic cell death. A prominent intracellular gold accumulation was detected after treating tumor cells with [Au(II)Hp(-2H).(H(2)O)(2)] which shows that its putative pharmacological targets are readily accessible after a short incubation period.
我们研究了一种稳定的单核金(II)配合物与血卟啉 IX(Hp)的抗肿瘤潜力,即 [Au(II)Hp(-2H)。(H(2)O)(2)],在一系列肿瘤细胞系中进行了研究。该配合物表现出很强的细胞毒性,其中白血病和淋巴瘤衍生的细胞系更为敏感,IC(50)值与参考抗癌药物顺铂相当。相比之下,实体瘤模型对铂类药物更为敏感。对人肾细胞系 293T 进行的这两种药物的比较评估表明,[Au(II)Hp(-2H)。(H(2)O)(2)]的细胞毒性较小。金配合物在 24 小时治疗后诱导肿瘤细胞中的寡核苷酸体 DNA 片段化,因此其细胞毒性作用至少部分是通过诱导细胞凋亡死亡介导的。在用 [Au(II)Hp(-2H)。(H(2)O)(2)]处理肿瘤细胞后,检测到明显的细胞内金积累,这表明其潜在的药理靶标在短孵育期后即可轻易到达。