Antunovic Maja, Kriznik Bojana, Ulukaya Engin, Yilmaz Veysel T, Mihalic Katarina C, Madunic Josip, Marijanovic Inga
aDepartment of Molecular Biology, Division of Biology, Faculty of Science, University of Zagreb, Zagreb, Croatia bDepartment of Medical Biochemistry, Faculty of Medicine cDepartment of Chemistry, Faculty of Sciences, Uludag University, Bursa, Turkey.
Anticancer Drugs. 2015 Feb;26(2):180-6. doi: 10.1097/CAD.0000000000000174.
Effective treatment methods for human leukemia are under development, but so far none of them have been found to be completely satisfactory. It was recently reported that palladium complexes have significant anticancer activity as well as lower toxicity compared with some clinically used chemotherapeutics. The anticancer activities of two novel palladium(II) complexes, Pd(sac)(terpy)·4H2O and PdCl(terpy)·2H2O, were tested against three human leukemia cell lines, Jurkat, MOLT-4, and THP-1, in comparison with cisplatin and adriamycin. The cytotoxic effect of the drugs was determined using the MTT assay. Cell death was assessed using fluorescein isothiocyanate-annexin/propidium iodide staining for flow cytometry. Furthermore, p53 phosphorylation, poly(ADP-ribose) polymerase cleavage, and Bax and Bcl-2 mRNA levels were examined to elucidate the mechanism of cell death induction. Both complexes exhibited a significant dose-dependent antigrowth effect in vitro. The complexes predominately induced apoptosis, but necrosis was also observed. In-vitro results have shown that palladium(II) complexes may be regarded as potential anticancer agents for treating human leukemia. Therefore, further analysis to determine the putative mechanism of action and in-vivo studies on animal models are warranted.
人类白血病的有效治疗方法正在研发中,但目前尚未发现任何一种方法能完全令人满意。最近有报道称,与一些临床使用的化疗药物相比,钯配合物具有显著的抗癌活性且毒性较低。测试了两种新型钯(II)配合物Pd(sac)(terpy)·4H₂O和PdCl(terpy)·2H₂O对三种人类白血病细胞系Jurkat、MOLT - 4和THP - 1的抗癌活性,并与顺铂和阿霉素进行比较。使用MTT法测定药物的细胞毒性作用。使用异硫氰酸荧光素 - 膜联蛋白/碘化丙啶染色进行流式细胞术评估细胞死亡情况。此外,检测p53磷酸化、聚(ADP - 核糖)聚合酶裂解以及Bax和Bcl - 2 mRNA水平以阐明细胞死亡诱导机制。两种配合物在体外均表现出显著的剂量依赖性抗生长作用。这些配合物主要诱导细胞凋亡,但也观察到了坏死现象。体外研究结果表明,钯(II)配合物可被视为治疗人类白血病的潜在抗癌药物。因此,有必要进一步分析其假定的作用机制并在动物模型上进行体内研究。