Aramvash Asieh, Rabbani Chadegani Azra, Lotfi Safa
Department of Biochemistry, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.
Department of Bioscience and Biotechnology, Malek-Ashtar University of Technology, Tehran, Iran.
Iran J Pharm Res. 2017 Summer;16(3):1204-1213.
Anthracycline antibiotics are potent anticancer drugs widely used in the treatment of solid tumors and hematological malignancies. Because of their extensive clinical use and their toxic effect on normal cells, in the present study the effect of these drugs on multipotent hematopoietic bone marrow cells was investigated employing, viability tests, PARP cleavage, Hoechst 33258 staining, DNA fragmentation and superoxide anion production techniques. The results revealed that daunorubicin and doxorubicin exhibited time and dose dependent cytotoxicity against the cells and upon increasing the drugs concentrations, apoptosis was occurred after 4 h of incubation and at low concentration of the drugs. The cleavage of poly ADP-ribose polymerase (PARP) demonstrated by daunorubicin and doxorubicin treatment of the cells, suggest that the apoptotic process is PARP dependent. The drugs induced DNA fragmentation and also anion superoxide production was increased upon rising drugs concentrations. From the results it is concluded that anthracycline antibiotics represent cytotoxic effect on hematopoietic progenitor/stem cells of bone marrow, inducing apoptosis and in this process toxicity of daunorubicin is more pronounced compared to doxorubicin.
蒽环类抗生素是强效抗癌药物,广泛用于实体瘤和血液系统恶性肿瘤的治疗。由于其广泛的临床应用以及对正常细胞的毒性作用,在本研究中,采用活力测试、PARP裂解、Hoechst 33258染色、DNA片段化和超氧阴离子产生技术,研究了这些药物对多能造血骨髓细胞的影响。结果显示,柔红霉素和阿霉素对细胞表现出时间和剂量依赖性细胞毒性,随着药物浓度增加,孵育4小时后以及在低药物浓度下发生凋亡。柔红霉素和阿霉素处理细胞后显示的聚ADP-核糖聚合酶(PARP)裂解表明,凋亡过程是PARP依赖性的。药物诱导DNA片段化,并且随着药物浓度升高,超氧阴离子产生也增加。从结果得出结论,蒽环类抗生素对骨髓造血祖细胞/干细胞具有细胞毒性作用,诱导凋亡,并且在此过程中,柔红霉素的毒性比阿霉素更明显。