N. Rajab, Zariyantey Abd Hamid, Hunaizah Hassan, A. Ali, L. Din, S. Inayat-Hussain
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引用次数: 21
摘要
采用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基- 2h -溴化四氮唑(MTT)试验和碱性彗星试验,分别对植物苯内酯goniothalamin在人白血病细胞系中的细胞毒性和基因毒性进行了评价。治疗72 h后,人HL-60早幼粒细胞白血病细胞和CEM-SS t淋巴母细胞中goniothalamin的IC50值分别为4.5 μg/mL和2.4 μg/mL。在IC10和IC25浓度下,早在处理后2小时,就检测到goniothalamin对HL-60和CEM-SS细胞的遗传毒性。然而,用抗氧化剂n -乙酰半胱氨酸(NAC)预处理1 mM 30分钟并不能消除该化合物的遗传毒性。这一结果表明,卵泡胺对DNA损伤的主要诱导可能不涉及氧化损伤。总之,我们的研究结果表明,在白血病细胞中,goniothalamin引起了基因毒性损伤。还需要进一步的研究来确定卵泡胺在诱导DNA损伤中的作用模式。
Evaluation of the cytotoxic and genotoxic effects of goniothalamin in leukemic cell lines
The cytotoxic and genotoxic effects of goniothalamin, a plant styryllactone, were evaluated using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay and the Alkaline Comet assay respectively in human leukemic cell lines. Following 72 h of treatment, the IC50 values of goniothalamin in human HL-60 promyelocytic leukemia cells and CEM-SS T-lymphoblastic cells were 4.5 μg/mL and 2.4 μg/mL respectively. The genotoxicity of goniothalamin in both HL-60 and CEM-SS cells was detected as early as 2 h following treatment at IC10 and IC25 concentrations. However, pretreatment with the antioxidant N-acetyl-cysteine (NAC) at 1 mM for 30 minutes did not abrogate genotoxicity of this compound. This result suggests that primary induction of DNA damage by goniothalamin may not involve oxidative damage. In conclusion, our results demonstrate genotoxic damage induced by goniothalamin in leukemic cells. Further studies are needed to ascertain the mode of action of goniothalamin in inducing DNA damage.