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首页> 外文期刊>Nutrition and Cancer: An International Journal >Role of Di-allyl disulfide, a garlic component in NF-κB mediated transient g2-m phase arrest and apoptosis in human leukemic cell-lines
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Role of Di-allyl disulfide, a garlic component in NF-κB mediated transient g2-m phase arrest and apoptosis in human leukemic cell-lines

机译:大蒜中的二烯丙基二硫化物在人白血病细胞系中由NF-κB介导的瞬时g2-m期阻滞和凋亡的作用

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Diallyl disulfide (DADS), the major organosulfur component of processed garlic is very effective in chemoprevention of several types of cancers; however, its detailed mechanism is yet to be divulged. Present study shows antiproliferative activity of DADS against human leukemic cell-lines, mainly U937. DADS induced transient G2/M phase arrest, which is evident from FACS analysis. The results revealed that a significant transcriptional induction of p21 happened in early hours of treatment, which is due to increased nuclear translocation of NF-κB and its specific binding to p21 promoter. However, in the later hours, G2/M arrest is lost leading to apoptosis via intrinsic mitochondria-mediated pathway through generation of reactive oxygen species followed by changes in mitochondrial membrane potential. Western blots indicate release of cytochrome-c, activation of caspase-3, cleavage of PARP1, and finally decrease in bcl-2 levels. In addition, inactivation of NF-κB by its inhibitor BAY 11-7085 causes early onset of apoptosis without any transient G2/M arrest. Thus, in conclusion, DADS induces reversible G2/M arrest through NF-κB mediated pathway in human leukemic cell lines, like U937, K562, and Jurkat, lacking wild type p53. However, G2/M arrest is lost owing to the incapability of the damage repair system that leads to apoptosis.
机译:二烯丙基二硫化物(DADS)是加工大蒜的主要有机硫成分,在化学预防多种癌症中非常有效。但是,它的详细机制还有待透露。目前的研究表明,DADS对人类白血病细胞系(主要是U937)具有抗增殖活性。 DADS诱导了短暂的G2 / M相停滞,这在FACS分析中很明显。结果表明,在治疗的早期,p21发生了明显的转录诱导,这是由于NF-κB的核易位增加及其与p21启动子的特异性结合所致。但是,在随后的几个小时中,G2 / M的阻滞作用丧失,从而通过内在的线粒体介导的途径导致细胞凋亡,该途径是通过产生活性氧,然后改变线粒体膜电位。蛋白质印迹表明细胞色素c的释放,caspase-3的激活,PARP1的裂解以及最终bcl-2水平的降低。此外,NF-κB抑制剂BAY 11-7085的失活导致细胞凋亡的早期发作,而没有任何短暂的G2 / M停滞。因此,结论是,DADS通过缺乏野生型p53的人白血病细胞系(如U937,K562和Jurkat)中的NF-κB介导的途径诱导了可逆的G2 / M阻滞。然而,由于损伤修复系统的能力不足导致细胞凋亡,G2 / M的阻滞作用丧失了。

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