Kumar Sanjay, Tomar Munendra Singh, Acharya Arbind
Centre of Advance Study in Zoology, Faculty of Science, Banaras Hindu University , Varanasi , India.
Leuk Lymphoma. 2015 Jun;56(6):1846-55. doi: 10.3109/10428194.2014.974042. Epub 2015 Jan 8.
The p53 tumor suppressor protein has been implicated as an activator of apoptosis. In order to investigate the effect of chelerythrine and staurosporine on the activation of p53-dependent/-independent pathways of Dalton lymphoma (DL) cell death, cells were treated with chelerythrine and staurosporine for 1 h, 3 h and 6 h, respectively. It was found that treatment with chelerythrine and staurosporine increased the expression of total-p53/phospho-53 (ser-15) significantly at protein and mRNA levels, which resulted in activation of the p53-dependent apoptotic pathway in DL cells. In addition, increased activities of cyt-c, caspase-9 and caspase-3 and degradation of DNA into fragments confirmed activation of the p53-independent apoptotic pathway in p53 knockdown RNAi-DL cells. In brief, the present study demonstrated activation of p53-dependent/-independent apoptotic pathways in DL cells. Therefore, targeting of p53-dependent/-independent apoptotic pathways may lead to the possibility of designing and developing better therapeutic regimens to treat DL and other human cancers.
p53肿瘤抑制蛋白被认为是细胞凋亡的激活剂。为了研究白屈菜红碱和星形孢菌素对道尔顿淋巴瘤(DL)细胞死亡的p53依赖性/非依赖性途径激活的影响,分别用白屈菜红碱和星形孢菌素处理细胞1小时、3小时和6小时。结果发现,用白屈菜红碱和星形孢菌素处理后,总p53/磷酸化p53(丝氨酸15)在蛋白质和mRNA水平上的表达显著增加,这导致DL细胞中p53依赖性凋亡途径的激活。此外,细胞色素c、半胱天冬酶-9和半胱天冬酶-3活性的增加以及DNA降解成片段证实了p53基因敲低的RNAi-DL细胞中p53非依赖性凋亡途径的激活。简而言之,本研究证明了DL细胞中p53依赖性/非依赖性凋亡途径的激活。因此,针对p53依赖性/非依赖性凋亡途径可能会带来设计和开发更好的治疗方案来治疗DL和其他人类癌症的可能性。