...
首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Rice Bran Phytic Acid Induced Apoptosis Through Regulation of Bcl-2/Bax and p53 Genes in HepG2 Human Hepatocellular Carcinoma Cells
【24h】

Rice Bran Phytic Acid Induced Apoptosis Through Regulation of Bcl-2/Bax and p53 Genes in HepG2 Human Hepatocellular Carcinoma Cells

机译:米糠植物诱导通过调节HepG2人肝细胞癌细胞的Bcl-2 / Bax和P53基因的细胞凋亡

获取原文
           

摘要

Phytic acid (PA) has been reported to have positive nutritional benefits and prevent cancer formation. This study investigated the anticancer activity of rice bran PA against hepatocellular carcinoma (HepG2) cells. Cytotoxicty of PA (0.5 to 4mM) was examined by MTT and LDH assays after 24 and 48h treatment. Apoptotic activity was evaluated by expression analysis of apoptosis-regulatory genes [i.e. p53, Bcl-2, Bax, Caspase-3 and -9] by reverse transcriptase-PCR and DNA fragmentation assay. The results showed antioxidant activity of PA in Fe3+ reducing power assay ( ). PA inhibited the growth of HepG2 cells in a concentration dependent manner ( ). After 48h treatment, cell viability was recorded 84.7, 74.4, 65.6, 49.6, 36.0 and 23.8% in MTT assay and 92.6, 77.0%, 66.8%, 51.2, 40.3 and 32.3% in LDH assay at concentrations of 1, 1.5, 2.0, 2.5, 3.0, and 3.5mM, respectively. Hence, treatment of PA for 24h, recorded viability of cells 93.5, 88.6, 55.5, 34.6 and 24.4% in MTT assay and 94.2, 86.1%, 59.7%, 42.3 and 31.6%, in LDH assay at concentrations of 1, 2.2, 3.0, 3.6 and 4.0mM, respectively. PA treated HepG2 cells showed up-regulation of p53, Bax, Caspase-3 and -9, and down-regulation of Bcl-2 gene ( ). At the (2.49mM) of PA, the p53, Bax, Caspase-3 and-9 genes were up-regulated by 6.03, 7.37, 19.7 and 14.5 fold respectively. Also, the fragmented genomic DNA in PA treated cells provided evidence of apoptosis. Our study confirmed the biological activity of PA and demonstrated growth inhibition and induction of apoptosis in HepG2 cells with modulation of the expression of apoptosis-regulatory genes.
机译:据报道,植物酸(PA)具有阳性营养益处并预防癌症形成。本研究研究了米糠PA对肝细胞癌(HepG2)细胞的抗癌活性。通过24至48h处理后MTT和LDH测定检查PA(0.5至4mm)的细胞毒素。通过表达分析凋亡调节基因的表达分析评价凋亡活性[即通过逆转录酶-PCR和DNA碎片测定,P53,BCL-2,BAX,Caspase-3和-9]。结果显示了Fe3 +降低功率测定()中PA的抗氧化活性。 PA抑制浓度依赖性方式()的HepG2细胞的生长。在48h处理后,在MTT测定中记录细胞活力84.7,74.4,65.6,49.6,36.0和23.8%,在1,1.5,2.0的浓度下,LDH测定中的92.6,77.0%,66.8%,51.2,40.3和32.3%。 2.5,3.0和3.5mm。因此,在LDH测定中,在MTT测定中,在MTT测定中的浓度为1,20,3.0的LDH测定中,将PA的PA持续24h,记录的细胞93.5,85.6,55.5,55.5,31,34.6和24.4%,42.3和31.6%。分别为3.6和4.0mm。 PA处理的HepG2细胞显示P53,Bax,Caspase-3和-9的上调,以及Bcl-2基因()的下调。在Pa的(2.49mm),P53,Bax,Caspase-3和-9基因分别上调6.03,7.37,19.7和14.5倍。此外,PA处理细胞中的碎片基因组DNA提供了凋亡的证据。我们的研究证实了PA的生物活性,并显示了HepG2细胞中凋亡的生长抑制和诱导,并调节了凋亡调节基因的表达。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号