首页> 外文期刊>BioMed research international >Trigonella foenum (Fenugreek) Induced Apoptosis in Hepatocellular Carcinoma Cell Line, HepG2, Mediated by Upregulation of p53 and Proliferating Cell Nuclear Antigen
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Trigonella foenum (Fenugreek) Induced Apoptosis in Hepatocellular Carcinoma Cell Line, HepG2, Mediated by Upregulation of p53 and Proliferating Cell Nuclear Antigen

机译:Trigonella foenum(Fenugreek)诱导肝细胞癌细胞系细胞凋亡,Hepg2,由P53的上调介导和增殖细胞核抗原介导

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Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide and most current therapies are of limited efficacy. Trigonella foenum {Fenugreek) is a traditional herbal plant with antitumor activity, although the mechanisms of its activity remain unclear. Herein, a crude methanol extract was prepared from Fenugreek seeds (FCE) and its anticancer mechanism was evaluated, using HepG2 cell line. Growth-inhibitory effect and apoptosis induction of HepG2 cells were evidenced by MTT assay, cell morphology alteration, apoptosis enzyme-linked immunosorbent assay, flow cytometric analysis, caspase-3 activity, and expression of p53, proapoptotic protein, Bax, and proliferating cell nuclear antigen (PCNA) after (100~500 μg/mL) FCE treatment for 48 h. Furthermore, FCE was analyzed by Chromatography-Mass Spectrometry (GC/MS). Our results revealed that FCE treatment for 48 h showed a cytotoxic effect and apoptosis induction in a dose-dependent manner that was mediated by upregulation of p53, Bax, PCNA, and caspase-3 activation in HepG2 cells. GC-MS analysis of FCE showed the presence of fourteen bioactive compounds such as Terpenoids and Flavonoids, including two main constituents with anticancer activity, Squalene and Naringenin (27.71% and 24.05%), respectively. Our data introduced FCE as a promising nontoxic herbal with therapeutic potential to induce apoptosis in HepG2 cells through p53, Bax, and PCNA upregulation in caspase-3 dependent manner.
机译:肝细胞癌(HCC)是全球最常见的癌症之一,大多数当前疗法有限。 Trigonella foenum {Fenugreek)是一种传统的草药植物,但其活动的机制仍然不清楚。这里,使用HepG2细胞系评估粗甲醇提取物,并评估其抗癌机制。 MTT测定,细胞形态学改变,细胞凋亡酶联免疫吸附测定,流式细胞术分析,Caspase-3活性和P53,Proapoottic蛋白,Bax和增殖细胞核的表达证明了HepG2细胞的生长抑制作用和凋亡诱导抗原(PCNA)(100〜500μg/ ml)FCE治疗48小时。此外,通过色谱 - 质谱(GC / MS)分析FCE。我们的研究结果表明,48小时的FCE治疗显示了一种细胞毒性效应和以剂量依赖性方式诱导,所述剂量依赖性方式通过在HepG2细胞中的p53,Bax,PCNA和Caspase-3活化的上调介导。 FCE的GC-MS分析显示出存在十四种生物活性化合物,如三萜类化合物和黄酮类化合物,包括分别具有抗癌活性的两个主要成分,Squalene和Naringenin(27.71%和24.05%)。我们的数据引入了FCE作为具有治疗潜力的有前途的无毒性草药,其通过P53,BAX和PCNA上调在Caspase-3依赖性方式中诱导HepG2细胞的细胞凋亡。

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