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虎杖总黄酮的化学成分及其对肝癌细胞的促凋亡作用:抑制STAT3信号通路的潜在作用

Chemical composition of total flavonoids from Polygonum amplexicaule and their pro-apoptotic effect on hepatocellular carcinoma cells: Potential roles of suppressing STAT3 signaling.

作者信息

Xiang Meixian, Su Hanwen, Hong Zongguo, Yang Tianming, Shu Guangwen

机构信息

College of Pharmacy, South-Central University for Nationalities, Wuhan, China.

Renmin Hospital, Wuhan University, Wuhan, China.

出版信息

Food Chem Toxicol. 2015 Jun;80:62-71. doi: 10.1016/j.fct.2015.02.020. Epub 2015 Mar 6.

Abstract

Polygonum amplexicaule D. Don var. sinense Forb (P. amplexicaule) is a medical plant traditionally used in the treatment of malignant diseases including hepatocellular carcinoma (HCC), but the scientific basis underlying its anti-HCC activity remains poorly understood. Here, we explored the chemical profile of total flavonoids from P. amplexicaule (TFPA). Nine compounds that constituted the major components of TFPA were separated and identified. Further investigations revealed that TFPA dose-dependently induced HepG2, Huh-7 and H22 HCC cell apoptosis. In HCC cells, TFPA dramatically inhibited the transcriptional activity of signal transducer and activator of transcription 3 (STAT3). In addition, TFPA increased the expression of SHP-1, a protein tyrosine phosphatase catalyzing STAT3 dephosphorylation, in HCC cells. Animal studies showed that TFPA considerably provoked transplanted H22 cell apoptosis with undetectable toxicological effects on tumor-bearing mice. Consistently, TFPA dose-dependently inhibited transcriptional activity of STAT3 in transplanted tumor tissues. This study collectively demonstrated that TFPA has the capacity of inducing HCC cell apoptosis both in vitro and in vivo with low toxic effects on normal hepatocytes and vital organs of tumor-bearing mice. Suppressing STAT3 signaling is implicated in TFPA-mediated HCC cell apoptosis.

摘要

抱茎蓼(Polygonum amplexicaule D. Don var. sinense Forb)是一种传统上用于治疗包括肝细胞癌(HCC)在内的恶性疾病的药用植物,但其抗HCC活性的科学依据仍知之甚少。在此,我们探究了抱茎蓼总黄酮(TFPA)的化学特征。分离并鉴定了构成TFPA主要成分的9种化合物。进一步研究表明,TFPA能剂量依赖性地诱导HepG2、Huh-7和H22 HCC细胞凋亡。在HCC细胞中,TFPA显著抑制信号转导和转录激活因子3(STAT3)的转录活性。此外,TFPA增加了HCC细胞中SHP-1的表达,SHP-1是一种催化STAT3去磷酸化的蛋白酪氨酸磷酸酶。动物研究表明,TFPA能显著诱导移植的H22细胞凋亡,且对荷瘤小鼠无明显毒理学影响。同样,TFPA能剂量依赖性地抑制移植瘤组织中STAT3的转录活性。本研究共同表明,TFPA具有在体外和体内诱导HCC细胞凋亡的能力,且对正常肝细胞和荷瘤小鼠的重要器官毒性作用低。抑制STAT3信号传导与TFPA介导的HCC细胞凋亡有关。

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