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丹皮酚通过诱导肿瘤细胞凋亡以及刺激白细胞介素-2和肿瘤坏死因子-α的产生,对荷HepA肝癌小鼠模型产生抗肿瘤作用。

Anti-tumor effects of paeonol in a HepA-hepatoma bearing mouse model via induction of tumor cell apoptosis and stimulation of IL-2 and TNF-alpha production.

作者信息

Sun Guo-Ping, Wang Hua, Xu Shu-Ping, Shen Yu-Xian, Wu Qiang, Chen Zhen-Dong, Wei Wei

机构信息

Department of Oncology, The First Affiliated Hospital of Anhui Medical University; Hefei, 230032, China.

出版信息

Eur J Pharmacol. 2008 Apr 28;584(2-3):246-52. doi: 10.1016/j.ejphar.2008.02.016. Epub 2008 Feb 15.

Abstract

Paeonol, a phenolic component from the root bark of Paeonia moutan, is traditionally used as a Chinese herbal medicine to activate the blood flow and remove blood stasis. Evidence shows that paeonol have anti-tumor, anti-inflammatory, and analgesic effects; however, the underlying mechanisms remain unknown. In this study, we investigated the molecular mechanisms by which paeonol exerts the anti-tumor effects by using a murine model of hepatoma established by in vivo injection of mouse HepA-hepatoma cells. Treatment of mice with 100, 200, or 400 mg/kg/day of paeonol significantly inhibited the growth of the HepA tumor in mice, induced HepA cell apoptosis as demonstrated by light microscopy and electron microscopy analyses, decreased the expression of Bcl-2 and increased the expression of Bax in HepA tumor tissues in a dose-related manner. Administration of paeonol in vivo also elevated serum levels of IL-2 and TNF-alpha in tumor-bearing mice. Moreover, splenocytes and macrophages isolated from paeonol-treated HepA tumor-bearing mice produced higher levels of IL-2 and TNF-alpha in response to concanavalin A and lipopolysaccharide stimulation, respectively, compared to these isolated from non-treated HepA tumor-bearing mice. In vitro treatment with paeonol was able to directly stimulate IL-2 and TNF-alpha production in splenocytes and macrophages from tumor-bearing mice, respectively. In conclusion, paeonol has the anti-tumor effect against hepatoma cells, which are likely mediated via induction of tumor cell apoptosis and stimulation of IL-2 and TNF-alpha production. Paeonol could be a promising drug to treat hepatocellular carcinoma.

摘要

丹皮酚是牡丹根皮中的一种酚类成分,传统上用作活血化瘀的中药材。有证据表明,丹皮酚具有抗肿瘤、抗炎和镇痛作用;然而,其潜在机制尚不清楚。在本研究中,我们通过体内注射小鼠HepA肝癌细胞建立的肝癌小鼠模型,研究了丹皮酚发挥抗肿瘤作用的分子机制。用100、200或400mg/kg/天的丹皮酚治疗小鼠,显著抑制了小鼠体内HepA肿瘤的生长,光镜和电镜分析表明诱导了HepA细胞凋亡,以剂量相关的方式降低了HepA肿瘤组织中Bcl-2的表达并增加了Bax的表达。丹皮酚体内给药还提高了荷瘤小鼠血清IL-2和TNF-α水平。此外,与未处理的荷HepA肿瘤小鼠分离的脾细胞和巨噬细胞相比,从经丹皮酚处理的荷HepA肿瘤小鼠分离的脾细胞和巨噬细胞分别对伴刀豆球蛋白A和脂多糖刺激产生更高水平的IL-2和TNF-α。体外丹皮酚处理能够分别直接刺激荷瘤小鼠脾细胞和巨噬细胞产生IL-2和TNF-α。总之,丹皮酚对肝癌细胞具有抗肿瘤作用,这可能是通过诱导肿瘤细胞凋亡以及刺激IL-2和TNF-α产生来介导的。丹皮酚可能是一种有前途的治疗肝细胞癌的药物。

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