Ganoderma lucidum polysaccharide extract inhibits hepatocellular carcinoma growth by downregulating regulatory T cells accumulation and function by inducing microRNA-125b

被引:98
|
作者
Li, Aimei [1 ,2 ]
Shuai, Xuanyu [1 ]
Jia, Zhijun [2 ]
Li, Hangyu [3 ]
Liang, Xiubin [5 ]
Su, Dongming [1 ,4 ,5 ]
Guo, Wanhua [2 ]
机构
[1] Nanjing Med Univ, Dept Pathol, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, Drum Tower Hosp, Dept Nucl Med, Nanjing 210008, Jiangsu, Peoples R China
[3] China Med Univ, Shengjing Hosp, Dept Gen Surg, Shenyang 110001, Peoples R China
[4] Nanjing Med Univ, Affiliated Hosp 2, Ctr Cellular Therapy, Nanjing, Jiangsu, Peoples R China
[5] Nanjing Med Univ, Ctr Metab Dis Res, Nanjing 210029, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Ganoderma lucidum polysaccharides; Hepatocellular carcinoma; Regulatory T cell; Effector T cell; miR-125b; IN-VITRO; CANCER; EXPRESSION; ANTITUMOR; MICE; IMMUNITY; NOTCH1; VIVO;
D O I
10.1186/s12967-015-0465-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Ganoderma lucidum polysaccharides (GLPS) have been used as traditional Chinese medicine for their properties of cancer prevention and immunomodulation. However, it is unclear whether GLPS has therapeutic effect on anti-hepatocellular carcinoma (HCC) in vivo. In this study, the effect of GLPS and their impact on the balance of regulatory T cell (Treg) and effector T cell (Teff) was measured in a model of hepatoma-bearing mice. Methods: The effect of GLPS and their impact on the balance of regulatory T cell (Treg) and effector T cell (Teff) were measured in a model of hepatoma-bearing mice. Real-time PCR detected the levels of MicroRNAs (miRNAs) and mRNA. The effects of Tregs on Teff proliferation were determined via suppression assay. The mircroRNA-125b (miR-125b) inhibitor was used to down-regulate miR-125b expression. Results: GLPS significantly suppressed tumor growth in hepatoma-bearing mice associated with an increase of the ratio of Teffs to Tregs. Moreover, GLPS eliminate Treg suppression of Teff proliferation with an increase in IL-2 secretion. Addition of GLPS to treat T cells inhibited Notch1 and FoxP3 expression through increase of miR-125b expression. In hepatoma-bearing mice, miR-125b inhibitor obviously abolished the effect of GLPS on tumor growth. Conclusions: This finding provides the novel evidence for GLPS on inhibition of HCC through miR-125b inhibiting Tregs accumulation and function.
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页数:10
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