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首页> 外文期刊>Immunology Letters >Effective inhibition of a Strongylocentrotus nudus eggs polysaccharide against hepatocellular carcinoma is mediated via immunoregulation in vivo.
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Effective inhibition of a Strongylocentrotus nudus eggs polysaccharide against hepatocellular carcinoma is mediated via immunoregulation in vivo.

机译:通过体内免疫调节介导对抗肝细胞癌的抗肝细胞癌的强血糖蛋白多糖的有效抑制。

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This study was aimed at evaluating the inhibitory effect of a polysaccharide that was isolated from Strongylocentrotus nudus eggs (SEP) against hepatocellular carcinoma in H22-bearing mice and elucidating its immunological mechanisms by determining its effects on the growth of transplanted tumors and immune response in H22-bearing mice. ICR mice inoculated with mouse hepatoma carcinoma cell lines H22 were treated with SEP at doses of 4, 8, 16 mg/kg/d for 12 days. The effects of SEP were measured via the growth of the transplanted tumors, splenocyte proliferation, T lymphocytes counts, CTL activity, the production of cytokines from splenocytes and the levels of serum Ig in tumor-bearing mice. In addition, the effects of SEP on Erk phosphorylation in mouse splenocytes and on the transcriptional activity of NFAT in Jurkat T cells were also investigated. Our results showed that SEP significantly inhibited the growth of transplanted tumors in mice. SEP could not only remarkably enhance splenocyte proliferation, CD4(+) and CD8(+) T cell numbers as well as CTL activity, but it also elevated IL-2 and TNF-alpha secretion as well as IgA, IgM and IgG levels in the serum. Furthermore, the activation of Erk phosphorylation and the NFAT promoter by SEP promoted the transcription and expression of downstream gene IL-2. In conclusion, our study demonstrates that SEP effectively inhibits hepatocellular carcinoma in vivo via enhancement of host immune system function, and it could be a potential therapeutic drug for hepatocarcinoma.
机译:本研究旨在评估多糖的抑制作用,该多糖从H22轴承小鼠中捕获肝细胞癌中的肝细胞癌,并通过确定其对H22中的移植肿瘤和免疫应答的生长来阐明其免疫机制 - 抱着老鼠。接种用小鼠肝癌癌细胞系H22的ICR小鼠用4,8,16mg / kg / d的剂量均匀处理12天。通过移植的肿瘤,脾细胞增殖,T淋巴细胞计数,CTL活性,来自脾细胞的细胞因子的产生和肿瘤轴承小鼠的血清Ig水平来测量SEP的影响。此外,还研究了SEP对小鼠脾细胞中ERK磷酸化和Jurkat T细胞NFAT转录活性的影响。我们的研究结果表明,SEP显着抑制了小鼠移植肿瘤的生长。 SEP不仅可以显着增强脾细胞增殖,CD4(+)和CD8(+)T细胞数以及CTL活性,但它也升高了IL-2和TNF-α分泌以及IgA,IgM和IgG水平血清。此外,SEP通过SEP激活ERK磷酸化和NFAT启动子促进了下游基因IL-2的转录和表达。总之,我们的研究表明,SEP通过增强宿主免疫系统功能有效抑制体内肝细胞癌,并且它可能是肝癌的潜在治疗药物。

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