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灵芝多糖对B16F10细胞中转化生长因子β1、白细胞介素-10和血管内皮生长因子产生的抑制作用。

Suppression of the production of transforming growth factor β1, interleukin-10, and vascular endothelial growth factor in the B16F10 cells by Ganoderma lucidum polysaccharides.

作者信息

Sun Li-Xin, Lin Zhi-Bin, Duan Xin-Suo, Qi Hai-Hua, Yang Ning, Li Min, Xing En-Hong, Sun Yu, Yu Min, Li Wei-Dong, Lu Jie

机构信息

1 The Affiliated Hospital of Chengde Medical College , Chengde, Hebei Province, China .

出版信息

J Interferon Cytokine Res. 2014 Sep;34(9):667-75. doi: 10.1089/jir.2012.0101. Epub 2014 Mar 27.

Abstract

Transforming growth factor β (TGF-β), interleukin-10 (IL-10), and vascular endothelial growth factor (VEGF) are three of the commonly studied cytokines playing an important role in tumor initiation and progression. Besides their promotional effects on tumor progression, the three cytokines have immunosuppressive effects that facilitate tumor initiation and progression as well. Ganoderma lucidum polysaccharides (Gl-PS) with multiple bioactivities may have the effect on B16F10 melanoma cells to induce stronger antitumor immune response that has been demonstrated. Gl-PS may have the suppressive effects on the production of these three cytokines, which has yet to be demonstrated. In this study, we tested these effects of Gl-PS by incubating Gl-PS with malignant tumor cells such as B16F10 cells, a melanoma cell line, and LA795 cells, a lung carcinoma cell line. RT-qPCR and enzyme-linked immunosorbent assay showed that the production of TGF-β1, IL-10, and VEGF in B16F10 melanoma cells and LA795 lung carcinoma cells was suppressed by Gl-PS at both mRNA and protein levels, suggesting that the suppression on production of TGF-β, IL-10, and VEGF in B16F10 melanoma cells and LA795 lung carcinoma cells by Gl-PS may contribute to the therapy on melanoma and lung carcinoma along with the induction of stronger antitumor immune response.

摘要

转化生长因子β(TGF-β)、白细胞介素-10(IL-10)和血管内皮生长因子(VEGF)是三种常见的细胞因子,在肿瘤的发生和发展中发挥着重要作用。除了对肿瘤进展有促进作用外,这三种细胞因子还具有免疫抑制作用,也有助于肿瘤的发生和发展。具有多种生物活性的灵芝多糖(Gl-PS)可能对B16F10黑色素瘤细胞有作用,可诱导更强的抗肿瘤免疫反应,这一点已得到证实。Gl-PS可能对这三种细胞因子的产生有抑制作用,但尚未得到证实。在本研究中,我们通过将Gl-PS与恶性肿瘤细胞(如黑色素瘤细胞系B16F10细胞和肺癌细胞系LA795细胞)孵育来测试Gl-PS的这些作用。逆转录定量聚合酶链反应(RT-qPCR)和酶联免疫吸附测定表明,Gl-PS在mRNA和蛋白质水平上均抑制了B16F10黑色素瘤细胞和LA795肺癌细胞中TGF-β1、IL-10和VEGF的产生,这表明Gl-PS对B16F10黑色素瘤细胞和LA795肺癌细胞中TGF-β、IL-10和VEGF产生的抑制作用可能有助于黑色素瘤和肺癌的治疗,同时诱导更强的抗肿瘤免疫反应。

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