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Molecular Mechanisms Underlying the Inhibitory Effects of Qingzaojiufei Decoction on Tumor Growth in Lewis Lung Carcinoma

机译:清早九飞汤抑制刘易斯肺癌肿瘤生长的分子机制

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Objective: Qingzaojiufei decoction (QD) is an empirical herbal formula from traditional Chinese medicine that is used for the treatment of lung-related diseases. However, the effect of QD on the growth of lung tumor cells has not been investigated. The aim of this study was to examine the antitumor activity of QD in Lewis lung carcinomas (LLC) in vivo and in vitro, and to elucidate the underlying mechanisms. Methods: The LLC cells were used to assess the antitumor activity of QD by Cell Counting Kit-8 assay in vitro. In vivo, mice were randomly assigned to 5 groups (n = 10/group): the model control (MC) group was intragastrically administered physiological saline (0.9% NaCl) twice daily from day 2 after tumor implantation for 2 weeks. The QD groups were intragastrically administered QD twice daily from 2 weeks before to 2 weeks after tumor implantation for 4 weeks. The mRNA levels were detected by quantitative polymerase chain reaction, the proteins expression was determined by immunohistochemistry or western blotting. Results: Compared with the model group, QD showed inhibition of proliferation of LLC cells and reductions in tumor weight and proliferating cell nuclear antigen protein expression. Furthermore, QD up-regulated p53 mRNA expression, and downregulated c-myc and Bcl-2 mRNA expression, while MMP-9, VEGF, and VEGFR protein expression was suppressed. Phosphorylated ERK1/2 levels were also reduced by QD in a dose-dependent manner. Conclusion: Our findings suggest that QD inhibited lung tumor growth and proliferation, by activation of tumor suppressor genes, inactivation of oncogenes, suppressing the potential for invasion and metastasis, and attenuating angiogenesis. The ERK/VEGF/MMPs signaling pathways may play an important role in QD-induced inhibition of malignant tumor cell proliferation.
机译:目的:青枣九飞汤(QD)是一种中药治疗肺部疾病的经验性中药配方。但是,尚未研究QD对肺肿瘤细胞生长的影响。这项研究的目的是检查体内和体外QD在Lewis肺癌(LLC)中的抗肿瘤活性,并阐明其潜在机制。方法:通过细胞计数试剂盒8(Cell Counting Kit-8)体外检测LLC细胞的QD抗肿瘤活性。在体内,将小鼠随机分为5组(n = 10 /组):从肿瘤植入2周后的第二天起,每天两次向模型对照组(MC)胃内注射生理盐水(0.9%NaCl)。从肿瘤植入前2周至植入后2周,每天两次QD组在胃内进行QD,持续4周。通过定量聚合酶链反应检测mRNA水平,通过免疫组织化学或蛋白质印迹确定蛋白质表达。结果:与模型组相比,量子点显示出抑制LLC细胞的增殖,降低肿瘤重量和增殖细胞核抗原蛋白的表达。此外,QD上调p53 mRNA表达,下调c-myc和Bcl-2 mRNA表达,而MMP-9,VEGF和VEGFR蛋白表达受到抑制。 QD还以剂量依赖的方式降低了磷酸化的ERK1 / 2水平。结论:我们的发现表明,量子点可通过激活抑癌基因,灭活癌基因,抑制侵袭和转移的潜能以及减弱血管生成来抑制肺肿瘤的生长和增殖。 ERK / VEGF / MMPs信号通路可能在QD诱导的恶性肿瘤细胞增殖抑制中起重要作用。

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