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首页> 外文期刊>Surgery today >Role of interleukin-1alpha and type I interleukin-1 receptor in the growth activity and invasion of gastric carcinoma cells.
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Role of interleukin-1alpha and type I interleukin-1 receptor in the growth activity and invasion of gastric carcinoma cells.

机译:白细胞介素-1α和I型白介素-1受体在胃癌细胞生长和侵袭中的作用。

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摘要

To clarify the role of the interleukin (IL)-1/IL-1 receptor system in the progression of gastric carcinoma cells in patients with advanced gastric cancer, we measured the tissue concentrations of IL-1alpha, the expression of IL-1-receptor type I (IL-1RtI) on tumor cells, and the cell-growth activity through an analysis of DNA content. The concentrations of IL-1alpha were significantly higher in differentiated than in undifferentiated tumors (P = 0.038). The expression of IL-1RtI was upregulated in the tumor cells associated with INFgamma [corrected], scirrhous type tumors, and T3 and T4 tumors. There was a clear linear correlation between the tissue concentrations of IL-1alpha and S-phase fractions in differentiated tumors (r = 0.664, P = 0.003). Tumor cells with high IL-1alpha concentrations and low IL-1RtI expression had significantly greater S-phase fractions than those with low IL-1alpha concentrations, independent of IL-IRtI expression (P = 0.024 in low IL-1RtI, P = 0.019 in high IL-IRtI). These findings indicate that IL-1alpha stimulates the growth of differentiated gastric carcinoma cells and that IL-IRtI expression is involved in tumor invasive activity. High S-phase levels were not necessarily associated with a high expression of IL-1RtI, which may be due to the downregulatory effects of high IL-1alpha concentrations.
机译:为了阐明白细胞介素(IL)-1 / IL-1受体系统在晚期胃癌患者胃癌细胞进展中的作用,我们测量了IL-1α的组织浓度,IL-1受体的表达肿瘤细胞上的I型(IL-1RtI),以及通过分析DNA含量的细胞生长活性。分化中的IL-1α浓度明显高于未分化的肿瘤(P = 0.038)。 IL-1RtI的表达在与INFgamma(校正),硬化型肿瘤以及T3和T4肿瘤相关的肿瘤细胞中上调。在分化的肿瘤中,IL-1α的组织浓度与S期组分之间存在明显的线性相关性(r = 0.664,P = 0.003)。高IL-1alpha浓度和低IL-1RtI表达的肿瘤细胞的S期分数比低IL-1alpha浓度高得多,独立于IL-IRtI表达(低IL-1RtI的P = 0.024,低IL-1RtI的P = 0.019)。高IL-IRtI)。这些发现表明IL-1α刺激分化的胃癌细胞的生长,并且IL-IRtI表达与肿瘤侵袭活性有关。高S期水平不一定与IL-1RtI的高表达有关,这可能是由于高IL-1alpha浓度的下调作用所致。

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