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Evaluating macrophage migration inhibitory factor 1 expression as a prognostic biomarker in colon cancer

机译:评估巨噬细胞迁移抑制因子1表达作为结肠癌的预后生物标志物

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Objective: Several studies indicate that macrophage migration inhibitory factor 1 plays a role for tumor progression in colon cancer. We investigated whether determination of migration inhibitory factor 1 mRNA expression levels in lymph nodes of colon cancer patients could be used as a prognostic marker. Methods: Expression levels of migration inhibitory factor 1 and carcinoembryonic antigen mRNAs were assessed in primary tumors and regional lymph nodes of 123 colon cancer patients (stages I–IV), and in colon cancer- and immune cell lines using quantitative reverse transcriptase–polymerase chain reaction. Expression of migration inhibitory factor 1 protein was investigated by two-color immunohistochemistry and immunomorphometry. Results: Migration inhibitory factor 1 mRNA was expressed at 60 times higher levels in primary colon cancer tumors compared to normal colonic tissue (medians 8.2 and 0.2 mRNA copies/18S rRNA unit; p??.0001). A highly significant difference in mRNA expression levels was found between hematoxylin-eosin positive lymph nodes and hematoxylin-eosin negative lymph nodes (p??.0001). Migration inhibitory factor 1 and carcinoembryonic antigen proteins were simultaneously expressed in many colon cancer-tumor cells. Kaplan–Meier survival model and hazard ratio analysis, using a cutoff level at 2.19 mRNA copies/18S rRNA unit, revealed that patients with lymph nodes expressing high levels of migration inhibitory factor 1 mRNA had a 3.5-fold (p?=?.04) higher risk for recurrence, associated with a small, but significant, difference in mean survival time (7?months, p?=?.03) at 12?years of follow-up. Conclusion: Although migration inhibitory factor 1 mRNA expression levels were related to severity of disease and lymph node analysis revealed that colon cancer patients with high levels had a shorter survival time after surgery than those with low levels, the difference was small and probably not useful in clinical practice.
机译:目的:几项研究表明,巨噬细胞迁移抑制因子1在结肠癌中发挥肿瘤进展的作用。我们研究了结肠癌患者的淋巴结中迁移抑制因子1 mRNA表达水平的测定是否可以用作预后标志物。方法:在123例结肠癌患者(阶段I-IV)的原发性肿瘤和区域淋巴结和区域淋巴结和使用定量逆转录酶 - 聚合酶链中,评估迁移抑制因子1和癌胚胎抗原MRNA的表达水平,以及结肠癌和免疫细胞系反应。用双色免疫组织化学和免疫形状研究了迁移抑制因子1蛋白的表达。结果:与正常结肠组织(中位数8.2和0.2 mRNA拷贝/ 18s rRNA单位)相比,迁移抑制因子1mRNA在原子结肠癌肿瘤中的60倍以下的较高水平。p?<0001)。在苏木精 - 嗜素阳性淋巴结和苏木精 - 曙红阴性淋巴结之间发现mRNA表达水平的高度显着差异(p≤10001)。在许多结肠癌肿瘤细胞中同时表达迁移抑制因子1和癌胚抗原蛋白。 Kaplan-Meier生存模型和危险比分析,在2.19 mRNA拷贝/ 18s rRNA单位的情况下,表达表达高水平迁移抑制因子1 mRNA的淋巴结患者具有3.5倍(p?=Δ.04 )复发的危险程度较高,与小而且显着,平均存活时间差异(7?月,P?=Δ.03)在12年后续行动的情况下。结论:虽然迁移抑制因子1 mRNA表达水平与疾病的严重程度有关,但淋巴结分析显示,患有高水平的结肠癌患者在手术后的存活时间较短,差异很小,可能没有用临床实践。

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