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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Macrophage inhibitory cytokine 1: a new prognostic marker in prostate cancer.
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Macrophage inhibitory cytokine 1: a new prognostic marker in prostate cancer.

机译:巨噬细胞抑制性细胞因子1:前列腺癌的新预后标志物。

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摘要

PURPOSE: High serum levels of macrophage inhibitory cytokine 1 (MIC-1) are strongly associated with metastatic prostate cancer, suggesting MIC-1 is a biomarker for prostate cancer prognosis. EXPERIMENTAL DESIGN: We conducted a prospective cohort study of 1,442 Swedish men with a pathologically verified diagnosis of prostate cancer between 2001 and 2003. Blood was drawn either pretreatment (n = 431) or posttreatment (n = 1,011) and cases were followed for a mean time of 4.9 years (range, 0.1-6.8 years). RESULTS: MIC-1 serum levels independently predicted poor cancer-specific survival with an almost 3-fold higher cancer death rate in patients with serum levels in the highest quartile compared with men with serum levels in the lowest quartile (adjusted hazard ratio, 2.98; 95% confidence interval, 1.82-4.68). Pretreatment MIC-1 levels revealed an even stronger association with disease outcome with an 8-fold higher death rate in the highest compared with the lowest category (adjusted hazard ratio, 7.98; 95% confidence interval, 1.73-36.86). Among patients considered to have localized disease, MIC-1 significantly increased the discriminative capacity between indolent and lethal prostate cancer compared with the established prognostic markers clinical stage, pathologic grade, and prostate-specific antigen level (P = 0.016). A sequence variant in the MIC-1 gene was associated with decreased MIC-1 serum levels (P = 0.002) and decreased prostate cancer mortality (P = 0.003), suggesting a causative role of MIC-1 in prostate cancer prognosis. CONCLUSIONS: Serum MIC-1 concentration is a novel biomarker capable of predicting prostate cancer prognosis.
机译:目的:血清高水平的巨噬细胞抑制细胞因子1(MIC-1)与转移性前列腺癌密切相关,表明MIC-1是前列腺癌预后的生物标志物。实验设计:我们进行了一项前瞻性队列研究,研究对象为2001年至2003年经病理检查证实为前列腺癌的1,442名瑞典男性。在治疗前(n = 431)或治疗后(n = 1,011)抽取血液,并对病例进行平均随访时间为4.9年(范围为0.1-6.8年)。结果:MIC-1血清水平独立预测较差的癌症患者的特异性癌症存活率,最高四分位数血清患者的癌症死亡率几乎是最低四分位数男性的癌症死亡率的三倍(调整后的危险比为2.98; 95%置信区间1.82-4.68)。预处理MIC-1水平显示与疾病结局的关联更强,最高死亡率比最低疾病类别高8倍(调整后的危险比为7.98; 95%的置信区间为1.73-36.86)。在已确定的局部疾病患者中,与已建立的预后标志物临床阶段,病理分级和前列腺特异性抗原水平相比,MIC-1显着提高了惰性和致死性前列腺癌的鉴别能力(P = 0.016)。 MIC-1基因的序列变异与MIC-1血清水平降低(P = 0.002)和前列腺癌死亡率降低(P = 0.003)相关,表明MIC-1在前列腺癌预后中起着重要作用。结论:血清MIC-1浓度是一种能够预测前列腺癌预后的新型生物标志物。

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