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Map7/B2M的表达比率对II期结肠癌患者的生存具有预后价值。

The expression ratio of Map7/B2M is prognostic for survival in patients with stage II colon cancer.

作者信息

Blum Craig, Graham Amanda, Yousefzadeh Matt, Shrout Jessica, Benjamin Katie, Krishna Murli, Hoda Raza, Hoda Rana, Cole David J, Garrett-Mayer Elizabeth, Reed Carolyn, Wallace Michael, Mitas Michael

机构信息

Department of Surgery, Medical University of South Carolina, Charleston, SC 29425, USA.

出版信息

Int J Oncol. 2008 Sep;33(3):579-84.

Abstract

Colorectal cancer (CRC) is the second most frequent cause of cancer-related death in the United States. To determine whether certain molecular markers might be prognostic for survival, we measured by quantitative real-time RT-PCR the expression levels of 15 previously studied genes that are known to be up-regulated or down-regulated in the progression of epithelial cancers. The tumor samples were extracted from formalin-fixed paraffin-embedded primary tissues derived from patients with Stage II CRC who developed disease recurrence within two years (n=10), or were disease-free for at least 4 years (n=12). We were able to determine, by AUC curve analysis, that the ratio of microtubule associated protein 7 (Map7)/B2M was predictive of outcome in our sample set. Further, using Kaplan-Meier survival analysis, we observed significantly different curves as a function of marker positivity for the Map7/B2M (p=0.0001; HR=11) expression ratio. This suggests that the expression ratio of Map7/B2M may serve as a valuable prognostic marker in patients with Stage II colon cancer, and potentially guide therapeutic decision making.

摘要

结直肠癌(CRC)是美国癌症相关死亡的第二大常见原因。为了确定某些分子标记物是否可能对生存具有预后价值,我们通过定量实时逆转录聚合酶链反应(RT-PCR)测量了15个先前研究过的基因的表达水平,这些基因在上皮癌进展过程中已知会发生上调或下调。肿瘤样本取自福尔马林固定石蜡包埋的原发性组织,这些组织来自II期结直肠癌患者,其中10例在两年内出现疾病复发,12例至少4年无病。通过曲线下面积(AUC)分析,我们能够确定微管相关蛋白7(Map7)/β2微球蛋白(B2M)的比值可预测我们样本集的预后。此外,使用Kaplan-Meier生存分析,我们观察到Map7/B2M表达比值的标记物阳性状态与生存曲线存在显著差异(p=0.0001;风险比[HR]=11)。这表明Map7/B2M的表达比值可能是II期结肠癌患者有价值的预后标记物,并可能指导治疗决策。

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本文引用的文献

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CA Cancer J Clin. 2007 May-Jun;57(3):168-85. doi: 10.3322/canjclin.57.3.168.
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