Zhou W, Sokoll L J, Bruzek D J, Zhang L, Velculescu V E, Goldin S B, Hruban R H, Kern S E, Hamilton S R, Chan D W, Vogelstein B, Kinzler K W
Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.
Cancer Epidemiol Biomarkers Prev. 1998 Feb;7(2):109-12.
To begin to identify new tumor markers, we recently performed a systematic study of gene expression in cancers of the colon and pancreas. Of the 45,000 genes identified, 183 were found to be expressed at significantly elevated levels in pancreatic cancer. One of the genes was tissue inhibitor of metalloproteinase type I (TIMP-1), which encodes a secreted protein. Analysis of TIMP-1 serum levels revealed significant increases in pancreatic cancer patients, but TIMP-1 by itself was inadequate as a serum marker for cancer. However, a combination of individually suboptimal markers (TIMP-1, CA19-9, and carcinoembryonic antigen) detected 60% of 85 patients with pancreatic cancers in a highly specific manner. These results suggest that a systematic analysis of gene expression can reveal novel serum markers and that individually suboptimal markers can be combined to yield higher sensitivity and specificity.
为了开始鉴定新的肿瘤标志物,我们最近对结肠癌和胰腺癌的基因表达进行了一项系统性研究。在鉴定出的45000个基因中,发现有183个在胰腺癌中表达水平显著升高。其中一个基因是I型金属蛋白酶组织抑制剂(TIMP-1),它编码一种分泌蛋白。对TIMP-1血清水平的分析显示,胰腺癌患者的TIMP-1血清水平显著升高,但TIMP-1自身作为癌症血清标志物并不充分。然而,将各自不太理想的标志物(TIMP-1、CA19-9和癌胚抗原)组合起来,以高度特异性的方式检测出了85例胰腺癌患者中的60%。这些结果表明,对基因表达进行系统性分析可以揭示新的血清标志物,并且可以将各自不太理想的标志物组合起来以获得更高的敏感性和特异性。