Watanabe Toshiaki, Kobunai Takashi, Toda Etsuko, Kanazawa Takamitsu, Kazama Yoshihiro, Tanaka Junichiro, Tanaka Toshiaki, Yamamoto Yoko, Hata Keisuke, Kojima Tetsu, Yokoyama Tadashi, Konishi Tsuyoshi, Okayama Yoshihiro, Sugimoto Yoshikazu, Oka Toshinori, Sasaki Shin, Ajioka Yohichi, Muto Tetsuichiro, Nagawa Hirokazu
Department of Surgery, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.
Clin Cancer Res. 2007 Jan 15;13(2 Pt 1):415-20. doi: 10.1158/1078-0432.CCR-06-0753.
Ulcerative colitis (UC) is associated with a high risk of colorectal cancer. To identify genes that could predict the development of cancer in UC, we conducted a DNA microarray analysis using nonneoplastic rectal mucosa of UC patients.
Gene expression in nonneoplastic mucosa of 53 UC patients were examined. Gene expression profiles were examined using human Genome U133 Plus 2.0 gene chip array (Affymetrix). Among 53 UC patients, 10 had UC-associated cancer (UC-Ca group) whereas 43 did not (UC-NonCa group).
By comparing gene expression profiles of nonneoplastic rectal mucosae between the UC-Ca and UC-NonCa groups, we could identify 40 genes that were differentially expressed between two groups. The list of discriminating genes included low-density lipoprotein receptor-related protein (LRP5 and LRP6). Previous studies suggested that LRP5 and LRP6 expression promotes cancer cell proliferation and tumorigenesis and are considered as candidate oncogenes. In the present study, both LRP5 and LRP6 showed significantly higher expression in the UC-Ca group, which suggests the importance of these genes in the development of UC-associated colorectal cancers. With the 40 selected discriminating genes, we did class prediction of the development of colorectal neoplasms in UC patients. Using the k-nearest neighbor method and the support vector machine, we could predict the development of UC-associated neoplasms with an accuracy of 86.8% and 98.1%, respectively.
These findings have important implications for the early detection of malignant lesions in UC and may provide directions for future research into the molecular mechanisms of UC-associated cancer.
溃疡性结肠炎(UC)与结直肠癌的高风险相关。为了鉴定可预测UC中癌症发生的基因,我们使用UC患者的非肿瘤性直肠黏膜进行了DNA微阵列分析。
检测了53例UC患者非肿瘤性黏膜中的基因表达。使用人类基因组U133 Plus 2.0基因芯片阵列(Affymetrix)检测基因表达谱。在53例UC患者中,10例患有UC相关癌症(UC-Ca组),而43例未患(UC-NonCa组)。
通过比较UC-Ca组和UC-NonCa组非肿瘤性直肠黏膜的基因表达谱,我们能够鉴定出两组之间差异表达的40个基因。鉴别基因列表包括低密度脂蛋白受体相关蛋白(LRP5和LRP6)。先前的研究表明,LRP5和LRP6的表达促进癌细胞增殖和肿瘤发生,被认为是候选癌基因。在本研究中,LRP5和LRP6在UC-Ca组中均表现出显著更高的表达,这表明这些基因在UC相关结直肠癌发生中的重要性。利用这40个选定的鉴别基因,我们对UC患者结直肠肿瘤的发生进行了分类预测。使用k近邻法和支持向量机,我们分别能够以86.8%和98.1%的准确率预测UC相关肿瘤的发生。
这些发现对UC恶性病变的早期检测具有重要意义,并可能为未来UC相关癌症分子机制的研究提供方向。