Lang S M, Stratakis D F, Heinzlmann M, Heldwein W, Wiebecke B, Loeschke K
Medizinische Klinik, Klinikum Innenstadt der Universität München, Department of Internal Medicine, Ziemssenstrasse 1, D-80336 München, Germany.
Gut. 1999 Jun;44(6):822-5. doi: 10.1136/gut.44.6.822.
In patients with long standing ulcerative colitis at risk of developing malignancy, mutations of the p53 and Ki-ras gene were investigated in lavage solution obtained at surveillance colonoscopy.
DNA was isolated from 31 consecutive patients with total or subtotal ulcerative colitis and a disease duration of between seven and 26 years. Twenty seven control patients showed no macroscopic or microscopic inflammation on colonoscopy. Exons 5-8 of the p53 gene and exon 1 of the Ki-ras gene were amplified by polymerase chain reaction. Mutations of the p53 gene were detected by single strand conformation polymorphism analysis. Point mutations of the Ki-ras gene were hybridised on dot blots with oligonucleotides marked with digoxigenin.
In all cases of ulcerative colitis and in all of the 27 control patients, wild type p53 and wild type Ki-ras could be detected. In four patients with ulcerative colitis, a mutation in exon 5 to 7 of the p53 gene was found, and two patients had a mutation of the Ki-ras gene (Gly to Asp-12, Gly to Val-12). None of these patients had dysplasia in serial biopsy specimens, and all but one had had the disease for more than 10 years. One control patient had a mutation.
Mutations were more frequent in patients with long standing ulcerative colitis (19%) than in control patients (3%, p = 0.07). The technique may be useful for screening for early malignancy in ulcerative colitis.
在有发生恶性肿瘤风险的长期溃疡性结肠炎患者中,对监测结肠镜检查时获取的灌洗溶液中的p53和Ki-ras基因突变进行了研究。
从31例连续性全结肠炎或次全结肠炎患者中分离DNA,病程为7至26年。27例对照患者结肠镜检查未显示宏观或微观炎症。通过聚合酶链反应扩增p53基因的外显子5至8和Ki-ras基因的外显子1。通过单链构象多态性分析检测p53基因的突变。Ki-ras基因的点突变与用地高辛标记的寡核苷酸在点杂交上进行杂交。
在所有溃疡性结肠炎病例以及所有27例对照患者中,均可检测到野生型p53和野生型Ki-ras。在4例溃疡性结肠炎患者中,发现p53基因外显子5至7发生突变,2例患者发生Ki-ras基因突变(第12位甘氨酸突变为天冬氨酸、第12位甘氨酸突变为缬氨酸)。这些患者的系列活检标本均无发育异常,除1例患者外,所有患者病程均超过10年。1例对照患者发生突变。
长期溃疡性结肠炎患者的突变发生率(19%)高于对照患者(3%,p = 0.07)。该技术可能有助于溃疡性结肠炎早期恶性肿瘤的筛查。