Miyamoto H, Kubota Y, Shuin T, Torigoe S, Hosaka M, Iwasaki Y, Danenberg K, Danenberg P V
Department of Urology, Yokohama City University School of Medicine, Japan.
Oncol Res. 1993;5(6-7):245-9.
Mutations in the tumor suppressor gene p53 have been detected in many tumors. p53 gene mutations are also known to be involved in the progression of human bladder cancers. We investigated structural alterations in the entire coding region of the p53 gene in primary human bladder cancers, using polymerase chain reaction and single-strand conformational polymorphism analysis of RNA. Of 25 samples obtained from patients, 6 (24%) were found to have p53 alterations. DNA sequencing of the PCR products revealed 6 point mutations resulting in single amino-acid substitutions in the regions of exons 5, 6, 7, 8, and 10 of this gene, respectively. Five of 6 cases with p53 mutations were invasive, with metastasis or high-grade tumors. Interestingly, the one remaining case was a recurrent, low-grade, and superficial (pTa) tumor. In this early stage tumor, allelic loss of the p53 gene was also found, using a polymerase chain reaction-based restriction fragment length polymorphism assay. Our findings are in agreement with previous observations that p53 mutations occurred in a high percentage of high grade or invasive bladder cancers. Since mutation and allelic loss of the p53 gene were also detected in a low-grade and low-stage tumor in the present study, it is suggested that the p53 gene is involved in early stages of some bladder cancers as well as in their late stages.
在许多肿瘤中都检测到了肿瘤抑制基因p53的突变。已知p53基因突变也与人类膀胱癌的进展有关。我们使用聚合酶链反应和RNA的单链构象多态性分析,研究了原发性人类膀胱癌中p53基因整个编码区的结构改变。在从患者获取的25个样本中,发现6个(24%)存在p53改变。对PCR产物进行DNA测序发现6个点突变,分别导致该基因外显子5、6、7、8和10区域的单个氨基酸替换。6例p53突变病例中有5例为浸润性,伴有转移或高级别肿瘤。有趣的是,剩下的1例是复发性、低级别和表浅(pTa)肿瘤。在这个早期肿瘤中,使用基于聚合酶链反应的限制性片段长度多态性分析也发现了p53基因的等位基因缺失。我们的发现与之前的观察结果一致,即p53突变在高比例的高级别或浸润性膀胱癌中发生。由于在本研究的低级别和低分期肿瘤中也检测到了p53基因的突变和等位基因缺失,提示p53基因不仅参与某些膀胱癌的晚期阶段,也参与其早期阶段。