Konishi N, Hiasa Y, Nakamura M, Kitahori Y, Matsubara K, Nagai H
Second Department of Pathology, Nara Medical University, Japan.
Am J Pathol. 1997 Jan;150(1):305-14.
Alterations in the genomic DNAs of six heterogeneous prostate carcinomas, as well as that of individual and histologically distinct foci within the tumors, were examined using restriction landmark genomic scanning, a method employing two-dimensional gel analysis of a large number of DNA fragments generated by digestion with highly specific endonucleases. Upon autoradiographic imaging, these fragments appear as spots of varying intensity and location specific for each sample. In our study, comparison of cancer DNAs against normal prostate DNA controls yielded alterations in at least 35 spots. Despite differences in the histological grading of tumors, 3 spots common to all tumor samples showed consistent amplification of intensity and 8 other common spots demonstrated consistent reduction of intensity when compared with control. In addition, spot alterations occurred between histologically identical foci isolated from within single tumors. We suggest that these spot changes detected in DNA profiles generated by restriction landmark genomic scanning reflect aberrations in as yet unidentified oncogenes and tumor suppressor genes and indicate that prostate cancer is not only histologically heterogeneous and multifocal but also genetically multicentric.
使用限制性内切酶基因组扫描技术检测了6例异质性前列腺癌的基因组DNA,以及肿瘤内单个和组织学上不同的病灶的基因组DNA。该技术是一种对大量由高特异性内切酶消化产生的DNA片段进行二维凝胶分析的方法。在放射自显影片成像时,这些片段表现为每个样品特有的强度和位置不同的斑点。在我们的研究中,将癌DNA与正常前列腺DNA对照进行比较,发现至少35个斑点有改变。尽管肿瘤的组织学分级不同,但与对照相比,所有肿瘤样品共有的3个斑点显示强度一致增加,另外8个共有的斑点显示强度一致降低。此外,从单个肿瘤中分离出的组织学相同的病灶之间也出现了斑点改变。我们认为,通过限制性内切酶基因组扫描产生的DNA图谱中检测到的这些斑点变化反映了尚未确定的癌基因和肿瘤抑制基因的畸变,表明前列腺癌不仅在组织学上是异质性和多灶性的,而且在基因上也是多中心的。