Sundaresan V, Ganly P, Hasleton P, Bleehen N M, Rabbitts P
Medical Research Council, Clinical Oncology and Radiotherapeutics Unit, Cambridge, U.K.
J Pathol. 1993 Jan;169(1):43-52. doi: 10.1002/path.1711690108.
Loss of genetic material, corresponding to chromosomal deletions, has been detected in a wide range of tumours and may indicate the position of a tumour suppressor gene. In order to identify the position of such a gene more precisely, many tumour samples must be studied until a minimum consensus deletion is characterized. This process is particularly necessary for lung tumours in which the deletion in chromosome 3, seen with such high frequencies in all histological subtypes, is almost always large. We have recently described the use of the polymerase chain reaction (PCR) for restriction fragment length polymorphism (RFLP) analysis of DNA isolated from small bronchial biopsies of lung tumours. In this study we adapted this technique to allow genotyping of DNA isolated from paraffin wax-embedded material (PWEM) microdissected from glass slides. We have investigated 12 lung tumours at polymorphic loci on chromosome 3 and showed allelic loss in all samples. In adapting PCR-RFLP analysis for DNA isolated from PWEM, we have concentrated on those approaches which might be adaptable to routine clinical practice. Somatic genetic changes are now being identified in many tumour types, and this information is expected to be of diagnostic and prognostic significance.
在多种肿瘤中均检测到了与染色体缺失相对应的遗传物质丢失,这可能表明存在肿瘤抑制基因。为了更精确地确定此类基因的位置,必须研究许多肿瘤样本,直至确定最小的共同缺失特征。对于肺癌来说,这一过程尤为必要,因为在所有组织学亚型中,3号染色体的缺失频率都很高,而且几乎总是大片段缺失。我们最近描述了利用聚合酶链反应(PCR)对从肺癌小支气管活检样本中分离的DNA进行限制性片段长度多态性(RFLP)分析。在本研究中,我们改进了这项技术,以便对从玻片上显微切割的石蜡包埋材料(PWEM)中分离的DNA进行基因分型。我们在3号染色体的多态位点上研究了12例肺癌肿瘤,结果显示所有样本均存在等位基因缺失。在将PCR-RFLP分析应用于从PWEM中分离的DNA时,我们重点关注了那些可能适用于常规临床实践的方法。目前在许多肿瘤类型中都发现了体细胞遗传改变,预计这些信息将具有诊断和预后意义。