Miyamura K, Kobayashi T, Sasaki T, Ibuka T, Imai K, Sakai Y, Kawaguchi K, Miyashita T, Iwaya M, Mizutani S
Department of Chemotherapy, Tokyo Metropolitan Komagome Hospital, Japan.
Int J Hematol. 1991 Apr;54(2):137-40.
Twenty cases of Japanese non-Hodgkin's lymphoma with B cell markers were studied with respect to their immunoglobulin heavy (IgH) chain gene loci on chromosome 14 and BCL2 loci on chromosome 18. All of the 20 cases showed IgH gene rearrangement on at least one of the alleles. Molecular analysis using two chromosome 18-specific DNA probes (pFL1 and pFL2) showed rearrangement of the BCL2 region in three of 20 cases. As these three samples showed the rearranged allele of the IgH gene comigrating with that of the BCL2 gene, polymerase chain reaction (PCR) was carried out to amplify the juncture between IgJH on chromosome 14 and BCL2 on chromosome 18. In all of these three cases, gene amplification between the two loci was found to occur, indicating that molecular mechanisms involved in this type of chromosomal translocation in Japan might be similar to cases in the United States (U.S.) in a limited number of cases. Furthermore, this amplification technique revealed minimal tumor cells circulating in peripheral blood, even though lymphoma cells could not be identified morphologically. Thus, the PCR technique is useful for both the detection of minimal tumor cells as well as for the determination of the molecular nature of chromosomal translocation in some of Japanese cases.
对20例具有B细胞标志物的日本非霍奇金淋巴瘤患者,研究了其14号染色体上的免疫球蛋白重链(IgH)基因位点和18号染色体上的BCL2基因位点。20例患者均至少在一个等位基因上出现了IgH基因重排。使用两种18号染色体特异性DNA探针(pFL1和pFL2)进行分子分析,结果显示20例中有3例存在BCL2区域重排。由于这3个样本显示IgH基因的重排等位基因与BCL2基因的重排等位基因共迁移,因此进行了聚合酶链反应(PCR)以扩增14号染色体上的IgJH与18号染色体上的BCL2之间的连接点。在所有这3例病例中,均发现两个位点之间发生了基因扩增,这表明在日本,这种类型染色体易位所涉及的分子机制在少数病例中可能与美国的病例相似。此外,尽管在外周血中无法通过形态学鉴定淋巴瘤细胞,但这种扩增技术显示外周血中循环的肿瘤细胞极少。因此,PCR技术对于检测微小肿瘤细胞以及确定部分日本病例中染色体易位的分子性质均很有用。