Gravel S, Delsol G, Al Saati T
Department of Pathology and CIGH/CNRS, CHU-Purpan, Toulouse, France.
Blood. 1998 Apr 15;91(8):2866-74.
Using the polymerase chain reaction (PCR) technique and total DNA extracts of Hodgkin's disease (HD)-involved lymph nodes, the t(14;18)(q32;q21) translocation was detected in 37 of 115 (32.2%) cases studied. No correlation was found between the presence of this translocation and bcl-2 protein expression in Hodgkin and Reed-Sternberg (HRS) cells detected by immunohistochemistry in 58 of 96 (60.4%) cases. To identify the cells carrying the t(14;18) translocation, single-cell DNA from HRS cells isolated by micromanipulation from frozen tissue sections of lymph nodes was investigated by PCR amplification. Eleven cases showing a positive band of the same size in at least two of five PCR experiments performed on the same total DNA extract were selected for single-cell PCR. We postulated that this repeated successful amplification could be indicative of the presence of the t(14;18) translocation in the neoplastic HRS cells. Single cells from frozen tumor sections of the t(14;18)-positive OCI LY8 cell line grafted into nude mice served as a positive control. The bcl-2/JH rearrangement, involved in this translocation, could be amplified from single-cell DNA of the latter tumor, whereas, in all of the HD cases, HRS cells were found to be negative. We conclude that the t(14;18) translocation is not localized in HRS cells, but in nonmalignant B bystander lymphocytes, admixed with these neoplastic cells.
利用聚合酶链反应(PCR)技术及霍奇金淋巴瘤(HD)受累淋巴结的总DNA提取物,在所研究的115例病例中的37例(32.2%)检测到t(14;18)(q32;q21)易位。在96例病例中的58例(60.4%)通过免疫组织化学检测发现,该易位的存在与霍奇金和里德-斯腾伯格(HRS)细胞中bcl-2蛋白表达之间无相关性。为了鉴定携带t(14;18)易位的细胞,对通过显微操作从淋巴结冰冻组织切片中分离出的HRS细胞的单细胞DNA进行PCR扩增研究。在对同一总DNA提取物进行的五次PCR实验中,至少两次显示出相同大小阳性条带的11例病例被选作单细胞PCR研究对象。我们推测这种反复成功的扩增可能表明肿瘤性HRS细胞中存在t(14;18)易位。将t(14;18)阳性的OCI LY8细胞系接种到裸鼠体内后,取自其冰冻肿瘤切片的单细胞作为阳性对照。参与该易位的bcl-2/JH重排可从后一种肿瘤的单细胞DNA中扩增出来,而在所有HD病例中,发现HRS细胞均为阴性。我们得出结论,t(14;18)易位并非定位于HRS细胞,而是定位于与这些肿瘤细胞混合存在的非恶性旁观者B淋巴细胞中。