Chang Y S, Tyan Y S, Liu S T, Tsai M S, Pao C C
Department of Microbiology and Immunology, Chang-Gung Medical College, Taoyuan, Taiwan, Republic of China.
J Clin Microbiol. 1990 Nov;28(11):2398-402. doi: 10.1128/jcm.28.11.2398-2402.1990.
The presence of Epstein-Barr virus (EBV) DNA sequences was examined by the polymerase chain reaction in 50 nasopharyngeal carcinoma (NPC) biopsy specimens and in two primary epithelial tumor cell cultures derived from patients with NPC. The detection limit was a single EBV genome equivalent by agarose gel electrophoresis followed by Southern blot analysis of the amplified products. EBV DNA sequences were detected in all 41 undifferentiated NPC cell specimens, in 2 of 4 moderately differentiated NPC cell specimens, and in 3 of 5 keratinized NPC cell specimens. Undifferentiated NPC cells were also found to contain higher copy numbers of EBV than cells of the other two types of NPC. Our data suggest that EBV replication may be closely associated with the differentiation of NPC tumor cells. The results also demonstrated a sensitive and specific method for the detection of EBV DNA sequences in NPC tumor cells.
采用聚合酶链反应检测了50份鼻咽癌(NPC)活检标本以及源自NPC患者的两种原发性上皮肿瘤细胞培养物中Epstein-Barr病毒(EBV)DNA序列的存在情况。通过琼脂糖凝胶电泳,随后对扩增产物进行Southern印迹分析,检测限为单个EBV基因组当量。在所有41份未分化NPC细胞标本、4份中度分化NPC细胞标本中的2份以及5份角化NPC细胞标本中的3份中检测到EBV DNA序列。还发现未分化NPC细胞所含EBV拷贝数高于其他两种类型NPC的细胞。我们的数据表明,EBV复制可能与NPC肿瘤细胞的分化密切相关。结果还证明了一种检测NPC肿瘤细胞中EBV DNA序列的灵敏且特异的方法。