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应用聚合酶链反应技术检测鼻咽癌中的爱泼斯坦-巴尔病毒和人乳头瘤病毒

Detection of Epstein-Barr virus and human papillomavirus in nasopharyngeal carcinoma by the polymerase chain reaction technique.

作者信息

Giannoudis A, Ergazaki M, Segas J, Giotakis J, Adamopoulos G, Gorgoulis V, Spandidos D A

机构信息

Institute of Biological Research and Biotechnology, National Hellenic Research Foundation, Athens, Greece.

出版信息

Cancer Lett. 1995 Mar 2;89(2):177-81. doi: 10.1016/0304-3835(94)03667-8.

Abstract

We used the PCR technique to detect the Epstein-Barr virus (EBV) and human papillomavirus (HPV) DNA in paraffin-embedded tissues from Greek patients with nasopharyngeal carcinoma (NPC). The oligonucleotide primers used for the detection of EBV amplify a 375-bp long sequence from the EcoRI B fragment of the viral genome, whereas for HPV the primers amplify a 151-bp long sequence of the viral genome. The PCR products were analysed by agarose gel electrophoresis and visualised by UV illumination after staining with ethidium bromide. Sixty-three specimens were examined. EBV specific sequence was amplified in 20 (32%) and HPV in 12 (19%) out of the 63 samples. There was no co-infection with EBV and HPV. Although there is a high correlation of EBV infection with poorly differentiated NPC in patients from Southern China and South-East Asia, the restricted distribution suggests genetic or environmental cofactors in the development of the neoplasm. Our results confirm this suggestion since there was only a 32% correlation of EBV with NPC in Greece. HPV may also be involved in the carcinogenesis of EBV-negative squamous cell nasopharyngeal carcinomas.

摘要

我们运用聚合酶链反应(PCR)技术,检测了来自希腊鼻咽癌(NPC)患者石蜡包埋组织中的爱泼斯坦-巴尔病毒(EBV)和人乳头瘤病毒(HPV)DNA。用于检测EBV的寡核苷酸引物,可从病毒基因组的EcoRI B片段扩增出一段375bp长的序列,而用于HPV的引物则可扩增出一段151bp长的病毒基因组序列。PCR产物通过琼脂糖凝胶电泳进行分析,并用溴化乙锭染色后经紫外线照射显影。共检测了63个标本。63个样本中,有20个(32%)扩增出了EBV特异性序列,12个(19%)扩增出了HPV特异性序列。未发现EBV和HPV的合并感染。尽管在中国南方和东南亚患者中,EBV感染与低分化NPC高度相关,但分布受限表明肿瘤发生过程中存在遗传或环境协同因素。我们的结果证实了这一推测,因为在希腊,EBV与NPC的相关性仅为32%。HPV也可能参与EBV阴性的鳞状细胞鼻咽癌的致癌过程。

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