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Assessment of Epstein-Barr virus nucleic acids in gastric but not inbreast cancer by next-generation sequencing of pooled Mexican samples

机译:评估爱泼斯坦-巴尔病毒核酸在胃中而不是在胃中合并墨西哥样本的下一代测序检测乳腺癌

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摘要

Gastric (GC) and breast (BrC) cancer are two of the most common and deadly tumours. Different lines of evidence suggest a possible causative role of viral infections for both GC and BrC. Wide genome sequencing (WGS) technologies allow searching for viral agents in tissues of patients with cancer. These technologies have already contributed to establish virus-cancer associations as well as to discovery new tumour viruses. The objective of this study was to document possible associations of viral infection with GC and BrC in Mexican patients. In order to gain idea about cost effective conditions of experimental sequencing, we first carried out an in silico simulation of WGS. The next-generation-platform IlluminaGallx was then used to sequence GC and BrC tumour samples. While we did not find viral sequences in tissues from BrC patients, multiple reads matching Epstein-Barr virus (EBV) sequences were found in GC tissues. An end-point polymerase chain reaction confirmed an enrichment of EBV sequences in one of the GC samples sequenced, validating the next-generation sequencing-bioinformatics pipeline.
机译:胃癌(GC)和乳腺癌(BrC)是两种最常见和致命的肿瘤。不同的证据表明,病毒感染可能对GC和BrC都有致病作用。宽基因组测序(WGS)技术允许在癌症患者的组织中寻找病毒制剂。这些技术已经为建立病毒-癌症关联以及发现新的肿瘤病毒做出了贡献。这项研究的目的是记录墨西哥患者中病毒感染与GC和BrC的可能联系。为了获得有关实验测序的经济有效条件的想法,我们首先对WGS进行了计算机模拟。然后使用下一代平台IlluminaGallx对GC和BrC肿瘤样品进行测序。虽然我们没有在BrC患者的组织中发现病毒序列,但在GC组织中发现了多个与爱泼斯坦-巴尔病毒(EBV)序列相符的序列。端点聚合酶链反应证实了其中一种测序的GC样品中EBV序列的富集,从而验证了下一代测序生物信息学流程。

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