Kosulin Karin, Haberler Christine, Hainfellner Johannes A, Amann Gabriele, Lang Susanna, Lion Thomas
Division of Molecular Microbiology and Development of Genetic Diagnostics, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Kinderspitalgasse 6, A-1090 Vienna, Austria.
J Virol. 2007 Jul;81(14):7629-35. doi: 10.1128/JVI.00355-07. Epub 2007 May 9.
Adenoviruses (AdVs) contain genes coding for proteins with transforming potential, and certain AdV serotypes have been shown to induce tumors in rodents. However, data on the possible oncogenicity of AdVs in humans are scarce. We have therefore employed a real-time quantitative PCR (RQ-PCR) assay permitting highly sensitive detection of all 51 currently known human AdV serotypes to screen more than 500 tumor specimens derived from 17 different childhood cancer entities including leukemias, lymphomas, and solid tumors. Most tumor entities analyzed showed no evidence for the presence of AdV sequences, but AdV DNA was detected by RQ-PCR in different brain tumors including 25/30 glioblastomas, 22/30 oligodendrogliomas, and 20/30 ependymomas. Nonmalignant counterparts of AdV-positive brain tumors, including specimens of ependymal cells, plexus choroideus, and periventricular white matter, were screened for control purposes and revealed the presence of AdV DNA in most specimens tested. Identification of the AdV types present in positive malignant and nonmalignant brain tissue specimens revealed predominantly representatives of species B and D and, less commonly, C. To exclude contamination as a possible cause of false-positive results, specimens with AdV sequences detectable by PCR were subsequently analyzed by in situ hybridization, which confirmed the PCR findings in all instances. The central nervous system appears to represent a common site of AdV infection with virus persistence, thus providing the first evidence for the possible contribution of AdVs to the multistep process of tumor pathogenesis in brain tissue.
腺病毒(AdV)含有编码具有转化潜能蛋白质的基因,并且某些腺病毒血清型已被证明可在啮齿动物中诱发肿瘤。然而,关于腺病毒在人类中可能的致癌性的数据却很少。因此,我们采用了一种实时定量PCR(RQ-PCR)检测方法,该方法能够高度灵敏地检测所有51种目前已知的人类腺病毒血清型,以筛查来自17种不同儿童癌症实体(包括白血病、淋巴瘤和实体瘤)的500多个肿瘤标本。大多数分析的肿瘤实体未显示出存在腺病毒序列的证据,但通过RQ-PCR在不同的脑肿瘤中检测到了腺病毒DNA,包括25/30例胶质母细胞瘤、22/30例少突胶质细胞瘤和20/30例室管膜瘤。为了进行对照,对腺病毒阳性脑肿瘤的非恶性对应物,包括室管膜细胞、脉络丛和脑室周围白质的标本进行了筛查,结果显示大多数检测标本中存在腺病毒DNA。对阳性恶性和非恶性脑组织标本中存在的腺病毒类型进行鉴定,结果显示主要为B和D种的代表,较少见的是C种。为了排除污染作为假阳性结果的可能原因,随后对通过PCR可检测到腺病毒序列的标本进行原位杂交分析,在所有情况下均证实了PCR结果。中枢神经系统似乎是腺病毒感染并持续存在的常见部位,从而为腺病毒可能在脑组织肿瘤发病机制的多步骤过程中发挥作用提供了首个证据。