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Prenatal adenovirus infection, inhibition of DNA repair, and childhood leukemia

Prenatal adenovirus infection, inhibition of DNA repair, and childhood leukemia
产前腺病毒感染、DNA 修复抑制和儿童白血病
批准号:
8212400
负责人:
David Arnold Ornelles
金额:
$40.99万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-20 至 2014-01-31

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中文摘要
翻译
描述(由申请人提供):急性白血病是儿童最常见的恶性肿瘤,长期以来被怀疑具有感染性病因。我们假设常见的C种腺病毒是一些急性儿童白血病的起始步骤。这一假设是基于这样一种观察,即C种腺病毒DNA在后来发展为急性淋巴细胞白血病的新生儿的血液中比在未发展为白血病的儿童的血液中更常见。Ornelles和Gooding实验室的观察结果进一步证实,腺病毒感染淋巴样祖细胞可产生携带易位细胞的扩增克隆,这是儿童白血病发展的起点。本申请中提出的研究将通过以下具体目的来检验这一假设:(1)利用存档的Guthrie卡和新鲜脐带血评估产前感染C种腺病毒、白血病相关易位的发生和最终发展为白血病之间的一致性。(2)探讨腺病毒对淋巴样细胞dna修复的影响。(3)确定腺病毒感染对淋巴细胞DNA完整性的影响。(4)评价腺病毒在白血病细胞和造血祖细胞中的复制和细胞病理学。本申请中提出的研究将直接测试C种腺病毒感染是导致儿童白血病的一系列事件中的一个步骤的可能性。此外,这项工作将确定影响淋巴样细胞中腺病毒复制的细胞基因,并确定产前感染这种病毒的频率。这些研究可能为几种病毒在人类肿瘤发生中的肇事逃逸机制提供支持。公共卫生相关性:这些实验将确定一种常见且相对无害的病毒腺病毒是否有可能导致急性儿童白血病。这些研究将促进我们对腺病毒生物学的许多方面的理解,包括这种病毒在白细胞中的鲜为人知的复制周期和新生儿腺病毒感染的频率。这项工作可以为早期检测提供基础,并有助于开发一种针对最常见的儿童癌症的简单治疗方法。
英文摘要
DESCRIPTION (provided by applicant): Acute leukemias, the most common malignancy of childhood, have long been suspected of having an infectious etiology. We hypothesize that the common species C adenoviruses are responsible for the initiating step in some acute childhood leukemias. This hypothesis is based on the observation that species C adenovirus DNA is more frequently found in the blood of newborn children that later develop acute lymphoblastic leukemia than in the blood of children that do not develop leukemia. Additional support derives from observations made in the Ornelles and Gooding laboratories indicating that adenovirus infection of a lymphoid progenitor cell could produce the expanded clones of translocation-bearing cells that are the starting point for leukemia development in children. Studies proposed in this application will test this hypothesis through the following specific aims: (1) To evaluate the coincidence between prenatal infection with species C adenovirus, the occurrence of leukemia-associated translocations, and the eventual development of leukemia using archived Guthrie cards and fresh cord blood. (2) To elucidate the impact of adenovirus on DNA-repair in lymphoid cells. (3) To determine the impact of adenovirus infection on the integrity of lymphocyte cell DNA. (4) To evaluate adenovirus replication and the cytopathology of adenovirus in leukemic cells and hematopoietic progenitor cells. The studies proposed in this application will test directly the possibility that species C adenovirus infection is one step in the sequence of events leading to childhood leukemia. In addition, this work will identify cellular genes that affect adenovirus replication in lymphoid cells and determine the frequency of prenatal infection with this virus. These studies may provide support for hit-and-run mechanisms, that have been postulated for several viruses, in human oncogenesis. PUBLIC HEALTH RELEVANCE: These experiments will determine if a common and relatively innocuous virus, adenovirus, has the potential to contribute to acute childhood leukemia. These studies will advance our understanding of many aspects of adenovirus biology including the little known replication cycle of this virus in white blood cells and the frequency of adenovirus infections in the newborn. This work could provide the basis for early testing as well as help develop a simple treatment for the most common cancer of children.
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Prenatal adenovirus infection, inhibition of DNA repair, and childhood leukemia
Prenatal adenovirus infection, inhibition of DNA repair, and childhood leukemia
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Prenatal adenovirus infection, inhibition of DNA repair, and childhood leukemia
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