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[遗传性血液系统恶性肿瘤的遗传学]

[Genetics of hereditary hematological malignancies].

作者信息

Takagi Masatoshi

机构信息

Department of Pediatrics and Developmental Biology, Graduate school, Tokyo Medical and Dental University.

出版信息

Rinsho Ketsueki. 2015 Oct;56(10):1969-77. doi: 10.11406/rinketsu.56.1969.

Abstract

Familial predisposition to hematological malignancies has been recognized. Some of these malignancies are part of a well-characterized familial cancer predisposition syndrome, while others are independent of cancer predisposition, and demonstrate unique familial leukemia/lymphoma syndromes. Primary immunodeficiency is also strongly associated with the development of lymphoid malignancy. Primary immunodeficiency and leukemia/lymphoma are based on the same concept, which involves differentiation blockage. Bone marrow failure syndrome is also known to be associated with susceptibility to hematological malignancy development. Bone marrow failure syndrome exhibiting myeloid differentiation is also characterized as an aspect of primary immunodeficiency. Recent progress in genome wide association studies (GWAS) identified several single nucleotide polymorphisms (SNP) associated with leukemia/lymphoma development. Some of these genes were found to be functionally related to hematological malignancies. These discoveries are contributing to elucidation of the genetic background of leukemia/lymphoma development.

摘要

血液系统恶性肿瘤的家族易感性已得到公认。其中一些恶性肿瘤是特征明确的家族性癌症易感性综合征的一部分,而其他一些则与癌症易感性无关,并表现出独特的家族性白血病/淋巴瘤综合征。原发性免疫缺陷也与淋巴系统恶性肿瘤的发生密切相关。原发性免疫缺陷和白血病/淋巴瘤基于相同的概念,即涉及分化阻滞。骨髓衰竭综合征也已知与血液系统恶性肿瘤发生的易感性有关。表现为髓系分化的骨髓衰竭综合征也被视为原发性免疫缺陷的一个方面。全基因组关联研究(GWAS)的最新进展确定了几个与白血病/淋巴瘤发生相关的单核苷酸多态性(SNP)。其中一些基因被发现与血液系统恶性肿瘤在功能上相关。这些发现有助于阐明白血病/淋巴瘤发生的遗传背景。

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