Suppr超能文献

21号染色体三体在白血病发生中的作用

Trisomy of chromosome 21 in leukemogenesis.

作者信息

Izraeli Shai, Rainis Liat, Hertzberg Libi, Smooha Gil, Birger Yehudit

机构信息

Research Section of Childhood Malignancies, Department of Pediatric Hemato-Oncology, and the Sheba Cancer Research Center, Sheba Medical Hospital, Tel-Hashomer, Ramat-Gan 52621, Israel.

出版信息

Blood Cells Mol Dis. 2007 Sep-Oct;39(2):156-9. doi: 10.1016/j.bcmd.2007.04.004. Epub 2007 May 29.

Abstract

Extra copies of chromosome 21 are often found in sporadic leukemias. Constitutional trisomy 21 of Down syndrome (DS) is associated with markedly increased risk for childhood leukemia. Thus the oncogenic role of trisomy 21 in the more common sporadic childhood leukemias may be revealed through the investigations of the relatively rare leukemias of DS. Recent studies of the megakaryoblastic leukemias of Down syndrome have uncovered a developmental leukemogenic mechanism characterized by a unique pre-natal collaboration between overexpressed genes from chromosome 21 and an acquired mutation in the transcription factor GATA1. The base of the markedly enhanced risk for acute lymphoblastic leukemia conferred by trisomy 21 is still unclear. Studies of the leukemias of DS are likely to contribute to the general understanding of the oncogenic mechanisms of chromosomal aneuploidies, the most common abnormalities in cancer.

摘要

21号染色体的额外拷贝经常在散发性白血病中被发现。唐氏综合征(DS)的先天性21三体与儿童白血病风险显著增加有关。因此,通过对相对罕见的唐氏综合征白血病进行研究,可能会揭示21三体在更常见的散发性儿童白血病中的致癌作用。最近对唐氏综合征巨核细胞白血病的研究发现了一种发育性白血病发生机制,其特征是21号染色体上过度表达的基因与转录因子GATA1的获得性突变之间存在独特的产前协同作用。21三体导致急性淋巴细胞白血病风险显著增加的原因仍不清楚。对唐氏综合征白血病的研究可能有助于人们对染色体非整倍体致癌机制的总体理解,染色体非整倍体是癌症中最常见的异常情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验