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急性白血病中的11q23重排

11q23 rearrangements in acute leukemia.

作者信息

Rubnitz J E, Behm F G, Downing J R

机构信息

Department of Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

Leukemia. 1996 Jan;10(1):74-82.

PMID:8558942
Abstract

The MLL gene, located at chromosome 11, band q23, is frequently disrupted by a variety of chromosomal rearrangements that occur in acute lymphoblastic leukemias and in a subset of de novo and secondary acute myeloid leukemias. In both scenarios, MLL rearrangements are associated with distinct clinical features and a poor prognosis. MLL encodes a large protein (MLL) that shares homology with the Drosophila trithorax protein. 11q23 translocations result in the generation of a series of acute leukemia-specific chimeric proteins that contain the N-terminus of MLL and are thought to be crucial to leukemogenesis. In this article, we review the structural features of the MLL fusion proteins as well as the clinical features and molecular diagnosis of acute leukemias containing MLL arrangements.

摘要

MLL基因位于11号染色体q23带,在急性淋巴细胞白血病以及一部分原发性和继发性急性髓细胞白血病中,常因各种染色体重排而发生断裂。在这两种情况下,MLL重排均与独特的临床特征及不良预后相关。MLL编码一种与果蝇三体胸蛋白具有同源性的大型蛋白质(MLL)。11q23易位导致产生一系列急性白血病特异性嵌合蛋白,这些蛋白含有MLL的N端,被认为对白血病发生至关重要。在本文中,我们综述了MLL融合蛋白的结构特征以及含有MLL重排的急性白血病的临床特征和分子诊断。

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