10 Factors involved in leukaemogenesis and haemopoiesis

MBBS, PhD, FRACP Andrew G. Elefanty (Research Scientist), BSc, MBBS, PhD, FRACP, FRCPA Lorraine Robb (Research Scientist), MBBS, PhD, FRACP, FRCPath C. Glenn Begley (Principal Research Fellow)
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引用次数: 6

Abstract

This review describes the chromosomal abnormalities in T-cell acute lymphoblastic leukaemia (ALL) which result in the over-expression of the gene SCL, which encodes a helix-loop-helix transcription factor. Also described are how gene targeting studies have revealed a key role for SCL in normal haemopoiesis. Next, the BCR-ABL fusion protein, seen in chronic myeloid leukaemia (CML) and in some patients with ALL, is discussed. Finally, the involvement of members of the core-binding factor (CBF) gene family in leukaemogenesis are described. Members of this gene family are involved in the generation of fusion proteins as a result of t(8;21) and inv(16), the most common translocations associated with acute myeloid leukaemia (AML). They provide a useful model of the way in which aberrant transcriptional function, brought about through genetic alterations, can modify haemopoietic development.

参与白血病发生和造血的10个因素
本文综述了t细胞急性淋巴细胞白血病(ALL)的染色体异常,导致编码螺旋环螺旋转录因子的基因SCL过表达。还描述了基因靶向研究如何揭示了SCL在正常造血中的关键作用。接下来,讨论BCR-ABL融合蛋白在慢性髓性白血病(CML)和一些ALL患者中的表现。最后,核心结合因子(CBF)基因家族成员在白血病发生中的参与被描述。由于t(8;21)和inv(16),该基因家族的成员参与融合蛋白的产生,这是与急性髓性白血病(AML)相关的最常见的易位。它们提供了一种有用的模型,说明基因改变带来的异常转录功能可以改变造血发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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