参与白血病发生和造血的10个因素

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)
{"title":"参与白血病发生和造血的10个因素","authors":"MBBS, PhD, FRACP Andrew G. Elefanty (Research Scientist),&nbsp;BSc, MBBS, PhD, FRACP, FRCPA Lorraine Robb (Research Scientist),&nbsp;MBBS, PhD, FRACP, FRCPath C. Glenn Begley (Principal Research Fellow)","doi":"10.1016/S0950-3536(97)80028-5","DOIUrl":null,"url":null,"abstract":"<div><p>This review describes the chromosomal abnormalities in T-cell acute lymphoblastic leukaemia (ALL) which result in the over-expression of the gene <em>SCL</em>, which encodes a helix-loop-helix transcription factor. Also described are how gene targeting studies have revealed a key role for <em>SCL</em> 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.</p></div>","PeriodicalId":77029,"journal":{"name":"Bailliere's clinical haematology","volume":"10 3","pages":"Pages 589-614"},"PeriodicalIF":0.0000,"publicationDate":"1997-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0950-3536(97)80028-5","citationCount":"6","resultStr":"{\"title\":\"10 Factors involved in leukaemogenesis and haemopoiesis\",\"authors\":\"MBBS, PhD, FRACP Andrew G. Elefanty (Research Scientist),&nbsp;BSc, MBBS, PhD, FRACP, FRCPA Lorraine Robb (Research Scientist),&nbsp;MBBS, PhD, FRACP, FRCPath C. Glenn Begley (Principal Research Fellow)\",\"doi\":\"10.1016/S0950-3536(97)80028-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This review describes the chromosomal abnormalities in T-cell acute lymphoblastic leukaemia (ALL) which result in the over-expression of the gene <em>SCL</em>, which encodes a helix-loop-helix transcription factor. Also described are how gene targeting studies have revealed a key role for <em>SCL</em> 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.</p></div>\",\"PeriodicalId\":77029,\"journal\":{\"name\":\"Bailliere's clinical haematology\",\"volume\":\"10 3\",\"pages\":\"Pages 589-614\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0950-3536(97)80028-5\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bailliere's clinical haematology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0950353697800285\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bailliere's clinical haematology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0950353697800285","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

摘要

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。
10 Factors involved in leukaemogenesis and haemopoiesis

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信