Haematopoietic development and leukaemia in Down syndrome

Children with constitutional trisomy 21 (cT21, Down Syndrome, DS) are at a higher risk for both myeloid and B-lymphoid leukaemias. The myeloid leukaemias are often preceded by a transient neonatal pre-leukaemic syndrome, Transient Abnormal Myelopoiesis (TAM). TAM is caused by cooperation between cT2...

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Main Authors: Roberts, I, Izraeli, S
Format: Journal article
Language:English
Published: Wiley 2014
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author Roberts, I
Izraeli, S
author_facet Roberts, I
Izraeli, S
author_sort Roberts, I
collection OXFORD
description Children with constitutional trisomy 21 (cT21, Down Syndrome, DS) are at a higher risk for both myeloid and B-lymphoid leukaemias. The myeloid leukaemias are often preceded by a transient neonatal pre-leukaemic syndrome, Transient Abnormal Myelopoiesis (TAM). TAM is caused by cooperation between cT21 and acquired somatic N-terminal truncating mutations in the key haematopoietic transcription factor GATA1. These mutations, which are not leukaemogenic in the absence of cT21, are found in almost one-third of neonates with DS. Analysis of primary human fetal liver haematopoietic cells and of human embryonic stem cells demonstrates that cT21 itself substantially alters human fetal haematopoietic development. Consequently, many haematopoietic developmental defects are observed in neonates with DS even in the absence of TAM. Although studies in mouse models have suggested a pathogenic role of deregulated expression of several chromosome 21-encoded genes, their role in human leukaemogenesis remains unclear. As cT21 exists in all embryonic cells, the molecular basis of cT21-associated leukaemias probably reflects a complex interaction between deregulated gene expression in haematopoietic cells and the fetal haematopoietic microenvironment in DS.
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spelling oxford-uuid:1826d9c2-5b44-4119-a98a-d3f40723d6c12024-01-09T09:34:00ZHaematopoietic development and leukaemia in Down syndromeJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:1826d9c2-5b44-4119-a98a-d3f40723d6c1EnglishSymplectic Elements at OxfordWiley2014Roberts, IIzraeli, SChildren with constitutional trisomy 21 (cT21, Down Syndrome, DS) are at a higher risk for both myeloid and B-lymphoid leukaemias. The myeloid leukaemias are often preceded by a transient neonatal pre-leukaemic syndrome, Transient Abnormal Myelopoiesis (TAM). TAM is caused by cooperation between cT21 and acquired somatic N-terminal truncating mutations in the key haematopoietic transcription factor GATA1. These mutations, which are not leukaemogenic in the absence of cT21, are found in almost one-third of neonates with DS. Analysis of primary human fetal liver haematopoietic cells and of human embryonic stem cells demonstrates that cT21 itself substantially alters human fetal haematopoietic development. Consequently, many haematopoietic developmental defects are observed in neonates with DS even in the absence of TAM. Although studies in mouse models have suggested a pathogenic role of deregulated expression of several chromosome 21-encoded genes, their role in human leukaemogenesis remains unclear. As cT21 exists in all embryonic cells, the molecular basis of cT21-associated leukaemias probably reflects a complex interaction between deregulated gene expression in haematopoietic cells and the fetal haematopoietic microenvironment in DS.
spellingShingle Roberts, I
Izraeli, S
Haematopoietic development and leukaemia in Down syndrome
title Haematopoietic development and leukaemia in Down syndrome
title_full Haematopoietic development and leukaemia in Down syndrome
title_fullStr Haematopoietic development and leukaemia in Down syndrome
title_full_unstemmed Haematopoietic development and leukaemia in Down syndrome
title_short Haematopoietic development and leukaemia in Down syndrome
title_sort haematopoietic development and leukaemia in down syndrome
work_keys_str_mv AT robertsi haematopoieticdevelopmentandleukaemiaindownsyndrome
AT izraelis haematopoieticdevelopmentandleukaemiaindownsyndrome