Advances in germline predisposition to acute leukaemias and myeloid neoplasms

Although much work has focused on the elucidation of somatic alterations that drive the development of acute leukaemias and other haematopoietic diseases, it has become increasingly recognized that germline mutations are common in many of these neoplasms. In this Review, we highlight the different g...

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Vydáno v:	Nature reviews. Cancer Ročník 21; číslo 2; s. 122 - 137
Hlavní autoři:	Klco, Jeffery M, Mullighan, Charles G
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	England Nature Publishing Group 01.02.2021
Témata:	Acute lymphoblastic leukemia Acute myeloid leukemia Blood cancer Children Disease Progression Genetic Predisposition to Disease - genetics Germ-Line Mutation - genetics Hematology Humans Leukemia Leukemia, Myeloid, Acute - genetics Mutation Myelodysplastic syndrome Myelodysplastic syndromes Myelodysplastic Syndromes - genetics p53 Protein Phenotype Phenotypes Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics Runx1 protein Tumors Uranium
ISSN:	1474-175X, 1474-1768, 1474-1768
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Shrnutí:	Although much work has focused on the elucidation of somatic alterations that drive the development of acute leukaemias and other haematopoietic diseases, it has become increasingly recognized that germline mutations are common in many of these neoplasms. In this Review, we highlight the different genetic pathways impacted by germline mutations that can ultimately lead to the development of familial and sporadic haematological malignancies, including acute lymphoblastic leukaemia, acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS). Many of the genes disrupted by somatic mutations in these diseases (for example, TP53, RUNX1, IKZF1 and ETV6) are the same as those that harbour germline mutations in children and adolescents who develop these malignancies. Moreover, the presumption that familial leukaemias only present in childhood is no longer true, in large part due to the numerous studies demonstrating germline DDX41 mutations in adults with MDS and AML. Lastly, we highlight how different cooperating events can influence the ultimate phenotype in these different familial leukaemia syndromes.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23
ISSN:	1474-175X 1474-1768 1474-1768
DOI:	10.1038/s41568-020-00315-z