Literature DB >> 28580501

Predispositions to Leukemia in Down Syndrome and Other Hereditary Disorders.

Satoshi Saida1,2,3.   

Abstract

OPINION STATEMENT: Leukemia is the most common pediatric cancer and accounts for approximately one third of childhood malignancies. There are germline genetic alterations that significantly increase the risk of developing hematopoietic malignancies in childhood. In this review, we describe a number of these hereditary disorders and their clinical features. These predispositions to cancer syndromes can be attributed to DNA repair/genetic instability, RAS pathway dysfunction, bone marrow failure, telomeropathies, immunodeficiencies, transcription factor abnormalities, pure familial leukemia, and aneuploidy. We focus especially on acute myeloid leukemia associated with Down syndrome, but also include other hereditary syndromes in this review. Recent advances in high-throughput genotyping technology have identified new genetic variations prone to human leukemia. Understanding of the mechanism of leukemia development in these hereditary syndromes allows us to gain insight into leukemogenesis in general and suggests therapeutic strategies based on these findings.

Entities:  

Keywords:  Down syndrome; Leukemia; Predisposition; TAM; Transient leukemia

Mesh:

Substances:

Year:  2017        PMID: 28580501     DOI: 10.1007/s11864-017-0485-x

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  74 in total

Review 1.  Inherited genetic variation in childhood acute lymphoblastic leukemia.

Authors:  Takaya Moriyama; Mary V Relling; Jun J Yang
Journal:  Blood       Date:  2015-05-21       Impact factor: 22.113

Review 2.  RAS diseases in children.

Authors:  Charlotte M Niemeyer
Journal:  Haematologica       Date:  2014-11       Impact factor: 9.941

3.  Risks of leukaemia and solid tumours in individuals with Down's syndrome.

Authors:  H Hasle; I H Clemmensen; M Mikkelsen
Journal:  Lancet       Date:  2000-01-15       Impact factor: 79.321

Review 4.  Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.

Authors:  K Paulsson; B Johansson
Journal:  Pathol Biol (Paris)       Date:  2006-05-11

5.  Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases.

Authors:  L Seghezzi; E Maserati; A Minelli; C Dellavecchia; P Addis; F Locatelli; A Angioni; P Balloni; C Miano; P Cavalli; C Danesino; F Pasquali
Journal:  Genes Chromosomes Cancer       Date:  1996-10       Impact factor: 5.006

6.  Mutation of CEBPA in familial acute myeloid leukemia.

Authors:  Matthew L Smith; Jamie D Cavenagh; T Andrew Lister; Jude Fitzgibbon
Journal:  N Engl J Med       Date:  2004-12-02       Impact factor: 91.245

7.  Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D).

Authors:  H F A Vasen; Z Ghorbanoghli; F Bourdeaut; O Cabaret; O Caron; A Duval; N Entz-Werle; Y Goldberg; D Ilencikova; C P Kratz; N Lavoine; J Loeffen; F H Menko; M Muleris; G Sebille; C Colas; B Burkhardt; L Brugieres; K Wimmer
Journal:  J Med Genet       Date:  2014-02-20       Impact factor: 6.318

8.  Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder.

Authors:  Jürgen Groet; Suzanne McElwaine; Monica Spinelli; Andrea Rinaldi; Ingo Burtscher; Claire Mulligan; Afua Mensah; Simona Cavani; Franca Dagna-Bricarelli; Giuseppe Basso; Finbarr E Cotter; Dean Nizetic
Journal:  Lancet       Date:  2003-05-10       Impact factor: 79.321

9.  Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families.

Authors:  Lisa Mirabello; Elizabeth R Macari; Lea Jessop; Steven R Ellis; Timothy Myers; Neelam Giri; Alison M Taylor; Katherine E McGrath; Jessica M Humphries; Bari J Ballew; Meredith Yeager; Joseph F Boland; Ji He; Belynda D Hicks; Laurie Burdett; Blanche P Alter; Leonard Zon; Sharon A Savage
Journal:  Blood       Date:  2014-05-14       Impact factor: 25.476

10.  Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.

Authors:  Blanche P Alter; Neelam Giri; Sharon A Savage; Philip S Rosenberg
Journal:  Haematologica       Date:  2017-10-19       Impact factor: 9.941

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  3 in total

Review 1.  Hematological Malignancies in Adults With a Family Predisposition.

Authors:  Tilmann Bochtler; Georg-Martin Haag; Sarah Schott; Matthias Kloor; Alwin Krämer; Carsten Müller-Tidow
Journal:  Dtsch Arztebl Int       Date:  2018-12-14       Impact factor: 5.594

2.  Missed Down Syndrome Cases after First Trimester False-Negative Screening-Lessons to be Learned.

Authors:  Anca Angela Simionescu; Ana Maria Alexandra Stanescu
Journal:  Medicina (Kaunas)       Date:  2020-04-23       Impact factor: 2.430

3.  Differential microRNA expression profile in blood of children with Down syndrome suggests a role in immunological dysfunction.

Authors:  Joice Matos Biselli; Bruna Lancia Zampieri; Patrícia Matos Biselli-Chicote; Jorge Estefano Santana de Souza; Matheus Carvalho Bürger; Wilson Araújo da Silva; Eny Maria Goloni-Bertollo; Érika Cristina Pavarino
Journal:  Hum Cell       Date:  2022-01-20       Impact factor: 4.374

  3 in total

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