Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
26 11 2019
Historique:
received: 30 08 2019
accepted: 15 10 2019
entrez: 19 11 2019
pubmed: 19 11 2019
medline: 9 9 2020
Statut: ppublish

Résumé

Myelodysplastic syndromes (MDS) are hematopoietic stem cell malignancies. Known predisposing factors to adult MDS include rare germline mutations, cytotoxic therapy, age-related clonal hematopoiesis, and autoimmune or chronic inflammatory disorders. To date, no published studies characterizing MDS-associated germline susceptibility polymorphisms exist. We performed a genome-wide association study of 2 sample sets (555 MDS cases vs 2964 control subjects; 352 MDS cases vs 2640 control subjects) in non-del(5q) MDS cases of European genomic ancestry. Meta-analysis identified 8 MDS-associated loci at 1q31.1 (PLA2G4A), 3p14.1 (FAM19A4), 5q21.3 (EFNA5), 6p21.33, 10q23.1 (GRID1), 12q24.32, 15q26.1, and 20q13.12 (EYA2) that approached genome-wide significance. Gene expression for 5 loci that mapped within or near genes was significantly upregulated in MDS bone marrow cells compared with those of control subjects (P < .01). Higher PLA2G4A expression and lower EYA2 expression were associated with poorer overall survival (P = .039 and P = .037, respectively). Higher PLA2G4A expression is associated with mutations in NRAS (P < .001), RUNX1 (P = .012), ASXL1 (P = .007), and EZH2 (P = .038), all of which are known to contribute to MDS development. EYA2 expression was an independently favorable risk factor irrespective of age, sex, and Revised International Scoring System score (relative risk, 0.67; P = .048). Notably, these genes have regulatory roles in innate immunity, a critical driver of MDS pathogenesis. EYA2 overexpression induced innate immune activation, whereas EYA2 inhibition restored colony-forming potential in primary MDS cells indicative of hematopoietic restoration and possible clinical relevance. In conclusion, among 8 suggestive MDS-associated loci, 5 map to genes upregulated in MDS with functional roles in innate immunity and potential biological relevance to MDS.

Identifiants

pubmed: 31738830
pii: 428769
doi: 10.1182/bloodadvances.2019000922
pmc: PMC6880887
doi:

Types de publication

Journal Article Meta-Analysis Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3579-3589

Subventions

Organisme : NCI NIH HHS
ID : P30 CA076292
Pays : United States

Informations de copyright

© 2019 by The American Society of Hematology.

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Auteurs

Kathy L McGraw (KL)

Department of Malignant Hematology and.

Chia-Ho Cheng (CH)

Department of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, FL.

Y Ann Chen (YA)

Department of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, FL.

Hsin-An Hou (HA)

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Björn Nilsson (B)

Department of Laboratory Medicine, Section of Hematology and Transfusion Medicine, Lund University, Lund, Sweden.

Giulio Genovese (G)

Stanley Center for Psychiatric Research and.
Program in Medical and Population Genetics, Broad Institute of the Massachusetts Institute of Technology and Harvard, Cambridge, MA.
Department of Genetics, Harvard Medical School, Boston, MA.

Thomas Cluzeau (T)

Cote d'Azur University, Centre Hospitalier Universitaire of Nice, Nice, France.

Andrea Pellagatti (A)

Bloodwise Molecular Haematology Unit, Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford and Oxford Biomedical Research Centre Haematology Theme, Oxford, United Kingdom.

Bartlomiej P Przychodzen (BP)

Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH.

Mar Mallo (M)

Institut de Recerca Contra la Leucèmia Josep Carreras, Institut Catala d'Oncologia-Hospital GermansTrias i Pujol, Universitat Autonòma de Barcelona, Badalona, Barcelona, Spain.

Leonor Arenillas (L)

Laboratori de Citologia Hematòlogica, Servei de Patologia, Hospital del Mar, Barcelona, Spain.

Azim Mohamedali (A)

Department of Haematological Medicine, Kings College London, London, United Kingdom.

Lionel Adès (L)

Senior Hematology Department, Hopital Saint Louis, Paris, France.

David A Sallman (DA)

Department of Malignant Hematology and.

Eric Padron (E)

Department of Malignant Hematology and.

Lubomir Sokol (L)

Department of Malignant Hematology and.

Chimene Moreilhon (C)

Cote d'Azur University, Centre Hospitalier Universitaire of Nice, Nice, France.

Sophie Raynaud (S)

Cote d'Azur University, Centre Hospitalier Universitaire of Nice, Nice, France.

Hwei-Fang Tien (HF)

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Jacqueline Boultwood (J)

Bloodwise Molecular Haematology Unit, Nuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford and Oxford Biomedical Research Centre Haematology Theme, Oxford, United Kingdom.

Benjamin L Ebert (BL)

Departments of Medicine and Medical Oncology, Harvard Medical School and Brigham and Women's Hospital, Boston, MA; and.

Francesc Sole (F)

Institut de Recerca Contra la Leucèmia Josep Carreras, Institut Catala d'Oncologia-Hospital GermansTrias i Pujol, Universitat Autonòma de Barcelona, Badalona, Barcelona, Spain.

Pierre Fenaux (P)

Senior Hematology Department, Hopital Saint Louis, Paris, France.

Ghulam J Mufti (GJ)

Department of Haematological Medicine, Kings College London, London, United Kingdom.

Jaroslaw P Maciejewski (JP)

Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH.

Peter A Kanetsky (PA)

Department of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL.

Alan F List (AF)

Department of Malignant Hematology and.

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