Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium
Jazyk angličtina Země Spojené státy americké Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
32678078
PubMed Central
PMC7366925
DOI
10.1038/s41408-020-00341-y
PII: 10.1038/s41408-020-00341-y
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie etiologie metabolismus patologie MeSH
- alely MeSH
- dospělí MeSH
- frekvence genu MeSH
- genetická predispozice k nemoci MeSH
- genetická variace * MeSH
- genotyp MeSH
- hodnocení rizik MeSH
- imunita genetika MeSH
- imunomodulace genetika MeSH
- jednonukleotidový polymorfismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- náchylnost k nemoci * imunologie MeSH
- nádorové biomarkery MeSH
- rizikové faktory MeSH
- senioři MeSH
- steroidy metabolismus MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- nádorové biomarkery MeSH
- steroidy MeSH
The purpose of this study was to conduct a two-stage case control association study including 654 acute myeloid leukaemia (AML) patients and 3477 controls ascertained through the NuCLEAR consortium to evaluate the effect of 27 immune-related single nucleotide polymorphisms (SNPs) on AML risk. In a pooled analysis of cohort studies, we found that carriers of the IL13rs1295686A/A genotype had an increased risk of AML (PCorr = 0.0144) whereas carriers of the VEGFArs25648T allele had a decreased risk of developing the disease (PCorr = 0.00086). In addition, we found an association of the IL8rs2227307 SNP with a decreased risk of developing AML that remained marginally significant after multiple testing (PCorr = 0.072). Functional experiments suggested that the effect of the IL13rs1295686 SNP on AML risk might be explained by its role in regulating IL1Ra secretion that modulates AML blast proliferation. Likewise, the protective effect of the IL8rs2227307 SNP might be mediated by TLR2-mediated immune responses that affect AML blast viability, proliferation and chemorresistance. Despite the potential interest of these results, additional functional studies are still warranted to unravel the mechanisms by which these variants modulate the risk of AML. These findings suggested that IL13, VEGFA and IL8 SNPs play a role in modulating AML risk.
Centre for Individualised Infection Medicine Hannover Germany
Department of Genetics University of Pisa Pisa Italy
Department of Medicine University of Granada Granada Spain
Division of Cancer Epidemiology German Cancer Research Centre 69120 Heidelberg Germany
Division of Hygiene and Medical Microbiology Medical University of Innsbruck Innsbruck Austria
Division of Molecular Genetic Epidemiology German Cancer Research Center Heidelberg Germany
Division of Pediatric Neurooncology German Cancer Research Center Heidelberg Germany
Genomic Epidemiology Group German Cancer Research Center Heidelberg Germany
Hematology department Hospital Clinico Universitario INCLIVA University of Valencia Valencia Spain
Hematology department Hospital del Mar Barcelona Spain
Hematology department University Hospital of Salamanca Salamanca Spain
Hematology department Virgen de las Nieves University Hospital Granada Spain
Hopp Children's Cancer Center Heidelberg Germany
ICVS 3B's PT Government Associate Laboratory Braga Guimarães Guimarães Portugal
Immunology department Virgen de las Nieves University Hospital Granada Spain
Institute of Cancer Research Department of Medicine 1 Medical University of Vienna Vienna Austria
Istituto di Ematologia Università Cattolica del S Cuore Rome Italy
Life and Health Sciences Research Institute School of Medicine University of Minho Braga Portugal
Rheumatology and Metabolic Bone Diseases department Hospital de Santa Maria CHLN Lisbon Portugal
Universitätsklinikum Würzburg Medizinische Klinik 2 Würzburg Germany
Zobrazit více v PubMed
Estey E, Dohner H. Acute myeloid leukaemia. Lancet. 2006;368:1894–1907. PubMed
De Kouchkovsky I, Abdul-Hay M. ‘Acute myeloid leukemia: a comprehensive review and 2016 update’. Blood Cancer J. 2016;6:e441. PubMed PMC
Dohner H, et al. Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. Blood. 2017;129:424–447. PubMed PMC
Dohner K, et al. Impact of NPM1/FLT3-ITD genotypes defined by the 2017 European LeukemiaNet in patients with acute myeloid leukemia. Blood. 2020;135:371–380. PubMed PMC
Vago L, Gojo I. Immune escape and immunotherapy of acute myeloid leukemia. J. Clin. Invest. 2020;130:1552–1564. PubMed PMC
Shan W, Ma X, Deng F. Is LukS-PV a novel experimental therapy for leukemia? Gene. 2017;600:44–47. PubMed
Christopher MJ, et al. Immune escape of relapsed AML cells after allogeneic transplantation. N. Engl. J. Med. 2018;379:2330–2341. PubMed PMC
Toffalori C, et al. Immune signature drives leukemia escape and relapse after hematopoietic cell transplantation. Nat. Med. 2019;25:603–611. PubMed
Muffly L, et al. Infusion of donor-derived CD8(+) memory T cells for relapse following allogeneic hematopoietic cell transplantation. Blood Adv. 2018;2:681–690. PubMed PMC
Lupianez CB, et al. Polymorphisms in host immunity-modulating genes and risk of invasive aspergillosis: results from the AspBIOmics Consortium. Infect. Immun. 2015;84:643–657. PubMed PMC
Manuel Sanchez-Maldonado J, et al. NFKB2 polymorphisms associate with the risk of developing rheumatoid arthritis and response to TNF inhibitors: Results from the REPAIR consortium. Sci. Rep. 2020;10:4316. PubMed PMC
Chattopadhyay S, et al. Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance. Leukemia. 2020;34:1187–1191. PubMed
Rios-Tamayo R, et al. A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis. Oncotarget. 2016;7:59029–59048. PubMed PMC
Nyholt DR. A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am. J. Hum. Genet. 2004;74:765–769. PubMed PMC
Li Y, et al. A functional genomics approach to understand variation in cytokine production in humans. Cell. 2016;167:1099–1110 e1014. PubMed
Schirmer M, et al. Linking the human gut microbiome to inflammatory cytokine production capacity. Cell. 2016;167:1897. PubMed
Ter Horst R, et al. Host and environmental factors influencing individual human cytokine responses. Cell. 2016;167:1111–1124 e1113. PubMed PMC
Moffatt MF, et al. A large-scale, consortium-based genomewide association study of asthma. N. Engl. J. Med. 2010;363:1211–1221. PubMed PMC
Pickrell JK, et al. Detection and interpretation of shared genetic influences on 42 human traits. Nat. Genet. 2016;48:709–717. PubMed PMC
Urayama KY, et al. Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups. J. Natl. Cancer Inst. 2012;104:240–253. PubMed PMC
Bruserud O, et al. Interleukin 1 receptor antagonist (IL1RA) in acute leukaemia: IL1RA is both secreted spontaneously by myelogenous leukaemia blasts and is a part of the acute phase reaction in patients with chemotherapy-induced leucopenia. Eur. J. Haematol. 1996;57:87–95. PubMed
Estrov Z, et al. Inhibition of acute myelogenous leukemia blast proliferation by interleukin-1 (IL-1) receptor antagonist and soluble IL-1 receptors. Blood. 1992;79:1938–1945. PubMed
Luz-Crawford P, et al. Mesenchymal stem cell-derived interleukin 1 receptor antagonist promotes macrophage polarization and inhibits B cell differentiation. Stem Cells. 2016;34:483–492. PubMed
Singh JK, Simoes BM, Howell SJ, Farnie G, Clarke RB. Recent advances reveal IL-8 signaling as a potential key to targeting breast cancer stem cells. Breast Cancer Res. 2013;15:210. PubMed PMC
Wang S, et al. CXCR2 macromolecular complex in pancreatic cancer: a potential therapeutic target in tumor growth. Transl. Oncol. 2013;6:216–225. PubMed PMC
Ning Y, et al. The CXCR2 antagonist, SCH-527123, shows antitumor activity and sensitizes cells to oxaliplatin in preclinical colon cancer models. Mol. Cancer Ther. 2012;11:1353–1364. PubMed
Jamieson T, et al. Inhibition of CXCR2 profoundly suppresses inflammation-driven and spontaneous tumorigenesis. J. Clin. Invest. 2012;122:3127–3144. PubMed PMC
Schinke C, et al. IL8-CXCR2 pathway inhibition as a therapeutic strategy against MDS and AML stem cells. Blood. 2015;125:3144–3152. PubMed PMC
Waugh DJ, Wilson C. The interleukin-8 pathway in cancer. Clin. Cancer Res. 2008;14:6735–6741. PubMed
Sharma B, Nawandar DM, Nannuru KC, Varney ML, Singh RK. Targeting CXCR2 enhances chemotherapeutic response, inhibits mammary tumor growth, angiogenesis, and lung metastasis. Mol. Cancer Ther. 2013;12:799–808. PubMed PMC
Lee YS, et al. Interleukin-8 and its receptor CXCR2 in the tumour microenvironment promote colon cancer growth, progression and metastasis. Br. J. Cancer. 2012;106:1833–1841. PubMed PMC
Onishi S, et al. Toll-like receptor 2-mediated interleukin-8 expression in gingival epithelial cells by the Tannerella forsythia leucine-rich repeat protein BspA. Infect. Immun. 2008;76:198–205. PubMed PMC
Oliveira-Nascimento L, Massari P, Wetzler LM. The role of TLR2 in infection and immunity. Front. Immunol. 2012;3:79. PubMed PMC
Sabroe I, et al. Selective roles for Toll-like receptor (TLR)2 and TLR4 in the regulation of neutrophil activation and life span. J. Immunol. 2003;170:5268–5275. PubMed
Ghosh TK, et al. Toll-like receptor (TLR) 2-9 agonists-induced cytokines and chemokines: I. Comparison with T cell receptor-induced responses. Cell Immunol. 2006;243:48–57. PubMed
Okamoto M, et al. Toll-like receptors (TLRs) are expressed by myeloid leukaemia cell lines, but fail to trigger differentiation in response to the respective TLR ligands. Br. J. Haematol. 2009;147:585–587. PubMed
Li K, et al. Targeting acute myeloid leukemia with a proapoptotic peptide conjugated to a Toll-like receptor 2-mediated cell-penetrating peptide. Int. J. Cancer. 2014;134:692–702. PubMed
Kuett A, et al. IL-8 as mediator in the microenvironment-leukaemia network in acute myeloid leukaemia. Sci. Rep. 2015;5:18411. PubMed PMC
Vijay V, et al. Interleukin-8 blockade prevents activated endothelial cell mediated proliferation and chemoresistance of acute myeloid leukemia. Leuk. Res. 2019;84:106180. PubMed PMC
Weidenaar AC, et al. High acute myeloid leukemia derived VEGFA levels are associated with a specific vascular morphology in the leukemic bone marrow. Cell Oncol. (Dordr) 2011;34:289–296. PubMed PMC
Aguayo A, et al. Angiogenesis in acute and chronic leukemias and myelodysplastic syndromes. Blood. 2000;96:2240–2245. PubMed
Kim DH, Lee NY, Lee MH, Sohn SK. Vascular endothelial growth factor gene polymorphisms may predict the risk of acute graft-versus-host disease following allogeneic transplantation: preventive effect of vascular endothelial growth factor gene on acute graft-versus-host disease. Biol. Blood Marrow Transplant. 2008;14:1408–1416. PubMed
Swertz MA, et al. The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button. BMC Bioinformatics. 2010;11(Suppl 12):S12. PubMed PMC
Wilkinson MD, et al. The FAIR Guiding Principles for scientific data management and stewardship. Sci. Data. 2016;3:160018. PubMed PMC
Westra HJ, et al. Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat. Genet. 2013;45:1238–1243. PubMed PMC