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      GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21

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          Abstract

          Childhood acute lymphoblastic leukemia (ALL) (age 0–14 years) is 20% more common in Latino Americans than non-Latino whites. We conduct a genome-wide association study in a large sample of 3263 Californian children with ALL (including 1949 of Latino heritage) and 3506 controls matched on month and year of birth, sex, and ethnicity, and an additional 12,471 controls from the Kaiser Resource for Genetic Epidemiology Research on Aging Cohort. Replication of the strongest genetic associations is performed in two independent datasets from the Children’s Oncology Group and the California Childhood Leukemia Study. Here we identify new risk loci on 17q12 near IKZF3/ZPBP2/GSDMB/ORMDL3, a locus encompassing a transcription factor important for lymphocyte development ( IKZF3), and at an 8q24 region known for structural contacts with the MYC oncogene. These new risk loci may impact gene expression via local (four 17q12 genes) or long-range (8q24) interactions, affecting function of well-characterized hematopoietic and growth-regulation pathways.

          Abstract

          Childhood acute lymphoblastic leukemia is common in Latino Americans. Here, the authors conduct a genome-wide association study in a Californian cohort containing children of Latino heritage, and identify loci on 17q12 and 8q24 which may affect hematopoietic and growth-regulation pathways.

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          Most cited references24

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          Genome-wide association identifies multiple ulcerative colitis susceptibility loci.

          Ulcerative colitis is a chronic, relapsing inflammatory condition of the gastrointestinal tract with a complex genetic and environmental etiology. In an effort to identify genetic variation underlying ulcerative colitis risk, we present two distinct genome-wide association studies of ulcerative colitis and their joint analysis with a previously published scan, comprising, in aggregate, 2,693 individuals with ulcerative colitis and 6,791 control subjects. Fifty-nine SNPs from 14 independent loci attained an association significance of P < 10(-5). Seven of these loci exceeded genome-wide significance (P < 5 x 10(-8)). After testing an independent cohort of 2,009 cases of ulcerative colitis and 1,580 controls, we identified 13 loci that were significantly associated with ulcerative colitis (P < 5 x 10(-8)), including the immunoglobulin receptor gene FCGR2A, 5p15, 2p16 and ORMDL3 (orosomucoid1-like 3). We confirmed association with 14 previously identified ulcerative colitis susceptibility loci, and an analysis of acknowledged Crohn's disease loci showed that roughly half of the known Crohn's disease associations are shared with ulcerative colitis. These data implicate approximately 30 loci in ulcerative colitis, thereby providing insight into disease pathogenesis.
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            Recent Insights into the Molecular Mechanisms Underlying Pyroptosis and Gasdermin Family Functions.

            Pyroptosis is an inflammatory form of cell death that not only protects multicellular organisms from invading pathogenic bacteria and microbial infections, but can also lead to sepsis and lethal septic shock if overactivated. Here, we present an overview of recent developments within the pyroptosis field, beginning with the discovery of Gasdermin D (GSDMD) as a substrate of caspase-1 and caspase-11 upon detection of cytosolic lipopolysaccharide (LPS). Cleavage releases the N-terminal domain of GSDMD, causing it to form cytotoxic pores in the plasma membrane of cells. We further discuss the implications for the rest of the gasdermin (GSDM) family, which are emerging as mediators of programmed cell death in a variety of processes that regulate cellular differentiation and proliferation.
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              Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.

              A genome-wide association screen for primary biliary cirrhosis risk alleles was performed in an Italian cohort. The results from the Italian cohort replicated IL12A and IL12RB associations, and a combined meta-analysis using a Canadian dataset identified newly associated loci at SPIB (P = 7.9 x 10(-11), odds ratio (OR) = 1.46), IRF5-TNPO3 (P = 2.8 x 10(-10), OR = 1.63) and 17q12-21 (P = 1.7 x 10(-10), OR = 1.38).
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                Author and article information

                Contributors
                joe.wiemels@ucsf.edu
                xiaomei.ma@yale.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                18 January 2018
                18 January 2018
                2018
                : 9
                : 286
                Affiliations
                [1 ]ISNI 0000 0001 2297 6811, GRID grid.266102.1, Department of Epidemiology and Biostatistics, , University of California San Francisco, ; 1450 3rd Street, San Francisco, CA 94158 USA
                [2 ]ISNI 0000 0001 2297 6811, GRID grid.266102.1, Department of Neurological Surgery, , University of California San Francisco, ; 1450 3rd Street, San Francisco, CA 94158 USA
                [3 ]ISNI 0000 0001 2297 6811, GRID grid.266102.1, Institute for Human Genetics, , University of California San Francisco, ; 1450 3rd Street, San Francisco, CA 94158 USA
                [4 ]ISNI 0000 0001 2156 6853, GRID grid.42505.36, Department of Preventative Medicine, , University of Southern California, ; SSB 318D 2001 N. Soto Street, Los Angeles, CA 90033 USA
                [5 ]ISNI 0000 0001 2181 7878, GRID grid.47840.3f, School of Public Health, , University of California Berkeley, ; 1950 University Avenue, Suite 460, Berkeley, CA 94720 USA
                [6 ]ISNI 0000 0004 1936 914X, GRID grid.266818.3, Department of Epidemiology, School of Community Health Sciences, , University of Nevada Reno, ; 1664 N. Virginia Street, Reno, NV 89557 USA
                [7 ]ISNI 0000000419368710, GRID grid.47100.32, Department of Chronic Diseases Epidemiology, School of Public Health, , Yale University, ; 60 College Street, New Haven, CT 06520 USA
                [8 ]ISNI 0000 0001 2188 0957, GRID grid.410445.0, University of Hawaii Cancer Center, ; 701 Ilalo Street, Honolulu, HI 96813 USA
                Author information
                http://orcid.org/0000-0001-5484-9016
                http://orcid.org/0000-0003-3950-4815
                Article
                2596
                10.1038/s41467-017-02596-9
                5773513
                29348612
                10cac79c-5278-436f-8eb9-79cc6b2abbb7
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 June 2017
                : 13 December 2017
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