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https://hdl.handle.net/1822/62280
Título: | Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients |
Autor(es): | Ziv, Elad Dean, Eric Hu, Donglei Martino, Alessandro Serie, Daniel Curtin, Karen Campa, Daniele Aftab, Blake Bracci, Paige Buda, Gabriele Zhao, Yi Caswell-Jin, Jennifer Diasio, Robert Dumontet, Charles Dudziński, Marek Fejerman, Laura Greenberg, Alexandra Huntsman, Scott Jamroziak, Krzysztof Jurczyszyn, Artur Kumar, Shaji Atanackovic, Djordje Glenn, Martha Cannon-Albright, Lisa A Jones, Brandt Lee, Adam Marques, Herlander Martin, Thomas Martinez-Lopez, Joaquin Rajkumar, Vincent Sainz, Juan Vangsted, Annette Juul Wątek, Marzena Wolf, Jeffrey Slager, Susan Camp, Nicola J Canzian, Federico Vachon, Celine |
Palavras-chave: | Genome-Wide Association Study Humans Kaplan-Meier Estimate Multiple Myeloma Polymorphism, Single Nucleotide Chromosomes, Human, Pair 16 |
Data: | 2015 |
Editora: | Nature Research |
Revista: | Nature Communications |
Citação: | Ziv, E., Dean, E., Hu, D. et al. Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients. Nat Commun 6, 7539 (2015) doi:10.1038/ncomms8539 |
Resumo(s): | Here we perform the first genome-wide association study (GWAS) of multiple myeloma (MM) survival. In a meta-analysis of 306 MM patients treated at UCSF and 239 patients treated at the Mayo clinic, we find a significant association between SNPs near the gene FOPNL on chromosome 16p13 and survival (rs72773978; P=6 × 10(-10)). Patients with the minor allele are at increased risk for mortality (HR: 2.65; 95% CI: 1.94-3.58) relative to patients homozygous for the major allele. We replicate the association in the IMMEnSE cohort including 772 patients, and a University of Utah cohort including 318 patients (rs72773978 P=0.044). Using publicly available data, we find that the minor allele was associated with increased expression of FOPNL and increased expression of FOPNL was associated with higher expression of centrosomal genes and with shorter survival. Polymorphisms at the FOPNL locus are associated with survival among MM patients. |
Tipo: | Artigo |
Descrição: | A corrigendum to this article was published on 09 December 2015: https://doi.org/10.1038/ncomms10203. The corrigendum is also available at: http://hdl.handle.net/1822/62281 |
URI: | https://hdl.handle.net/1822/62280 |
DOI: | 10.1038/ncomms8539 |
ISSN: | 2041-1723 |
e-ISSN: | 2041-1723 |
Arbitragem científica: | yes |
Acesso: | Acesso aberto |
Aparece nas coleções: | ICVS - Artigos em revistas internacionais / Papers in international journals |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
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ncomms8539.pdf | 703,42 kB | Adobe PDF | Ver/Abrir |