International Journal of Cancer · 2021 · 12 citations · 22 references
Life SciencesGeneticsMolecular GeneticsGene ExpressionGene Expression AnalysisGenomicsClinical GenomicsExpression Quantitative Trait Loci AnalysisMultiple MyelomaQuantitative Trait AnalysisQuantitative Trait LociQuantitative Trait Loci MappingCell-type-specific Expression Quantitative Trait LociDisease Stage AssessmentExpression Quantitative Trait LociExpression Quantitative Trait Loci MappingExpression Quantitative Trait Locus AnalysisExpression Quantitative Trait Locus DiscoveryQuantitative Trait Loci (Qtl) MappingSingle-nucleotide Polymorphisms
Abstract Gene expression profiling can be used for predicting survival in multiple myeloma (MM) and identifying patients who will benefit from particular types of therapy. Some germline single nucleotide polymorphisms (SNPs) act as expression quantitative trait loci (eQTLs) showing strong associations with gene expression levels. We performed an association study to test whether eQTLs of genes reported to be associated with prognosis of MM patients are directly associated with measures of adverse outcome. Using the genotype‐tissue expression portal, we identified a total of 16 candidate genes with at least one eQTL SNP associated with their expression with P < 10 −7 either in EBV‐transformed B‐lymphocytes or whole blood. We genotyped the resulting 22 SNPs in 1327 MM cases from the International Multiple Myeloma rESEarch (IMMEnSE) consortium and examined their association with overall survival (OS) and progression‐free survival (PFS), adjusting for age, sex, country of origin and disease stage. Three polymorphisms in two genes ( TBRG4 ‐rs1992292, TBRG4 ‐rs2287535 and ENTPD1 ‐rs2153913) showed associations with OS at P < .05, with the former two also associated with PFS. The associations of two polymorphisms in TBRG4 with OS were replicated in 1277 MM cases from the International Lymphoma Epidemiology (InterLymph) Consortium. A meta‐analysis of the data from IMMEnSE and InterLymph (2579 cases) showed that TBRG4 ‐rs1992292 is associated with OS (hazard ratio = 1.14, 95% confidence interval 1.04‐1.26, P = .007). In conclusion, we found biologically a plausible association between a SNP in TBRG4 and OS of MM patients.
22
The Genotype-Tissue Expression (GTEx) project.
Annotation of functional variation in personal genomes using RegulomeDB
Alan P. Boyle, Eurie L. Hong, Manoj Hariharan et al. · Genome Research · 2012 · 2.9K citations · Full text
Reference-based phasing using the Haplotype Reference Consortium panel
Po‐Ru Loh, Petr Danecek, Pier Francesco Palamara et al. · Nature Genetics · 2016 · 2K citations · Full text
Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS
Dan L. Nicolae, Eric R. Gamazon, Wei Zhang et al. · PLoS Genetics · 2010 · 1.4K citations · Full text