Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility

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作者
Pik Fang Kho
Xuemin Wang
Gabriel Cuéllar-Partida
Thilo Dörk
Ellen L. Goode
Diether Lambrechts
Rodney J. Scott
Amanda B. Spurdle
Tracy A. O’Mara
Dylan M. Glubb
机构
[1] QIMR Berghofer Medical Research Institute,Department of Genetics and Computational Biology
[2] Queensland University of Technology,School of Biomedical Sciences
[3] 23andMe Inc,Gynaecology Research Unit
[4] Hannover Medical School,Department of Health Science Research
[5] Division of Epidemiology,Laboratory for Translational Genetics, Department of Human Genetics
[6] Mayo Clinic,Division of Molecular Medicine
[7] KU Leuven,Discipline of Medical Genetics, School of Biomedical Sciences and Pharmacy, Faculty of Health
[8] VIB Center for Cancer Biology,undefined
[9] Pathology North,undefined
[10] John Hunter Hospital,undefined
[11] University of Newcastle,undefined
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摘要
Genome-wide association studies (GWAS) have revealed sixteen risk loci for endoemtrial cancer but the identification of candidate susceptibility genes remains challenging. Here, we perform transcriptome-wide association study (TWAS) analyses using the largest endometrial cancer GWAS and gene expression from six relevant tissues, prioritizing eight candidate endometrial cancer susceptibility genes, one of which (EEFSEC) is located at a potentially novel endometrial cancer risk locus. We also show evidence of biologically relevant tissue-specific expression associations for CYP19A1 (adipose), HEY2 (ovary) and SKAP1 (whole blood). A phenome-wide association study demonstrates associations of candidate susceptibility genes with anthropometric, cardiovascular, diabetes, bone health and sex hormone traits that are related to endometrial cancer risk factors. Lastly, analysis of TWAS data highlights candidate compounds for endometrial cancer repurposing. In summary, this study reveals endometrial cancer susceptibility genes, including those with evidence of tissue specificity, providing insights into endometrial cancer aetiology and avenues for therapeutic development.
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