| Title: | Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting |
| Journal: | Journal of Translational Medicine |
| Published: | 5 Sep 2022 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/36064556/ |
| DOI: | https://doi.org/10.1186/s12967-022-03613-2 |
| URL: | https://translational-medicine.biomedcentral.com/counter/pdf/10.1186/s12967-022-03613-2 |
Publication 9825
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Abstract
BackgroundThe role of germline genetic factors in determining survival from cutaneous melanoma (CM) is not well understood.ObjectiveTo perform a genome-wide association study (GWAS) meta-analysis of melanoma-specific survival (MSS), and test whether a CM-susceptibility polygenic risk score (PRS) is associated with MSS.MethodsWe conducted two Cox proportional-hazard GWAS of MSS using data from the Melanoma Institute Australia, a high ultraviolet (UV) radiation setting (MIA; 5,762 patients with melanoma; 800 melanoma deaths) and UK Biobank (UKB: 5,220 patients with melanoma; 241 melanoma deaths), and combined them in a fixed-effects meta-analysis. Significant (P < 5 × 10-8) results were investigated in the Leeds Melanoma Cohort (LMC; 1,947 patients with melanoma; 370 melanoma deaths). We also developed a CM-susceptibility PRS using a large independent GWAS meta-analysis (23,913 cases, 342,870 controls). The PRS was tested for an association with MSS in the MIA and UKB cohorts.ResultsTwo loci were significantly associated with MSS in the meta-analysis of MIA and UKB with lead SNPs rs41309643 (G allele frequency 1.6%, HR = 2.09, 95%CI = 1.61-2.71, P = 2.08 × 10-8) on chromosome 1, and rs75682113 (C allele frequency 1.8%, HR = 2.38, 95%CI = 1.77-3.21, P = 1.07 × 10-8) on chromosome 7. While neither SNP replicated in the LMC, rs75682113 was significantly associated in the combined discovery and replication sets. After adjusting for age at diagnosis, sex and the first ten principal components, a one standard deviation increase in the CM-susceptibility PRS was associated with improved MSS in the discovery meta-analysis (HR = 0.88, 95% CI = 0.83-0.94, P = 6.93 × 10-5; I2 = 88%). However, this was only driven by the high UV setting cohort (MIA HR = 0.84, 95% CI = 0.78-0.90).ConclusionWe found two loci potentially associated with MSS. Increased genetic susceptibility to develop CM is associated with improved MSS in a high UV setting.</p>
19 Authors
- Mathias Seviiri
- Richard A. Scolyer
- D. Timothy Bishop
- Julia A. Newton-Bishop
- Mark M. Iles
- Serigne N. Lo
- Johnathan R. Stretch
- Robyn P. M. Saw
- Omgo E. Nieweg
- Kerwin F. Shannon
- Andrew J. Spillane
- Scott D. Gordon
- Catherine M. Olsen
- David C. Whiteman
- Maria Teresa Landi
- John F. Thompson
- Georgina V. Long
- Stuart MacGregor
- Matthew H. Law
1 Application
| Application ID | Title |
|---|---|
| 25331 | Gene mapping and genetic correlation across complex traits |
Enabling scientific discoveries that improve human health