Polygenic risk score for genetic evaluation of prostate cancer risk in Asian populations: A narrative review
Decreasing costs of genetic testing and interest in disease inheritance has changed the landscape of cancer prediction in prostate cancer (PCa), and guidelines now include genetic testing for high-risk groups. Familial and hereditary PCa comprises approximately 20% and 5% of all PCa, respectively. M...
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Published in | Investigative and clinical urology Vol. 62; no. 3; pp. 256 - 266 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
The Korean Urological Association
01.05.2021
Korean Urological Association 대한비뇨의학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2466-0493 2466-054X 2466-054X |
DOI | 10.4111/icu.20210124 |
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Summary: | Decreasing costs of genetic testing and interest in disease inheritance has changed the landscape of cancer prediction in prostate cancer (PCa), and guidelines now include genetic testing for high-risk groups. Familial and hereditary PCa comprises approximately 20% and 5% of all PCa, respectively. Multifaceted disorders like PCa are caused by a combinatory effect of rare genes of high penetrance and smaller genetic variants of relatively lower effect size. Polygenic risk score (PRS) is a novel tool utilizing PCa-associated single nucleotide polymorphisms (SNPs) identified from genome-wide association study (GWAS) to generate an additive estimate of an individual's lifetime genetic risk for cancer. However, most PRS are developed based on GWAS collected from mainly European populations and do not address ethnic differences in PCa genetics. This review highlights the attempts to generate a PRS tailored to Asian males including data from Korea, China, and Japan, and discuss the clinical implications for prediction of early onset and aggressive PCa. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 https://www.icurology.org/pdf/10.4111/icu.20210124 |
ISSN: | 2466-0493 2466-054X 2466-054X |
DOI: | 10.4111/icu.20210124 |