Cancer Research Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
Genes (Basel). 2024 Jul 18;15(7):939. doi: 10.3390/genes15070939.
Genome-wide association studies (GWAS) have accelerated the exploration of genotype-phenotype associations, facilitating the discovery of replicable genetic markers associated with specific traits or complex diseases. This narrative review explores the statistical methodologies developed using GWAS data to investigate relationships between various phenotypes, focusing on endometrial cancer, the most prevalent gynecological malignancy in developed nations. Advancements in analytical techniques such as genetic correlation, colocalization, cross-trait locus identification, and causal inference analyses have enabled deeper exploration of associations between different phenotypes, enhancing statistical power to uncover novel genetic risk regions. These analyses have unveiled shared genetic associations between endometrial cancer and many phenotypes, enabling identification of novel endometrial cancer risk loci and furthering our understanding of risk factors and biological processes underlying this disease. The current status of research in endometrial cancer is robust; however, this review demonstrates that further opportunities exist in statistical genetics that hold promise for advancing the understanding of endometrial cancer and other complex diseases.
全基因组关联研究(GWAS)加速了基因型-表型关联的探索,有助于发现与特定特征或复杂疾病相关的可重复遗传标记。本叙述性评论探讨了使用 GWAS 数据研究各种表型之间关系的统计方法,重点关注发达国家最常见的妇科恶性肿瘤——子宫内膜癌。遗传相关分析、共定位分析、跨表型基因座识别分析和因果推断分析等分析技术的进步,使我们能够更深入地研究不同表型之间的关联,提高发现新遗传风险区域的统计能力。这些分析揭示了子宫内膜癌与许多表型之间的共同遗传关联,确定了新的子宫内膜癌风险基因座,并进一步加深了我们对这种疾病的风险因素和生物学过程的理解。目前子宫内膜癌的研究现状非常强劲;然而,本综述表明,统计遗传学中还有进一步的机会,有望提高对子宫内膜癌和其他复杂疾病的认识。