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前列腺癌精准肿瘤学的基因组学中的种族差异。

Racial disparity in the genomics of precision oncology of prostate cancer.

机构信息

Division of Hematology and Oncology, Department of Medicine, University of California, San Francisco, California, USA.

Division of Hematology and Oncology, Department of Medicine, San Francisco Veterans Affairs Medical Center, San Francisco, California, USA.

出版信息

Cancer Rep (Hoboken). 2023 Sep;6 Suppl 1(Suppl 1):e1867. doi: 10.1002/cnr2.1867. Epub 2023 Aug 10.

Abstract

BACKGROUND

Significant racial disparities in prostate cancer incidence and mortality have been reported between African American Men (AAM), who are at increased risk for prostate cancer, and European American Men (EAM). In most of the studies carried out on prostate cancer, this population is underrepresented. With the advancement of genome-wide association studies, several genetic predictor models of prostate cancer risk have been elaborated, as well as numerous studies that identify both germline and somatic mutations with clinical utility.

RECENT FINDINGS

Despite significant advances, the AAM population continues to be underrepresented in genomic studies, which can limit generalizability and potentially widen disparities. Here we outline racial disparities in currently available genomic applications that are used to estimate the risk of individuals developing prostate cancer and to identify personalized oncology treatment strategies. While the incidence and mortality of prostate cancer are different between AAM and EAM, samples from AAM remain to be unrepresented in different studies.

CONCLUSION

This disparity impacts the available genomic data on prostate cancer. As a result, the disparity can limit the predictive utility of the genomic applications and may lead to the widening of the existing disparities. More studies with substantially higher recruitment and engagement of African American patients are necessary to overcome this disparity.

摘要

背景

非裔美国男性(AAM)患前列腺癌的风险增加,其前列腺癌发病率和死亡率与欧洲裔美国男性(EAM)存在显著差异。在大多数关于前列腺癌的研究中,这一人群代表性不足。随着全基因组关联研究的进展,已经制定了一些前列腺癌风险的遗传预测模型,以及许多具有临床应用价值的鉴定种系和体细胞突变的研究。

最新发现

尽管取得了重大进展,但 AAM 人群在基因组研究中仍然代表性不足,这可能限制其普遍性,并可能扩大差异。在这里,我们概述了目前用于估计个体患前列腺癌风险和确定个体化肿瘤治疗策略的基因组应用中的种族差异。虽然 AAM 和 EAM 之间的前列腺癌发病率和死亡率不同,但不同研究中 AAM 的样本仍然代表性不足。

结论

这种差异影响了前列腺癌的可用基因组数据。因此,这种差异可能会限制基因组应用的预测效用,并可能导致现有差异的扩大。需要进行更多的研究,以大幅提高招募和参与非洲裔美国患者的比例,以克服这种差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60e6/10440844/697b4da1a68f/CNR2-6-e1867-g001.jpg

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