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遗传基因型与前列腺癌预后。

Inherited genotype and prostate cancer outcomes.

作者信息

Rebbeck Timothy R

机构信息

Department of Biostatistics and Epidemiology, Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6021, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2002 Oct;11(10 Pt 1):945-52.

Abstract

Prostate cancer is the most commonly diagnosed noncutaneous tumor in North American men and confers significant morbidity and mortality to the general population. The use of screening tools to detect prostate cancer at an early stage may have beneficial effects on an individual's prognosis. However, the intense use of these screening modalities also detects tumors that may have a relatively benign course and for which intensive treatment is not necessary. There is a large body of research that evaluated biochemical, physiological, or somatic genetic measures in relation to prostate cancer progression or prognosis. Environmental exposures may also affect these outcomes. In contrast, inherited markers of genetic susceptibility to prostate cancer have largely been used to predict occurrence of disease rather than disease outcome. The use of inherited genetic markers to evaluate prostate cancer outcome could enhance our ability to identify those men who are more likely to develop clinically significant prostate cancer and to intervene in these men to reduce morbidity and mortality resulting from prostate cancer.

摘要

前列腺癌是北美男性中最常被诊断出的非皮肤肿瘤,给普通人群带来了显著的发病率和死亡率。使用筛查工具在早期检测前列腺癌可能对个体的预后产生有益影响。然而,这些筛查方式的大量使用也会检测出一些可能具有相对良性病程且无需强化治疗的肿瘤。有大量研究评估了与前列腺癌进展或预后相关的生化、生理或体细胞遗传指标。环境暴露也可能影响这些结果。相比之下,前列腺癌遗传易感性的遗传标记在很大程度上一直被用于预测疾病的发生而非疾病的转归。使用遗传标记来评估前列腺癌的转归可以提高我们识别那些更有可能发展为具有临床意义的前列腺癌的男性的能力,并对这些男性进行干预,以降低前列腺癌导致的发病率和死亡率。

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