Institute of Cancer Research, Sutton, Surrey, UK.
Clin Oncol (R Coll Radiol). 2012 Oct;24(8):545-55. doi: 10.1016/j.clon.2012.05.001. Epub 2012 Jun 7.
Prostate-specific antigen is currently commonly used as a screening biomarker for prostate cancer, but it has limitations in both sensitivity and specificity. The development of novel biomarkers for early cancer detection has the potential to improve survival, reduce unnecessary investigations and benefit the health economy. Here we review the use and limitations of prostate-specific antigen and its subtypes, urinary biomarkers including PCA3, alpha-methylacyl-CoA racemase, the TMPRSS2-ERG fusion gene and microseminoprotein-beta, and other novel markers in both serum and urine. Many of these biomarkers are at early stages of development and require evaluation in prospective trials to determine their potential usefulness in clinical practice. Genetic profiling may allow for the targeting of high-risk populations for screening and may offer the opportunity to combine biomarker results with genotype to aid risk assessment.
前列腺特异性抗原(PSA)目前常用于前列腺癌的筛查生物标志物,但它在灵敏度和特异性方面均存在局限性。新型生物标志物的开发对于早期癌症检测具有改善生存率、减少不必要的检查和有益于卫生经济的潜力。在这里,我们回顾了 PSA 及其亚型、尿生物标志物(包括 PCA3、α-甲基酰基辅酶 A 消旋酶、TMPRSS2-ERG 融合基因和微 Seminoprotein-beta)以及血清和尿液中其他新型标志物的应用和局限性。其中许多生物标志物仍处于早期开发阶段,需要在前瞻性试验中进行评估,以确定它们在临床实践中的潜在用途。基因谱分析可以针对高危人群进行筛查,并提供将生物标志物结果与基因型相结合以辅助风险评估的机会。