Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK.
Int J Mol Sci. 2019 Mar 19;20(6):1389. doi: 10.3390/ijms20061389.
Prostate cancer is the most commonly diagnosed malignancy in men, claiming over350,000 lives worldwide annually. Current diagnosis relies on prostate-specific antigen (PSA)testing, but this misses some aggressive tumours, and leads to the overtreatment of non-harmfuldisease. Hence, there is an urgent unmet clinical need to identify new diagnostic and prognosticbiomarkers. As prostate cancer is a heterogeneous and multifocal disease, it is likely that multiplebiomarkers will be needed to guide clinical decisions. Fluid-based biomarkers would be ideal, andattention is now turning to minimally invasive liquid biopsies, which enable the analysis oftumour components in patient blood or urine. Effective diagnostics using liquid biopsies willrequire a multifaceted approach, and a recent high-profile review discussed combining multipleanalytes, including changes to the tumour transcriptome, epigenome, proteome, and metabolome.However, the concentration on genomics-based paramaters for analysing liquid biopsies ispotentially missing a goldmine. Glycans have shown huge promise as disease biomarkers, anddata suggests that integrating biomarkers across multi-omic platforms (including changes to theglycome) can improve the stratification of patients with prostate cancer. A wide range ofalterations to glycans have been observed in prostate cancer, including changes to PSAglycosylation, increased sialylation and core fucosylation, increased O-GlcNacylation, theemergence of cryptic and branched N-glyans, and changes to galectins and proteoglycans. In thisreview, we discuss the huge potential to exploit glycans as diagnostic and prognostic biomarkersfor prostate cancer, and argue that the inclusion of glycans in a multi-analyte liquid biopsy test forprostate cancer will help maximise clinical utility.
前列腺癌是男性最常见的恶性肿瘤,全球每年有超过 35 万人因此死亡。目前的诊断依赖于前列腺特异性抗原(PSA)检测,但这种方法会漏掉一些侵袭性肿瘤,并导致对无害疾病的过度治疗。因此,临床上迫切需要识别新的诊断和预后生物标志物。由于前列腺癌是一种异质性和多灶性疾病,可能需要多种生物标志物来指导临床决策。基于液体的生物标志物将是理想的,目前人们的注意力转向微创的液体活检,它可以分析患者血液或尿液中的肿瘤成分。使用液体活检进行有效的诊断需要采用多方面的方法,最近的一份备受瞩目的综述讨论了结合多种分析物,包括肿瘤转录组、表观基因组、蛋白质组和代谢组的变化。然而,基于基因组参数的分析方法可能忽略了一个金矿。糖链作为疾病生物标志物具有巨大的潜力,数据表明,整合多组学平台上的生物标志物(包括糖组的变化)可以改善前列腺癌患者的分层。在前列腺癌中观察到广泛的糖链改变,包括 PSA 糖基化的改变、唾液酸化和核心岩藻糖基化增加、O-GlcNAc 酰化增加、隐蔽和分支 N-糖链的出现,以及凝集素和蛋白聚糖的改变。在这篇综述中,我们讨论了将糖链作为前列腺癌诊断和预后生物标志物的巨大潜力,并认为将糖链纳入前列腺癌的多分析物液体活检测试中,将有助于最大限度地提高临床实用性。