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首页> 外文期刊>Scientific reports. >Serum N-glycan profiling is a potential biomarker for castration-resistant prostate cancer
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Serum N-glycan profiling is a potential biomarker for castration-resistant prostate cancer

机译:血清N-聚糖分析是用于抵抗阉割前列腺癌的潜在生物标志物

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摘要

We investigated the diagnostic and prognostic potential of serum N-glycan profiling for castration-resistant prostate cancer (CRPC). We retrospectively investigated serum N-glycan structural analysis by glycoblotting for 287 patients with benign prostatic hyperplasia (BPH), 289 patients with newly diagnosed prostate cancer (PC), 57 patients with PC treated with androgen-deprivation therapy without disease progression (PC-ADT), and 60 patients with CRPC. N-Glycan profiling was compared between the non-CRPC (BPH, newly diagnosed PC and PC-ADT) and CRPC patients. We obtained the quantitative score for CRPC (CRPC N-glycan score) by discriminant analysis based on the combination of 9 N-glycans that were significantly associated with CRPC. The median CRPC N-glycan score was found to be significantly greater in CRPC patients than in non-CRPC patients. The CRPC N-glycan score could classify CRPC patients with sensitivity, specificity, and area under the curve of 87%, 69%, and 0.88, respectively. The CRPC N-glycan score 1.7 points was significantly associated with poor prognosis in patients with CRPC. The glycoprotein analysis showed that not immunoglobulins but α-1-acid glycoprotein (AGP) were a potential candidate for the carrier protein of N-glycans. The overexpression of specific N-glycans may be associated with their castration-resistant status and be a potential biomarker for CRPC.
机译:我们研究了血清N-聚糖分析的诊断和预后潜力,用于抵抗抗阉割前列腺癌(CRPC)。我们回顾性地研究了GlycoBlotting的血清血清血清N-聚糖结构分析287例良性前列腺增生(BPH),289例新诊断的前列腺癌(PC),57例PC治疗雄激素剥夺治疗没有疾病进展的患者(PC-ADT )和60例CRPC患者。在非CRPC(BPH,新诊断的PC和PC-ADT)和CRPC患者之间比较了N-聚糖分析。通过基于9 n-Glycans的组合,获得了CRPC(CRPC N-Glycan评分)的定量评分,其与CRPC显着相关的9个N-聚糖。在CRPC患者中发现中位CRPC N-Glycan评分比非CRPC患者在CRPC患者中明显更大。 CRPC N-Glycan评分可以分别将CRPC患者分别分别为87%,69%和0.88的曲线下的敏感性,特异性和面积。 CRPC N-Glycan评分> 1.7点与CRPC患者的预后不良有显着相关。糖蛋白分析表明,不是免疫球蛋白,但α-1-酸糖蛋白(AGP)是N-聚乙烯载体的潜在候选者。特异性N-聚糖的过度表达可以与其抗阉割状态相关,并且是用于CRPC的潜在生物标志物。

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