{"title":"[甘聚糖靶向前列腺癌生物标志物的开发与临床应用]。","authors":"Chikara Ohyama, Tohru Yoneyama, Yuki Tobisawa, Tomokazu Ishikawa, Shingo Hatakeyama, Takuya Koie, Kazuyuki Mori","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Prostate cancer (PCa) is now the most common male malignant tumor in both Japan and Western countries. Prostate-specific antigen (PSA) has been widely used for the early detection of PCa; however, it is not an ideal biomarker due to its low specificity. Aberrant glycosylation is closely associated with malignant transformation and cancer progression. Recent advances in glycobiology techniques can be applied to the development of novel biomarkers for PCa. We previously identified PCa-associated aberrant glycosylation on PSA, that is, α2,3-linked sialylation as an additional terminal N-glycan on free PSA(S2,3PSA). We then developed a new assay system for the measurement of S2,3PSA utilizing the μTAS method. The area under the curve (AUC) for the detection of PCa with the %S2,3PSA ratio was significantly better than that with total PSA. Another urgent issue in clinical practice for PCa is the over-treatment of patients with a low malignant potential, as aggressive treatment is not necessary. To overcome this problem, it is essential to develop a useful tool for the measurement of the malignant potential. Core2 ,β-1,6-N-acetylglucosaminyltransferase-1 (GCNT1, C2GnT) is a key enzyme that forms core 2-branched 0-glycans. Its expression is associated with the progression of several cancers. We established a mouse IgG monoclonal antibody (mAb) against GCNT1 and examined the relationship of GCNT1 expression with the clinicopathological status of PCa. GCNT1- negative patients were associated with significantly better PSA-free survival compared with GCNT1-positive patients. Furthermore, we established new methods for GCNT1 detection using urine samples of PCa patients. Immunoblotting was used to examine post-digital rectal examination (DRE) urine from PCa patients. Over 90% of GCNT1-positive PCa patients with high concentrations of serum PSA showed extracapsular extension in prostatectomy specimens. In conclusion, the clinical application of glycobiology techniques is a promising approach to develop novel biomarkers for PCa.</p>","PeriodicalId":21457,"journal":{"name":"Rinsho byori. 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引用次数: 0
摘要
前列腺癌(PCa)是目前日本和西方国家最常见的男性恶性肿瘤。前列腺特异性抗原(PSA)已被广泛用于前列腺癌的早期检测;然而,由于特异性较低,它并不是一种理想的生物标志物。异常糖基化与恶性转化和癌症进展密切相关。糖生物学技术的最新进展可以应用于PCa的新型生物标志物的开发。我们之前发现了PSA上与ca相关的异常糖基化,即游离PSA上的α2,3-链唾液酰化作为附加的末端n -聚糖(S2,3PSA)。然后,我们利用μTAS法建立了一种新的测定S2,3PSA的检测系统。曲线下面积(AUC)用%S2,3PSA比检测PCa明显优于总PSA。前列腺癌临床实践中的另一个紧迫问题是对低恶性潜能患者的过度治疗,因为没有必要进行积极治疗。为了克服这个问题,必须开发一种有用的工具来测量恶性潜能。Core2,β-1,6- n -乙酰氨基葡萄糖转移酶-1 (GCNT1, C2GnT)是形成核心2支0聚糖的关键酶。它的表达与几种癌症的进展有关。我们建立了抗GCNT1的小鼠IgG单克隆抗体(mAb),并检测了GCNT1表达与PCa临床病理状态的关系。与GCNT1阳性患者相比,GCNT1阴性患者的无psa生存率显著提高。此外,我们建立了使用PCa患者尿液样本检测GCNT1的新方法。采用免疫印迹法检测前列腺癌患者直肠指检后尿液。超过90%的血清PSA浓度高的gcnt1阳性PCa患者在前列腺切除术标本中表现为囊外延伸。总之,糖生物学技术的临床应用是开发前列腺癌新生物标志物的一种很有前景的方法。
[Development and Clinical Application of Glycan-Targeted Biomarkers for Prostate Cancer].
Prostate cancer (PCa) is now the most common male malignant tumor in both Japan and Western countries. Prostate-specific antigen (PSA) has been widely used for the early detection of PCa; however, it is not an ideal biomarker due to its low specificity. Aberrant glycosylation is closely associated with malignant transformation and cancer progression. Recent advances in glycobiology techniques can be applied to the development of novel biomarkers for PCa. We previously identified PCa-associated aberrant glycosylation on PSA, that is, α2,3-linked sialylation as an additional terminal N-glycan on free PSA(S2,3PSA). We then developed a new assay system for the measurement of S2,3PSA utilizing the μTAS method. The area under the curve (AUC) for the detection of PCa with the %S2,3PSA ratio was significantly better than that with total PSA. Another urgent issue in clinical practice for PCa is the over-treatment of patients with a low malignant potential, as aggressive treatment is not necessary. To overcome this problem, it is essential to develop a useful tool for the measurement of the malignant potential. Core2 ,β-1,6-N-acetylglucosaminyltransferase-1 (GCNT1, C2GnT) is a key enzyme that forms core 2-branched 0-glycans. Its expression is associated with the progression of several cancers. We established a mouse IgG monoclonal antibody (mAb) against GCNT1 and examined the relationship of GCNT1 expression with the clinicopathological status of PCa. GCNT1- negative patients were associated with significantly better PSA-free survival compared with GCNT1-positive patients. Furthermore, we established new methods for GCNT1 detection using urine samples of PCa patients. Immunoblotting was used to examine post-digital rectal examination (DRE) urine from PCa patients. Over 90% of GCNT1-positive PCa patients with high concentrations of serum PSA showed extracapsular extension in prostatectomy specimens. In conclusion, the clinical application of glycobiology techniques is a promising approach to develop novel biomarkers for PCa.