Nakagawa Masatoshi, Karashima Takashi, Kamada Masayuki, Yoshida Eisaku, Yoshimura Toru, Nojima Masanori, Inoue Keiji, Shuin Taro, Seiki Motoharu, Koshikawa Naohiko
Diagnostic Division, Abbott Japan Co. Ltd., Chiba, Japan.
Division of Cancer Cell Research, Kanagawa Cancer Center Research Institute, 2-3-2 Nakao, Yokohama, 241-8515 Japan.
Biomark Res. 2017 Oct 13;5:29. doi: 10.1186/s40364-017-0109-4. eCollection 2017.
Monomeric laminin-γ2 in urine is a potential biomarker for bladder cancer. However, the current detection system uses an antibody that cannot discriminate between monomeric laminin-γ2 and the heterotrimeric γ2 chain of laminin-332, which may cause false-positive reactions. The present study aimed to develop a fully automated chemiluminescence immunoassay system using a specific monoclonal antibody against monomeric laminin-γ2.
In total, 237 urine specimens (84 from patients with bladder cancer, 48 from patients with benign urological disease, and 105 from healthy donors) were collected, and monomeric laminin-γ2 values in the urine were measured using a fully automated chemiluminescence immunoassay.
The results revealed that laminin-γ2 values in patients with benign urological disease were comparable to those of healthy donors and that the chemiluminescence immunoassay's lower limit of detection was 10 pg/mL (approximately 20-fold better than the sandwich enzyme-linked immunosorbent assay's limit of 200 pg/mL). Moreover, the chemiluminescence immunoassay demonstrated that patients with bladder cancer, including non-muscle invasive bladder cancer (≤pT1), had higher laminin-γ2 values than patients with benign urological disease or healthy donors.
These results suggest that urine monomeric laminin-γ2 may be a promising biomarker to diagnose cases of non-muscle invasive bladder cancer using a fully automated chemiluminescence immunoassay system.
尿液中的单体层粘连蛋白γ2是膀胱癌的潜在生物标志物。然而,当前的检测系统使用的抗体无法区分单体层粘连蛋白γ2和层粘连蛋白332的异源三聚体γ2链,这可能会导致假阳性反应。本研究旨在开发一种使用针对单体层粘连蛋白γ2的特异性单克隆抗体的全自动化学发光免疫分析系统。
总共收集了237份尿液标本(84份来自膀胱癌患者,48份来自良性泌尿系统疾病患者,105份来自健康捐赠者),并使用全自动化学发光免疫分析法测量尿液中的单体层粘连蛋白γ2值。
结果显示,良性泌尿系统疾病患者的层粘连蛋白γ2值与健康捐赠者相当,化学发光免疫分析的检测下限为10 pg/mL(比夹心酶联免疫吸附测定法的200 pg/mL下限约好20倍)。此外,化学发光免疫分析表明,包括非肌层浸润性膀胱癌(≤pT1)在内的膀胱癌患者层粘连蛋白γ2值高于良性泌尿系统疾病患者或健康捐赠者。
这些结果表明,尿液单体层粘连蛋白γ2可能是一种有前景的生物标志物,可使用全自动化学发光免疫分析系统诊断非肌层浸润性膀胱癌病例。