Shi Tujin, Quek Sue-Ing, Gao Yuqian, Nicora Carrie D, Nie Song, Fillmore Thomas L, Liu Tao, Rodland Karin D, Smith Richard D, Leach Robin J, Thompson Ian M, Vitello Elizabeth A, Ellis William J, Liu Alvin Y, Qian Wei-Jun
Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Department of Urology, University of Washington, Seattle, WA, USA.
Oncotarget. 2017 Oct 9;8(60):101887-101898. doi: 10.18632/oncotarget.21710. eCollection 2017 Nov 24.
Biomarkers for effective early diagnosis and prognosis of prostate cancer are still lacking. Multiplexed assays for cancer-associated proteins could be useful for identifying biomarkers for cancer detection and stratification. Herein, we report the development of sensitive targeted mass spectrometry assays for simultaneous quantification of 10 prostate cancer-associated proteins in urine. The diagnostic utility of these markers was evaluated with an initial cohort of 20 clinical urine samples. Individual marker concentration was normalized against the measured urinary prostate-specific antigen level as a reference of prostate-specific secretion. The areas under the receiver-operating characteristic curves for the 10 proteins ranged from 0.75 for CXL14 to 0.87 for CEAM5. Furthermore, MMP9 level was found to be significantly higher in patients with high Gleason scores, suggesting a potential of MMP9 as a marker for risk level assessment. Taken together, our work illustrated the feasibility of accurate multiplexed measurements of low-abundance cancer-associated proteins in urine and provided a viable path forward for preclinical verification of candidate biomarkers for prostate cancer.
目前仍缺乏用于前列腺癌有效早期诊断和预后评估的生物标志物。针对癌症相关蛋白的多重检测方法可能有助于识别用于癌症检测和分层的生物标志物。在此,我们报告了用于同时定量尿液中10种前列腺癌相关蛋白的灵敏靶向质谱检测方法的开发。使用20份临床尿液样本的初始队列评估了这些标志物的诊断效用。将各个标志物的浓度相对于测得的尿前列腺特异性抗原水平进行标准化,以此作为前列腺特异性分泌的参考。这10种蛋白质的受试者工作特征曲线下面积范围从CXL14的0.75到CEAM5的0.87。此外,发现MMP9水平在高Gleason评分患者中显著更高,这表明MMP9有作为风险水平评估标志物的潜力。综上所述,我们的工作说明了准确多重测量尿液中低丰度癌症相关蛋白的可行性,并为前列腺癌候选生物标志物的临床前验证提供了一条可行的途径。