Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Epidemiology, Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Proteomics Clin Appl. 2016 Nov;10(11):1113-1121. doi: 10.1002/prca.201600074. Epub 2016 Sep 20.
The aim of this pilot study was to conduct a nontargeted exploratory proteomics profiling analysis on sera obtained from patients diagnosed with diffuse large B-cell lymphoma (DLBCL) with the goal of identifying disease-specific biomarkers.
Sera from 87 participants (57 chemotherapy-naïve diffuse DLBCL patients, 30 controls frequency-matched by age group and World Health Organization (WHO) BMI categories) that were part of a large San Francisco Bay Area case-control study of non-Hodgkin lymphoma were analyzed by liquid chromatography combined with tandem mass spectrometry.
Thirty-five proteins (p-adjusted <0.05) were identified as differentially abundant between the DLBCL patients at various disease stages as compared to the controls. Of these, five proteins were randomly selected for further confirmation by ELISA: adiponectin (AdipoQ), cluster of differentiation 14 (CD14), heparin sulfate proteoglycan core protein (HSPG2), extracellular matrix 1 (ECM1), and alpha-1-antichymotrypsin (ACT). These proteins were statistically significantly elevated by 68.8, 37.0, 61.6, 68.0, and 32.0%, respectively, in DLBCL patient sera as compared to controls.
These preliminary data when combined with other cancer-related data regarding these proteins warrant continued research in clinical and large prospective studies to clarify the role for these biomarkers in DLBCL pathogenesis and/or prognosis.
本初步研究旨在对诊断为弥漫性大 B 细胞淋巴瘤 (DLBCL) 的患者的血清进行非靶向探索性蛋白质组学分析,以鉴定疾病特异性生物标志物。
本研究分析了来自 87 名参与者(57 名未经化疗的弥漫性 DLBCL 患者,30 名按年龄组和世界卫生组织 (WHO) BMI 类别匹配的对照组)的血清,这些参与者是旧金山湾区大型非霍奇金淋巴瘤病例对照研究的一部分,采用液相色谱-串联质谱联用技术进行分析。
与对照组相比,35 种蛋白质(调整后的 p 值 <0.05)在不同疾病阶段的 DLBCL 患者中差异丰富。其中,有 5 种蛋白质通过 ELISA 进一步随机验证:脂联素 (AdipoQ)、分化簇 14 (CD14)、硫酸乙酰肝素蛋白多糖核心蛋白 (HSPG2)、细胞外基质 1 (ECM1) 和α-1-抗胰蛋白酶 (ACT)。与对照组相比,这些蛋白质在 DLBCL 患者血清中的含量分别升高了 68.8%、37.0%、61.6%、68.0%和 32.0%。
当这些初步数据与其他有关这些蛋白质的癌症相关数据相结合时,需要在临床和大型前瞻性研究中进一步研究这些生物标志物在 DLBCL 发病机制和/或预后中的作用。