Rowe Dianna J, Khalil Timothy A, Kammer Michael N, Godfrey Caroline M, Zou Yong, Vnencak-Jones Cindy L, Xiao David, Deppen Stephen, Grogan Eric L
Department of Medicine, Division of Allergy, Pulmonary and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Biosens Bioelectron X. 2025 May;23. doi: 10.1016/j.biosx.2025.100593. Epub 2025 Feb 17.
Studies show CYFRA 21-1 fragments of cytokeratin 19 (CK19) to be promising biomarkers for non-small cell lung cancer (NSCLC). Although previous literature identifies specific CYFRA 21-1 antibody binding epitopes, the exact molecular weight of the CK19 fragment being detected by current assays is not well-documented. Serum samples from 58 patients (lung cancer (N = 36), control (N = 22)) were used to measure CYFRA 21-1 across four different quantification assays: enzyme-linked immunosorbent assay (ELISA), chemiluminescent assay (ChLIA), electrochemiluminescence immunoassay (ECLIA), and compensated interferometric reader (CIR). In the cancer group, correlation between ECLIA and ELISA was high (R = 0.948, r = 0.868) while correlation between ECLIA vs ChLIA and ECLIA vs CIR was low (R= 0.005, r = -0.0593), (R = 0.0275, r = 0.167), respectively. In the control group, correlation between ECLIA and ELISA was high (R = 0.861, r = 0.927) while correlation between ECLIA vs ChLIA and ECLIA vs CIR was low (R = 0.0079, r = -0.0593), (R = 0.0244, r = -0.102), respectively. Compared to ECLIA, concordance coefficients ( ) were poor ( < 0.90) across all assays except for cancers group in ELISA ( = 0.913). ECLIA was the only assay to report control ranges above 1 ng/mL CYFRA 21-1 (ECLIA, 1.14-21.59 ng/mL; ELISA, 0.79-24.26 ng/mL; ChLIA, 0.062-0.691 ng/mL; 0.08-7.68 ng/mL). Differing sizes of the protein being measured by each assay may have a role in the discrepancies observed. Given the different CYFRA 21-1 concentration estimates among assays, further characterization of the fragment and its release during epithelial malignancies, such as NSCLC, is imperative to developing effective biomarker assays.
研究表明,细胞角蛋白19(CK19)的细胞角蛋白片段抗原21-1(CYFRA 21-1)是有前景的非小细胞肺癌(NSCLC)生物标志物。尽管先前的文献确定了CYFRA 21-1抗体结合表位,但目前检测方法所检测的CK19片段的确切分子量尚无充分文献记载。来自58例患者(肺癌(N = 36),对照(N = 22))的血清样本用于通过四种不同的定量检测方法测量CYFRA 21-1:酶联免疫吸附测定(ELISA)、化学发光测定(ChLIA)、电化学发光免疫测定(ECLIA)和补偿干涉仪读数器(CIR)。在癌症组中,ECLIA与ELISA之间的相关性较高(R = 0.948,r = 0.868),而ECLIA与ChLIA之间以及ECLIA与CIR之间的相关性较低(分别为R = 0.005,r = -0.0593),(R = 0.0275,r = 0.167)。在对照组中,ECLIA与ELISA之间的相关性较高(R = 0.861,r = 0.927),而ECLIA与ChLIA之间以及ECLIA与CIR之间的相关性较低(分别为R = 0.0079,r = -0.0593),(R = 0.0244,r = -0.102)。与ECLIA相比,除癌症组的ELISA(κ = 0.913)外,所有检测方法的一致性系数(κ)均较差(κ < 0.90)。ECLIA是唯一报告CYFRA 21-1对照范围高于1 ng/mL的检测方法(ECLIA,1.14 - 21.59 ng/mL;ELISA,0.79 - 24.26 ng/mL;ChLIA,0.062 - 0.691 ng/mL;0.08 - 7.68 ng/mL)。每种检测方法所测量的蛋白质大小不同可能是观察到差异的原因之一。鉴于各检测方法对CYFRA 21-1浓度的估计不同,进一步表征该片段及其在诸如NSCLC等上皮恶性肿瘤期间的释放情况对于开发有效的生物标志物检测方法至关重要。