Journal of International Oncology ›› 2020, Vol. 47 ›› Issue (9): 513-517.doi: 10.3760/cma.j.cn371439-20191223-00069

• Original Articles •     Next Articles

Serum proteomic-based analysis identifying autoantibody against ENO1 as a potential diagnostic biomarker in nasopharyngeal carcinoma

Zhan Xiaofen1, Weng Xuefen2, Yang Shihuang3, Xu Yiwei2, Peng Yuhui2, Guo Hong4()   

  1. 1Department of Pathology, Shantou Central Hospital of Guangdong Province, Shantou 515000, China
    2Department of Clinical Laboratory Medicine, Cancer Hospital of Shantou University Medical College, Shantou 515000, China
    3Department of Emergency, Second People's Hospital of Shantou Longhu District of Guangdong Province, Shantou 515000, China
    4Department of Radiation Oncology, Cancer Hospital of Shantou University Medical College, Shantou 515000, China
  • Received:2019-12-23 Revised:2020-03-11 Online:2020-09-08 Published:2020-10-27
  • Contact: Guo Hong E-mail:38469073@qq.com
  • Supported by:
    Natural Science Foundation of Guangdong Province(2018A030307079);Natural Science Foundation of Guangdong Province(2019A151501-1873);Shantou Science and Technology Planning Project(2017-119-18)

Abstract:

Objective To screen and identify autoantibody biomarker to diagnose patients with nasopharyngeal carcinoma (NPC). Methods Candidate autoantibodies against tumor-associated antigens were identified from NPC CNE2 cells using serological proteome analysis. Levels of candidate autoantibody biomarkers were measured by enzyme-linked immunosorbent assay (ELISA) in 50 patients with NPC and 80 normal controls recruited from the Cancer Hospital of Shantou University Medical College between July 2014 and January 2015. Receiver operating characteristic curve (ROC) was employed to evaluate diagnostic efficacy. Results Serological proteome analysis showed that sera from patients with NPC yielded a positive spot, of which was identified as enolase 1 (ENO1). ELISA results showed that the level of serum autoantibody against ENO1 in patients with NPC was significantly higher than that in normal controls [0.165 (0.088, 0.378) vs. 0.100 (0.054, 0.117), Z=4.077, P<0.001]. With the optimum diagnostic cutoff of 0.164, ROC curve showed the diagnostic sensitivity and specificity of autoantibodies against ENO1 were 52.0% and 90.0%, respectively. Measurement of autoantibody against ENO1 demonstrated a positive rate of 75.0% for early stage NPC. Conclusion Autoantibody against ENO1 may be a potential diagnostic biomarker for NPC.

Key words: Esophageal neoplasms, Early diagnosis, Autoantibody, Serological proteome analysis technique, Enolase 1