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Original Research

Open Access

Serum expression level of cytokine and chemokine correlates with progression of human ovarian cancer

  • J.H. Luo1,2
  • C.Y. Zhang2
  • C.Y. Lu3
  • G.H. Guo1
  • Y.P. Tian2
  • Y.L. Li1,*,

1Department of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, China

2Department of Clinical Biochemistry, Chinese PLA General Hospital, Beijing, China

3Department of Gynecology and Obstetrics, Chinese PLA 254 Hospital, Tianjin, China

DOI: 10.12892/ejgo3207.2017 Vol.38,Issue 1,February 2017 pp.33-39

Published: 10 February 2017

*Corresponding Author(s): Y.L. Li E-mail: liyali30115@163.com

Abstract

Objective: This work was designed to determine the relationship between serum expression level of cytokines and chemokines and progression of human ovarian cancer, and to evaluate the utility and diagnostic value of target markers as risk indicators. Materials and Methods: A set of candidate cytokines and chemokines (GM-CSF, IFN-γ, GRO, IL-1β, IL-2, IL-6, IL-8, MCP-1, TNF-α, VEGF, EGF, RANTES, CCL21/6Ckine, and SDF-1/CXCL12) were measured using Luminex liquid chip technique in healthy women (n=75) and in women with ovarian cancer (n=77). Results: EGF, IL-6, MCP-1, 6Ckine, RANTES, and IL-10 were significantly overexpressed in the tumor group compared to those in normal controls, while IL-2 was reduced. The combined markers (EGF, MCP-1, 6Ckine, IL-6, and TNF-α) achieved 91.1% sensitivity, 65.8% specificity, and 83.3% area under the ROC curve (AUC) in distinguishing serous ovarian cancer from health controls. Conclusion: This study suggested that serum expression level of cytokines and chemokines correlate with progression of human ovarian cancer. The association of EGF, MCP-1, 6Ckine, IL-6, and TNF-α may contribute to increase diagnosis rate of malignant ovarian tumors.

Keywords

Cytokine; Chemokine; Serum; Ovarian cancer detection.

Cite and Share

J.H. Luo,C.Y. Zhang,C.Y. Lu,G.H. Guo,Y.P. Tian,Y.L. Li. Serum expression level of cytokine and chemokine correlates with progression of human ovarian cancer. European Journal of Gynaecological Oncology. 2017. 38(1);33-39.

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