China Oncology ›› 2013, Vol. 23 ›› Issue (10): 845-851.doi: 10.3969/j.issn.1007-3969.2013.10.011

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Expression of serum MIP-3α and cystatin A in patients with nasopharyngeal carcinoma and their clinical significance

LI Jun1,2,TANG Min-zhong1,3,LU Ai-ying1,2,ZHONG Wei-ming4,GAO Jian-quan4,ZHENG Yu-ming1,ZENG Hong1,CHEN Wan-sheng4,LIANG Wei4,CAI Yong-lin1,2   

  1. 1.Wuzhou Health System Key Laboratory for Nasopharyngeal Carcinoma Etiology and Molecular Mechanism, Wuzhou Guangxi 543002, China;
    2.Clinical Laboratory, Wuzhou Red Cross Hospital, Wuzhou Guangxi 543002, China;
    3.College of Life Science and Bio-Engineering, Beijing University of Technology, Beijing 100022, China; 
    4.Department of Oncology, Wuzhou Red Cross Hospital, Wuzhou Guangxi 543002, China
  • Online:2013-10-25 Published:2014-02-19
  • Contact: CAI Yong-lin E-mail: cylzen@163.com

Abstract:

Background and purpose: To date, it mainly depended on imaging examination for detection of residual lesions, recurrence and distant metastasis, evaluation the sensitivity of radiotherapy and chemotherapy, and prognosis in nasopharyngeal carcinoma (NPC). Thus, searching for new tumor markers for NPC early diagnosis and individualized treatment is still merited. This study was aimed to investigate the expressions of serum macrophage inflammatory protein (MIP)-3α and cystatin A in patients with NPC before and after treatment, and to explore two markers value in NPC diagnosis, clinicopathological characteristics and clinical outcome assessment. Methods: The serum levels of MIP-3α and cystatin A in 140 primary NPC patients without distant metastasis before and after treatment were detected by enzyme-linked immunosorbent assay (ELISA) and compared with those in 100 healthy controls. Results: The sensitivity of MIP-3α and cystatin A were 92.1% and 42.1%, respectively; and the specificity of MIP-3α and cystatin A were 86.0% and 85.0%, respectively. All 140 NPC patients had complete remission (CR) or partial remission (PR). Serum levels of MIP-3α and cystatin A in pre-treatment patients with NPC were higher than those in post-treatment patients and controls. Serum MIP-3α and cystatin A levels were associated with overall stage of NPC, and MIP-3α was also associated with T classification of NPC. The serum MIP-3α level in NPC with CR after treatment reduced to the level in control group, and that was still significantly higher in NPC with PR than in control group. No significant difference was found in the serum cystatin A level between NPC with CR or PR after treatment and control group. During 1-year follow-up, the post-treatment serum levels of MIP-3α and cystatin A were significantly higher in patients with distant metastasis than in patients without distant metastasis and controls. There was found statistically significant correlation between MIP-3α and cystatin A.Conclusion: MIP-3α may be a potential marker of NPC serological diagnosis. The detection of serum MIP-3α and cystatin A may contribute to the NPC staging and prediction of short-term clinical outcomes.

Key words: Nasopharyngeal carcinoma, Macrophage inflammatory protein-3α, Cystatin A, Clinical outcome