Expression of serum MIP-3α and cystatin A in patients with nasopharyngeal carcinoma and their clinical significance
10.3969/j.issn.1007-3969.2013.10.011
- VernacularTitle:鼻咽癌患者血清MIP-3α与cystatin A表达及其临床意义
- Author:
Jun LI
;
Minzhong TANG
;
Aiying LU
;
Weiming ZHONG
;
Jianquan GAO
;
Yuming ZHENG
;
Hong ZENG
;
Wansheng CHEN
;
Wei LIANG
;
Yonglin CAI
- Publication Type:Journal Article
- Keywords:
Nasopharyngeal carcinoma;
Macrophage inflammatory protein-3α;
Cystatin A;
Clinical outcome
- From:
China Oncology
2013;(10):845-851
- CountryChina
- Language:Chinese
-
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-3αand 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-3αand cystatin A were 92.1%and 42.1%, respectively;and the specificity of MIP-3αand 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-3αand cystatin A in pre-treatment patients with NPC were higher than those in post-treatment patients and controls. Serum MIP-3αand cystatin A levels were associated with overall stage of NPC, and MIP-3αwas also associated with T classification of NPC. The serum MIP-3αlevel 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-3αand 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-3αand cystatin A may contribute to the NPC staging and prediction of short-term clinical outcomes.
