Salivary glutathrone and uric acid levels in patients with head and neck squamous cell carcinoma

被引:48
作者
Almadori, Giovanni [1 ]
Bussu, Francesco
Galli, Jacopo
Limongelli, Attilio
Persichilli, Silvia
Zappacosta, Bruno
Minucci, Angelo
Paludetti, Gaetano
Giardina, Bruno
机构
[1] Univ Cattolica Sacro Cuore, Inst Otolaryngol, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Inst Clin Biochem, Rome, Italy
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2007年 / 29卷 / 07期
关键词
head and neck; oxidative damage; chemoprevention; salivary antioxidant system;
D O I
10.1002/hed.20579
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background, We evaluated the concentrations of glutathione and uric acid, low molecular weight antioxicants, in saliva of patients with head and neck squamous cell carcinoma (HNSCC), in order to identify differences with normal subjects and to obtain information about biochemical alterations of human saliva during carcinogenesis. Methods. We compared 50 HNSCC patients, divided in 2 subsets on the basis of tumor site, with a control group of 77 subjects, without a previous diagnosis of HNSCC, matched for age, sex, alcohol consumption, and smoking status. Results. At tests for equality of means by Welch and Brown-Forsythe, differences between groups resulted probable for salivary levels of glutathione (p =-.004 and p <.001 respectively) but not for salivary levels of uric acid (p =.228 and p =.122 respectively). Comparing groups by Tamhane test, the patients with oral or pharyngeal cancer had significantly higher salivary levels of glutathione than both controls and patients with laryngeal cancer. Conclusions. Salivary glutathione levels may be an index of oxidative stress at the level of the upper airways and in particular of oral cavity and pharynx. Therefore, high salivary glutathione may be an epidemiological marker to identify subjects with an increased risk of developing HNSCC, to submit to strict follow-up and chemoprevention. Metabolic alterations of saliva could be both an epidemiological marker and a target for chemoprevention of oral and oropharyngeal carcinogenesis. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:648 / 654
页数:7
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