Expression of glutathione s-transferase π in benign mucosa, Barrett's metaplasia, and adenocarcinoma of the esophagus

被引:14
|
作者
Chandra, RK
Bentz, BG
Haines, GK
Robinson, AM
Radosevich, JA
机构
[1] Northwestern Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Chicago, IL 60611 USA
[2] Northwestern Univ, Sch Med, Dept Pathol, Chicago, IL 60611 USA
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2002年 / 24卷 / 06期
关键词
glutathione s-transferase; esophagus; adenocarcinoma; metaplasia; immunohistochemistry;
D O I
10.1002/hed.10093
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. Glutathione s-transferase pi (GSTTI) is an enzyme that provides cellular protection against redox-mediated damage by free radicals, which have been implicated in carcinogenesis. Methods. Forty-three consecutive specimens from 19 patients were reviewed to identify samples of squamous mucosa, Barrett's metaplasia, adenocarcinoma, and peritumoral inflammation. Serial sections were stained with an anti-GSTpi polyclonal antibody, and GSTpi expression was quantified for each histologic group. Results. GSTpi expression was diminished in peritumoral mononuclear inflammatory cells (p < .001) compared with squamous epithelium, Barrett's metaplasia, or adenocarcinoma. Barrett's metaplasia exhibited decreased GSTpi expression compared with squamous mucosa (p = .045). GSTpi expression by >50% of adenocarcinoma cells was associated with an increased risk (2.25x) of disease at last follow-up. Conclusions. GSTpi is prominently expressed in esophageal squamous mucosa and adenocarcinoma. Mononuclear cells may be susceptible to oxidative damage secondary to weak GSTpi production. GSTpi may protect the tumor cells themselves from the cytotoxic effects of free radicals. The biochemical role of GSTpi expression in malignant transformation deserves further investigation. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:575 / 581
页数:7
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