Caspase-3 expression is reduced, in the absence of cleavage, in terminally differentiated normal oral epithelium but is increased in oral squamous cell carcinomas and correlates with tumour stage

被引:33
|
作者
Hague, A
Eveson, JW
MacFarlane, M
Huntley, S
Janghra, N
Thavaraj, S
机构
[1] Univ Bristol, Dept Oral & Dent Sci, Sch Dent, Bristol BS1 2LY, Avon, England
[2] Univ Leicester, MRC, Toxicol Unit, Leicester LE1 9HN, Leics, England
来源
JOURNAL OF PATHOLOGY | 2004年 / 204卷 / 02期
关键词
caspase-3; apoptosis; terminal differentiation; oral epithelium; oral carcinoma;
D O I
10.1002/path.1630
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oral carcinomas are known to have a greater apoptotic index than normal oral epithelium, study, these morphologically evident as shrinking cells with condensed chromatin. In this apoptotic cells stained positively for cleaved (active) caspase-3. In normal oral epithelium, cleaved caspase-3 positive-cells were only rarely detected. The terminally differentiated surface epithelial layers did not express cleaved caspase-3. The caspase-3 pro-enzyme showed a gradient of expression in normal oral epithelium, decreasing with differentiation. No expression was detectable in surface epithelial layers. Lack of expression of the major 'executioner' caspase-3 may, at least in part, explain differences in morphology between terminally differentiated and apoptotic cells. In cancers of different tissue origins, caspase-3 pro-enzyme expression can be either increased or decreased compared with normal tissue counterparts. To determine how caspase-3 expression alters during oral carcinogenesis, caspase-3 expression was compared in 39 samples of normal oral epithelium and 54 oral squamous cell carcinomas. Squamous cell carcinomas had more intense caspase-3 staining than normal epithelium (p < 0.001). Moreover, within the oral squamous cell carcinoma series, there was significantly more intense nuclear and cytoplasmic staining with increasing STNMP stage (p = 0.017 and 0.03, respectively). This was a reflection of significant associations with site (S), palpable lymph nodes (N), and differentiation (P). Both caspase-3 staining intensity and the percentage of cells positive for caspase-3 were inversely associated with differentiation. Studies of the mechanisms by which high levels of caspase-3 expression are tolerated in oral carcinoma cells may identify targets that can be used to harness caspase-3 overexpression for therapeutic benefit. Copyright (C) 2004 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:175 / 182
页数:8
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