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
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
相关论文
共 34 条
[1]  
Chhanabhai M, 1997, BLOOD, V90, P2451
[2]  
Donoghue S, 1999, CANCER RES, V59, P5386
[3]   Many cuts to ruin:: a comprehensive update of caspase substrates [J].
Fischer, U ;
Jänicke, RU ;
Schulze-Osthoff, K .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (01) :76-100
[4]  
Fujikawa K, 2000, ANTICANCER RES, V20, P1927
[5]   Evidence that apoptosis and terminal differentiation of epidermal keratinocytes are distinct processes [J].
Gandarillas, A ;
Goldsmith, LA ;
Gschmeissner, S ;
Leigh, IM ;
Watt, FM .
EXPERIMENTAL DERMATOLOGY, 1999, 8 (01) :71-79
[6]   Mitochondria and cell death [J].
Halestrap, AP ;
Doran, E ;
Gillespie, JP ;
O'Toole, A .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2000, 28 :170-177
[7]   Analysis of proliferation, apoptosis and keratin expression in cultured normal and immortalized human buccal keratinocytes [J].
Hansson, A ;
Bloor, BK ;
Sarang, Z ;
Haig, Y ;
Morgan, PR ;
Stark, HJ ;
Fusenig, NE ;
Ekstrand, J ;
Grafström, RC .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2003, 111 (01) :34-41
[8]   Prognostic significance of caspase-3 expression in primary resected esophageal squamous cell carcinoma [J].
Hsia, JY ;
Chen, CY ;
Chen, JT ;
Hsu, CP ;
Shai, SE ;
Yang, SS ;
Chuang, CY ;
Wang, PY ;
Miaw, J .
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2003, 29 (01) :44-48
[9]   Caspase-3 is required for DNA fragmentation and morphological changes associated with apoptosis [J].
Jänicke, RU ;
Sprengart, ML ;
Wati, MR ;
Porter, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9357-9360
[10]   Identity of TUNEL-positive cells in the oral buccal epithelium of normal mucosa and lichen lesions [J].
Karatsaidis, A ;
Schreurs, O ;
Axéll, T ;
Helgeland, K ;
Schenck, K .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2004, 33 (05) :264-268