Apoptotic cell death and its relationship to gastric carcinogenesis

被引:6
|
作者
Bir, Ferda [1 ]
Calli-Demirkan, Nese
Tufan, A. Cevilk
Akbulut, Metin
Satiroglu-Tufan, N. Lale
机构
[1] Pamukkale Univ, Sch Med, Dept Pathol, TR-20070 Denizli, Turkey
[2] Pamukkale Univ, Sch Med, Dept Histol & Embryol, Denizli, Turkey
[3] Pamukkale Univ, Sch Med, Dept Med Biol, Ctr Genet Diag,Mol Genet Lab, Denizli, Turkey
关键词
p53; bax; bcl-2; TUNEL staining; intestinal metaplasia; apoptosis; gastric cancer;
D O I
10.3748/wjg.v13.i23.3183
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the apoptotic process of cells within the intestinal metaplasia areas co-localizing with chronic gastritis and gastric carcinomas and to analyze the involvement of proteins regulating apoptosis in the process of intestinal metaplasia related gastric carcinogenesis. METHODS: Forty-two gastric carcinoma and seventeen chronic gastritis cases were included in this study. All cases were examined for the existence of intestinal metaplasia. Ten cases randomly selected from each group were processed for TUNEL assay. TUNEL positive cells within the intestinal metaplasia areas, colocalizing either to gastric carcinoma or chronic gastritis, were counted and converted to apoptotic indices. In addition, p53, bcl-2 and bax expression patterns within these tissues were analyzed on the basis of immunohistochemistry. RESULTS: Twenty-eight of the cases were intestinal and 14 of the cases were diffuse type adenocarcinomas. 64% (27/42) of the gastric carcinoma cases had intestinal metaplasia. Intestinal metaplasia co-localized more with intestinal type carcinomas compared with diffuse type carcinomas [75% (21/28) v5 42% (6/14), respectively; P <= 0.05]. The mean apoptotic index in tumor cells was 0.70 +/- 0.08. The mean apoptotic index in intestinal metaplasias co-localizing to tumors was significantly higher than that of intestinal metaplasias co-localizing to chronic gastritis (0.70 +/- 0.03 vs 0.09 +/- 0.01, respectively; P <= 0.05). p53 positivity was not observed in areas of intestinal metaplasia adjacent to tumors or chronic gastritis. Intestinal metaplasia areas adjacent to tumors showed lower cytoplasmic bcl-2 Positivity compared to intestinal metaplasia areas adjacent to chronic gastritis [55.5% (15/27) vs 70.5% (12/17), respectively]. On the other hand, intestinal metaplasia areas adjacent to tumors showed significantly higher cytoplasmic bax positivity compared to intestinal metaplasia areas adjacent to chronic gastritis [44.4% (12/27) v5 11.7% (2/17), respectively; P <= 0.05]. CONCLUSION: Existence of apoptotic cells on the basis of TUNEL positivity is shown in intestinal metaplasias co-localizing to both diffuse and intestinal type gastric cancers in this study. Our results also suggested bax expression dependent induction of apoptosis especially in intestinal metaplasia areas adjacent to tumors. These findings strongly support the involvement of apoptotic mechanisms in the process of gastric carcinogenesis especially in the transition from intestinal metaplasia to gastric cancer. It may be suggested that induction of apoptosis in intestinal metaplasia areas adjacent to tumors may involve different mechanisms than induction by chronic inflammation. (C) 2007 The WJG Press. All rights reserved.
引用
收藏
页码:3183 / 3188
页数:6
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