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‘Senescence‐associated’ β‐galactosidase activity in the upper gastrointestinal tract
Author(s) -
Going James J.,
Stuart Robert C.,
Downie Martin,
FletcherMonaghan Aileen J.,
Nicol Keith W.
Publication year - 2002
Publication title -
the journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.964
H-Index - 184
eISSN - 1096-9896
pISSN - 0022-3417
DOI - 10.1002/path.1059
Subject(s) - intestinal metaplasia , adenocarcinoma , stomach , dysplasia , pathology , epithelium , metaplasia , senescence , gastroenterology , medicine , gastrointestinal tract , intraepithelial neoplasia , staining , in vivo , cancer , esophagus , biology , prostate , microbiology and biotechnology
β‐galactosidase activity at pH 6 is associated in vitro with senescence and cellular death, but in vivo data are sparse. This study undertook firstly to map ‘senescence‐associated’ β‐galactosidase activity (SAβG) at pH 6 in normal epithelia and mucosae of the upper gastrointestinal tract. As escape from senescence confers a proliferative advantage, a reduction in SAβG activity might be predicted in neoplasia and their precursors in vivo . This prediction was tested in metaplastic, dysplastic, and neoplastic epithelium of the upper gastrointestinal tract. Histochemical staining for SAβG was performed at pH 6 on cryostat sections of 350 endoscopic biopsies from sites including oesophagus, stomach, and duodenum of 46 patients: 28 with Barrett's oesophagus (two with adenocarcinoma), 15 with gastric adenocarcinoma, and three with oesophageal squamous cancer. A staining score (range 0–6) was assigned to epithelial cells in all mucosae and scores were calculated for surface (luminal), intermediate, and deep (basal) layers. The strongest SAβG activity was in surface luminal cells of normal duodenal mucosa (mean score 3.6±0.5; n =19), ‘specialized’ Barrett's mucosa (mean 2.2±0.12; n =105), and intestinal metaplasia in the stomach (mean 2.4±0.40; n =16). Squamous epithelium was consistently negative for SAβG activity. Low‐ and high‐grade Barrett's dysplasia showed no decrease in SAβG activity, but reduced activity was seen in gastric and oesophageal adenocarcinomas (mean 1.24±0.29; n =17; p =0.012). In six gastric adenocarcinomas, there was no detectable activity. Whether SAβG is truly a marker of cellular senescence in vivo remains to be determined. Activity is low in mucosal proliferation compartments and increases with cellular differentiation, especially in native or metaplastic intestinal mucosae. SAβG activity persists in dysplastic mucosae but may show some reduction or loss in adenocarcinomas ( p =0.0012). Loss of SAβG activity is not, therefore, an early event in glandular dysplasia–neoplasia of the upper gastrointestinal tract. Copyright © 2002 John Wiley & Sons, Ltd.