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Expression of trefoil peptides (TFF1, TFF2, and TFF3) in gastric carcinomas, intestinal metaplasia, and non‐neoplastic gastric tissues
Author(s) -
Leung Wai K.,
Yu Jun,
Chan Francis K. L.,
To Ka F.,
Chan Michael W. Y.,
Ebert M. P. A.,
Ng Enders K. W.,
Sydney Chung S. C.,
Malfertheiner Peter,
Sung Joseph J. Y.
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.1147
Subject(s) - cancer , carcinogenesis , intestinal metaplasia , immunohistochemistry , pathology , biology , mucin , ectopic expression , cancer cell , cancer research , medicine , cell culture , genetics
Abstract Trefoil factor family (TFF) domain peptides consist of three members that play a role in intestinal mucosal defence and repair, and in tumourigenesis. The role of the three TFF members in the gastric carcinogenesis cascade remains poorly defined. This study examined seven gastric cell lines, 50 gastric cancers and their adjacent non‐cancer tissues, and tissues from 40 non‐cancer patients, in order to elucidate the chronology of TFF expression in various stages of gastric carcinogenesis. TFF expression was determined by RT‐PCR, immunohistochemistry, and western blot. Aberrant expression of TFF1, TFF2, and TFF3 was frequently detected in gastric cell lines. Specifically, TFF1 was detected in all non‐cancer patients, but was detected in only 50% of gastric cancer and 66% of adjacent normal tissues. TFF2 expression was demonstrated in 87.5% of non‐cancer patients, 34% of gastric carcinomas, and 58% of adjacent non‐cancer tissues. There was a significant correlation between TFF1 and TFF2 expression in gastric cancer and adjacent non‐cancer tissues ( p <0.001). By contrast, TFF3 was detected in 25% of non‐cancer patients and showed a predilection for areas with intestinal metaplasia ( p =0.005). Sixty‐two per cent of gastric cancers and 24% of neighbouring non‐cancer tissues showed TFF3 expression. Immunoreactivity against TFF3 was demonstrated in goblet cells of intestinal metaplasia and within the cytoplasm and nuclei of tumour cells. Progressive loss of TFF1 and TFF2, together with the induction of TFF3, is likely to be involved in the early stage of the multi‐step gastric carcinogenesis pathway. Copyright © 2002 John Wiley & Sons, Ltd.