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Search for transmembrane protein in gastric cancer by the Escherichia coli ampicillin secretion trap: expression of DSC2 in gastric cancer with intestinal phenotype

Authors :
Naohide Oue
Masazumi Okajima
Naoya Sakamoto
Jonathan M. Graff
Tetsutaro Hayashi
Wataru Yasui
Kazuhiro Sentani
Tsuyoshi Noguchi
Katsuhiro Anami
Takao Hinoi
Source :
The Journal of Pathology. 221:275-284
Publication Year :
2010
Publisher :
Wiley, 2010.

Abstract

Gastric cancer (GC) is one of the most common malignancies worldwide. Genes expressed only in cancer tissue, and especially on the cell membrane, will be useful molecular markers for diagnosis and may also be good therapeutic targets. To identify genes that encode transmembrane proteins present in GC, we generated Escherichia coli ampicillin secretion trap (CAST) libraries from two GC cell lines and normal stomach. By sequencing 4320 colonies from CAST libraries, we identified 30 candidate genes that encode transmembrane proteins present in GC. Quantitative reverse transcription-polymerase chain reaction analysis of these candidates revealed that ZDHHC14, BST2, DRAM2, and DSC2 were expressed much more highly in GC than in 14 kinds of normal tissues. Among these, DSC2 encodes desmocollin 2, which is one of three known desmocollins. Immunohistochemical analysis demonstrated that 22 (28%) of 80 GC cases were positive for desmocollin 2, and desmocollin 2 expression was observed frequently in GC with the intestinal mucin phenotype. Furthermore, desmocollin 2 expression was correlated with CDX2 expression. These results suggest that expression of desmocollin 2, induced by CDX2, may be a key regulator for GC with the intestinal mucin phenotype. Our results provide a list of genes that have high potential as a diagnostic and therapeutic target for GC. Copyright © 2010 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Details

ISSN :
00223417
Volume :
221
Database :
OpenAIRE
Journal :
The Journal of Pathology
Accession number :
edsair.doi.dedup.....526c4465b4d52ed6cd68350956be53f7
Full Text :
https://doi.org/10.1002/path.2717