Rapid Communication
Copyright ©2008 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. Feb 7, 2008; 14(5): 758-763
Published online Feb 7, 2008. doi: 10.3748/wjg.14.758
LINE-1 family member GCRG123 gene is up-regulated in human gastric signet-ring cell carcinoma
Gang-Shi Wang, Meng-Wei Wang, Ben-Yan Wu, Xin-Yan Yang, Wei-Hua Wang, Wei-Di You
Gang-Shi Wang, Meng-Wei Wang, Ben-Yan Wu, Xin-Yan Yang, Wei-Hua Wang, Wei-Di You, Department of Gerontal Gastroenterology, General Hospital of Chinese PLA, Beijing 100853, China
Correspondence to: Dr. Gang-Shi Wang, Department of Gerontal Gastroenterology, General Hospital of Chinese PLA, Beijing 100853, China. wanggangshi@hotmail.com
Telephone: +86-10-66937393
Fax: +86-10-66937393
Received: August 2, 2007
Revised: October 9, 2007
Published online: February 7, 2008
Abstract

AIM: To analyze the expression profiles of a human gastric-cancer-related gene, GCRG123, in human gastric signet-ring cell carcinoma tissues, and to perform bioinformatics analysis on GCRG123.

METHODS: In situ hybridization was used to explore the GCRG123 expression pattern in paraffin-embedded gastric tissues, including 15 cases of signet-ring cell carcinoma, 15 of intestinal-type adenocarcinoma, and 15 of normal gastric mucosa. Northern blotting was used to analyze the differences in GCRG123 expression between stomach signet-ring cell carcinoma and intestinal-type adenocarcinoma tissues. Online software, including BLAST, Multalin and BLAT, were applied for bioinformatics analysis. National Center for Biotechnology Information (NCBI) and the University of California Santa Cruz (UCSC) databases were used for the analyses.

RESULTS: The in situ hybridization signal appeared as blue precipitates restricted to the cytoplasm. Ten out of 15 cases of gastric signet ring cell carcinoma, normal gastric mucosal epithelium and pyloric glands showed high GCRG123 expression. Low GCRG123 expression was observed in gastric intestinal-type adenocarcinoma and normal gastric glands. Northern blotting revealed that GCRG123 was up-regulated in signet-ring cell carcinoma tissue but down-regulated in intestinal-type adenocarcinoma tissue. BLAST and Multalin analyses revealed that the GCRG123 sequence had 92% similarity with the ORF2 sequence of human long interspersed nuclear element retrotransposons (LINE-1, L1). BLAT analysis indicated that GCRG123 mapped to all chromosomes. GCRG123 was found to integrate in the intron-17 and -23 of Rb, 5’ flanking region of IL-2 and clotting factor IX genes.

CONCLUSION: GCRG123, an active member of the L1 family, was up-regulated in human gastric signet-ring cell carcinoma.

Keywords: Stomach; Signet-ring cell carcinoma; GCRG123; LINE-1; In situ hybridization; Bioinformatics