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PMID: 8049082 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Biliary glycoprotein mRNA expression is increased in primary lung cancer, especially in squamous cell carcinoma.

American journal of respiratory cell and molecular biology ·Vol. 11 ·No. 2 ·1994-08-00 ·Pages 214-20

Ohwada A, Takahashi H, Nagaoka I, Kira S

Abstract

Biliary glycoprotein (BGP), a member of the carcinoembryonic antigen gene family, is a cell surface glycoprotein that has both a transmembrane domain and a cytoplasmic domain. BGPs consist of at least four isoforms (BGPa, b, c, and d) and function in vitro as Ca(2+)-dependent homotypic intercellular adhesion molecules. The mRNA expression of BGP gene was investigated in specimens of primary and metastatic cancer tissues from 15 patients with primary lung cancer (six squamous cell carcinomas, five adenocarcinomas, and four small cell carcinomas). The specimens were also compared with normal adjacent tissues of the same individuals with squamous cell carcinoma. BGP mRNA expression was increased in carcinomatous tissues of the primary site, especially in squamous cell carcinoma, but was not detected in adjacent normal tissues by Northern blot analysis or in situ hybridization. Interestingly, BGP mRNA expression was apparently decreased in metastatic lesions compared with the primary site in the six individuals with squamous cell carcinoma. Furthermore, a loss of BGPa isoform was observed by reverse transcriptase-polymerase chain reaction in four of six patients with squamous cell carcinoma. These results suggest that the reduction of BGP expression may play an important role in the process of metastasis through decreasing adhesive interactions with surrounding cells, especially in squamous cell carcinoma.

MeSH Terms
Adenocarcinoma/metabolism,pathology Antigens, CD Base Sequence Blotting, Northern Carcinoma, Small Cell/metabolism,pathology Carcinoma, Squamous Cell/metabolism,pathology,secondary Cell Adhesion Molecules DNA Primers Gene Expression Glycoproteins/biosynthesis Humans In Situ Hybridization Kidney/metabolism Liver/metabolism Lung/metabolism,pathology Lung Neoplasms/metabolism,pathology Molecular Sequence Data Neoplasm Metastasis Polymerase Chain Reaction RNA, Messenger/biosynthesis RNA, Neoplasm/analysis,biosynthesis Transcription, Genetic
Chemicals
Antigens, CD CD66 antigens Cell Adhesion Molecules DNA Primers Glycoproteins RNA, Messenger RNA, Neoplasm
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ohwada A
Department of Respiratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Takahashi H
Nagaoka I
Kira S
Article Info
Journal
American journal of respiratory cell and molecular biology
Abbr.
Am J Respir Cell Mol Biol
ISSN
1044-1549
Published
1994-08-00
Pages
214-20
Language
English
Region
United States
NLM ID
8917225
Subset
IM
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