help button home button
AJRCMB
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ohwada, A.
Right arrow Articles by Kira, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ohwada, A.
Right arrow Articles by Kira, S.

Am. J. Respir. Cell Mol. Biol., Vol 11, No. 2, 08 1994, 214-220.

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

A Ohwada, H Takahashi, I Nagaoka and S Kira
Department of Respiratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.

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.


This article has been cited by other articles:


Home page
CarcinogenesisHome page
A.-M. Bamberger, J. Briese, J. Gotze, I. Erdmann, H. M. Schulte, C. Wagener, and P. Nollau
Stimulation of CEACAM1 expression by 12-O-tetradecanoylphorbol-13-acetate (TPA) and calcium ionophore A23187 in endometrial carcinoma cells
Carcinogenesis, March 1, 2006; 27(3): 483 - 490.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
A. Ebrahimnejad, T. Streichert, P. Nollau, A. K. Horst, C. Wagener, A.-M. Bamberger, and J. Brummer
CEACAM1 Enhances Invasion and Migration of Melanocytic and Melanoma Cells
Am. J. Pathol., November 1, 2004; 165(5): 1781 - 1787.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. Kirshner, D. Schumann, and J. E. Shively
CEACAM1, a Cell-Cell Adhesion Molecule, Directly Associates with Annexin II in a Three-dimensional Model of Mammary Morphogenesis
J. Biol. Chem., December 12, 2003; 278(50): 50338 - 50345.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
L. Wang, S. H. Lin, W. G. Wu, B. L. Kemp, G. L. Walsh, W. K. Hong, and L. Mao
C-CAM1, a Candidate Tumor Suppressor Gene, Is Abnormally Expressed in Primary Lung Cancers
Clin. Cancer Res., August 1, 2000; 6(8): 2988 - 2993.
[Abstract] [Full Text]


Home page
Cancer Res.Home page
B. B. Singer, I. Scheffrahn, and B. Öbrink
The Tumor Growth-inhibiting Cell Adhesion Molecule CEACAM1 (C-CAM) Is Differently Expressed in Proliferating and Quiescent Epithelial Cells and Regulates Cell Proliferation
Cancer Res., March 1, 2000; 60(5): 1236 - 1244.
[Abstract] [Full Text]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
A. Ohwada, I. Nagaoka, F. Takahashi, S. Tominaga, and Y. Fukuchi
DNA Vaccination against HuD Antigen Elicits Antitumor Activity in a Small-Cell Lung Cancer Murine Model
Am. J. Respir. Cell Mol. Biol., July 1, 1999; 21(1): 37 - 43.
[Abstract] [Full Text]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
M. Muramatsu, M. Oka, Y. Morio, S. Soma, H. Takahashi, and Y. Fukuchi
Chronic hypoxia augments endothelin-B receptor-mediated vasodilation in isolated perfused rat lungs
Am J Physiol Lung Cell Mol Physiol, February 1, 1999; 276(2): L358 - L364.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
I. Nagaoka, Y. Tsutsumi-Ishii, S. Yomogida, and T. Yamashita
Isolation of cDNA Encoding Guinea Pig Neutrophil Cationic Antibacterial Polypeptide of 11 kDa (CAP11) and Evaluation of CAP11 mRNA Expression during Neutrophil Maturation
J. Biol. Chem., September 5, 1997; 272(36): 22742 - 22750.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 1994 American Thoracic Society.
  Red In Translatin