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[Cancer Research 51, 6142-6149, November 15, 1991]
© 1991 American Association for Cancer Research

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Neural Cell Adhesion Molecule Expression and Messenger RNA Splicing Patterns in Lung Cancer Cell Lines Are Correlated with Neuroendocrine Phenotype and Growth Morphology

David P. Carbone1,2, Aurelia M. C. Koros, R. Ilona Linnoila, Philip Jewett and Adi F. Gazdar2

Navy Medical Oncology Branch, National Cancer Institute, Bethesda, Maryland 20889 [D. P. C., I. L., P. J., A. F. G.], and Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania 15261 [A. M. C. K.]

Diverse histological types of lung cancer express neuroendocrine (NE) markers. We studied the expression and alternative splicing forms of the neural cell adhesion molecule (NCAM) NKH-1, a member of the immunoglobulin superfamily, in 56 lung cancer cell lines representing all histological types. We found a strong correlation between expression of NCAM with both NE phenotype and lack of substrate adhesion in culture. Several cell lines expressed high levels of the leukocyte antigen Leu-7 (HNK-1) but were negative for NCAM antigen and mRNA, indicating that the Leu-7 antigen is distinct from NCAM. All of the NCAM-positive cell lines demonstrate a single 6.2-kilobase mRNA, and analysis of the known 3' alternative splices shows predominant expression of only the membrane form with the small intracytoplasmic domain. We conclude that (a) expression of NCAM is associated with NE phenotype regardless of the histological type of lung cancer; (b) these cell lines share a single form of NCAM; (c) with few exceptions, NCAM expression is associated with cell to cell adhesion and lack of substrate adhesion (growing as floating clusters); and (d) Leu-7 antigen is distinct from NCAM. This form of NCAM may play a functional role in NE differentiation or may be a part of the NE program expressed by these cells.

1 To whom requests for reprints should be addressed.

2 Present address: Simmons Cancer Center, University of Texas Southwestern Medical Center, Y9.218, 5323 Harry Hines Boulevard, Dallas, TX 75235-8593.

Received 5/30/91. Accepted 9/11/91.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1991 by the American Association for Cancer Research.