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Immunocytochemical Detection of Human Lung Cancer Heterogeneity Using Antibodies to Epithelial, Neuronal, and Neuroendocrine Antigens¹

Department of Pathology, University of Nijmegen, Geert Grooteplein Zuid 24, 6525 GA Nijmegen [J. L. V. B., M. K. R., T. O., A. H., A. J. M. W-v. T., G. P. V., F. C. S. R.], and Department of Pathology, St. Antonius Hospital, Nieuwegein [S. S. W.], The Netherlands

Lung cancers were investigated for their heterogeneity as expressed by their immunoreactivity for cytokeratins and neurofilament proteins, as well as for the neuroendocrine differentiation antigen MOC-1. Using broadly cross-reacting antibodies, cytokeratins were detected in nearly all cases of lung carcinomas. Keratinization could be detected only in cases of moderately to well-differentiated squamous cell carcinoma (SQC) using a monoclonal antibody to cytokeratin 10, while a monoclonal antibody reactive with cytokeratin 18, and specific for glandular epithelia, reacted with adenocarcinomas, small cell lung carcinomas (SCLC), and lung carcinoids. In SQC this antibody could detect non-squamous cell differentiation, showing increasing numbers of positive cells with decrease of histologically detectable SQC differentiation. Cells positive for neurofilaments were demonstrated in some of the poorly differentiated SQCs and in some of the cases of SCLC, possibly representing the variant type of SCLC. Also in some of the lung carcinoids neurofilament proteins were present, colocalizing with cytokeratins. MOC-1 was present in all SCLC and lung carcinoids. This antibody could also detect neuroendocrine differentiation in all combined small cell carcinomas, in one poorly differentiated adenocarcinoma, and in about 30% of the poorly differentiated SQCs. Therefore, lung cancer heterogeneity can be detected using a panel of well-defined antibodies to intermediate filaments in combination with the MOC-1 antibody. The use of these antibodies in diagnosis can have prognostic significance and can lead to a more selective therapeutic approach.

¹ This study was supported by Netherlands Cancer Foundation Grant NUKC 1984-13.

² To whom requests for reprints should be addressed.

Received 7/14/86. Revised 11/14/86. Revised 3/ 4/87. Accepted 3/10/87.

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