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Molecular Evidence for the Lack of Epidermal Growth Factor Receptor Gene Expression in Small Cell Lung Carcinoma Cells¹

Department of Molecular Biology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, Japan [S. G., J. H., H. H., N. S.]; Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721 [J. H., N. S.]; Division of Pathology, National Cancer Center Research Institute, 5-5-1 Tsukiji, Chuo-ku, Tokyo, Japan [S. H., Y. S.]; and Division of Cancer Biology and Diagnosis, National Cancer Institute, NIH, Bethesda, Maryland 20205 [I. P.]

It has been shown that none of the small cell lung carcinoma (SCLC) cell lines possess epidermal growth factor (EGF) binding activity on their surface. We have examined several SCLC cell lines for the possibility that they may have EGF receptors but that the receptors are masked by an EGF-like protein factor(s), which may be produced by an autocrine mechanism. No evidence, however, was found for the production of such factors. We then used an EGF receptor complementary DNA to determine the state of the EGF receptor gene by Southern blot analysis. The receptor gene appears to be present in these cells in an intact, unrearranged form. These cells, however, were found to lack detectable levels of EGF receptor mRNA, suggesting a possible reason for the absence of EGF receptors on the cell surface. Furthermore, karyotype analysis revealed that SCLC cell lines Lu134 and H69 contained a morphologically normal chromosome 7, which carries the EGF receptor gene. Also, these SCLC cells contained the apparently normal chromosome 3 and exhibited the presence of c-raf-1 gene in an unrearranged form. Thus, the previously noted partial deletion of chromosome 3 is not necessarily common to the SCLC cells. Instead, the lack of EGF receptor is frequently found in SCLC cell lines and is distinct from the other types of lung cancer. We postulate that SCLC cells have some active regulatory mechanism which prevents the expression of EGF receptor gene.

¹ This work was supported in part by a Grant-in Aid from the Ministry of Education, Science and Culture and the Ministry of Health and Welfare, Japan, and a NIH grant.

² To whom requests for reprints should be addressed.

Received 1/21/86. Revised 10/ 7/86. Revised 1/28/87. Accepted 2/16/87.

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