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[Cancer Research 47, 821-825, February 1, 1987]
© 1987 American Association for Cancer Research

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Selective Stimulation of Small Cell Lung Cancer Clonal Growth by Bombesin and Gastrin-releasing Peptide1

Desmond N. Carney2, Frank Cuttitta, Terry W. Moody and John D. Minna

NCI-Navy Medical Oncology Branch, Division of Cancer Treatment, National Cancer Institute, and Naval Hospital, Bethesda, Maryland 20814-5105 [D. N. C., F. C., J. D. M.]; Department of Biochemistry, George Washington University School of Medicine and Health Science, Washington, DC 20037 [T. W. M.]

Human small cell lung cancers (SCLC) produce and secrete the regulatory peptide bombesin (BN) or its mammalian counterpart gastrinreleasing peptide (GRP). In addition, several SCLC tumor lines have been shown to express high affinity receptors for BN/GRP. On the basis of these findings, we investigated the effect of exogenously added BN and GRP on the soft agarose colony growth of a panel of human cell lines. In serum-free defined medium, colony formation of 9 of 10 SCLC cell lines was stimulated up to 150-fold by BN or GRP, with peak colony stimulation observed at 50 nM BN. In contrast, no stimulatory effect of BN was observed on nine non-SCLC cell lines. Although no stimulation of colony growth by BN was seen in serum-supplemented medium, addition of BN to the serum-free medium increased cloning efficiency to that achieved by serum in most of the SCLC cell lines. GRP 1–27, the active mammalian analogue of Bn, stimulated colony growth of SCLC cells similar to the manner of BN, while the physiologically inactive BN analogue, des-Leu (13)-Met (14)-BN, had no effect on colony growth. No correlation was observed in SCLC cell lines between the response of these cells to exogenous BN and the amount of cellular BN/GRP produced or the presence of BN receptors. These data suggest that BN/GRP may in some instances function as an autocrine growth factor for SCLC and indicate new ways for modulating SCLC growth in patients with this tumor.

1 The opinions or assertions herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Department of the Navy or the Department of Defense.

2 To whom requests for reprints should be addressed, at Mater Hospital, Dublin 7, Ireland.

Received 5/ 5/86. Revised 10/ 3/86. Accepted 10/14/86.




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Copyright © 1987 by the American Association for Cancer Research.