Effect of Recombinant Monokines, Lymphokines, and Other Agents on Clonal Proliferation of Human Lung Cancer Cell Lines1

The modulation of donai growth of cells of 15 human lung cancer lines was examined by coculture with different recombinant lymphokines, monokines, and several agents which induce differentiation in other malignant cell systems. Recombinant human tumor necrosis factor a (TNF) was inhibitory to all non-small cell lung cancer cell lines with a 50% effective dose of donai inhibition (EDM) in the range of 30-2000 units/ml. Two representative squamous lines (SK-MES and P.,) had 150 to 250 high affinity (A"d~ p.\i) cell surface TNF receptors. In contrast, clonal growth of small cell lung cancer lines was not inhibited by TNF, and two representative lines (H69c and R592) expressed negligible cell surface TNF receptors. Recombinant a, ß, and y interferons (4000 units/ ml) each inhibited >30% clonal growth of more than 50% of the nonsmall cell lung cancer lines. TNF (100-1000 units/ml) in combination with •y-interferon was synergistic in the inhibition of clonal growth of these cells. Further studies showed that synergism of clonal inhibition occurred even when the cells were initially exposed to Y-interferon, washed, and plated in soft agar with TNF. All-fra/u-retinoic acid (EDjo, 5 x Ifl-'-lO-6 M), dimethyl sulfoxide (ED», 1.2-1.6%), and 12-0tetradecanoylphorbol-13-acetate (ED», 5 x lO-'-lO'10 M) inhibited clonal proliferation of 7 of 9, 7 of 9, and 8 of 9 non-small cell lung cancer lines, respectively. In contrast, clonal proliferation of cells of small cell lung cancer lines was decreased only slightly at almost all concentrations of each of the agents. Interleukin-1 and -2 and granulocyte-monocyte colony-stimulating factor had no effect on the clonal growth of any of the lung cancer lines. Our results suggest that TNF in combination with 7interferon may be therapeutical!}' active for some patients with non-small cell lung cancer, but small cell lung cancer probably will be unresponsive to all the agents that we examined.