PubMed · 1992 · 83 citations · 15 references
MedicineOncologyPharmacologyCancer PharmacologyCell SignalingSignal TransductionCancer Cell SignalingOncology PharmacologyAnticancer ActivityAnticancer ChemotherapyAutocrine LoopsCancer Cell Proliferation InhibitionNeuropeptide AntagonistsSmall Cell Lung Cancer TherapySmall Cell Lung Cancer Treatment
The proliferation of small cell lung cancer (SCLC) cells appears sustained by multiple autocrine and paracrine circuits involving Ca2+ mobilizing neuropeptides. Consequently, broad spectrum neuropeptide antagonists which inhibit SCLC growth in vitro have been suggested as potential anticancer agents. Here we evaluated this hypothesis using xenografts of WX322 cells, a SCLC cell line that responds to multiple Ca2+ mobilizing neuropeptides. The broad spectrum neuropeptide antagonists [Arg6,D-Trp7,9,MePhe8]substance P(6-11) and [D-Arg1,D-Phe5,Trp7,9Leu11[substance P were shown to inhibit the growth of WX322 xenografts in nude mice. Similar results were obtained with xenografts of the SCLC cell line H69. The results indicate that broad spectrum neuropeptide antagonists can inhibit the growth of SCLC in vivo and suggest that these antagonists could be useful in the treatment of SCLC.
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Bombesin-like peptides can function as autocrine growth factors in human small-cell lung cancer
Frank Cuttitta, Desmond N. Carney, James L. Mulshine et al. · Nature · 1985 · 1.4K citations
Medicine, Cancer Biology, Oncology +11
Hormone production by cultures of small-cell carcinoma of the lung
George D. Sorenson, Olive S. Pettengill, Truls Brinck‐Johnsen et al. · Cancer · 1981 · 201 citations · Full text
Penella J. Woll, Enrique Rozengurt · Proceedings of the National Academy of Sciences · 1988 · 173 citations · Full text
Medicine, Oncology, Pharmacology +13