Tumor types expressing a neuroendocrine phenotype secrete neuropeptides wit
h paracrine or autocrine growth factor activity. The efficacy of these para
crine or autocrine loops depends on the expression of specific receptors on
tumor cells. Once specific receptors are identified, specific neuropeptide
antagonists disrupting paracrine and autocrine loops could be potential tr
eatments in neuropeptide-secreting tumors. In the present study, 11 human t
umor cell lines representing astrocytoma, lymphoma, and pancreatic, prostat
e, lung and colon carcinomas were examined for expression of five different
neuropeptide receptors (cholecystokinin, neurotensin, vasopressin, tachyki
nine substance P and cannabinoid) using RT-PCR and radioligand binding. The
presence of various neuropeptide receptors in different human cancer cell
lines supports development of new antitumor treatments based on disruption
of neuropeptide autocrine growth pathways. [(C) 2001 Lippincott Williams &
Wilkins.].