The proliferative response of HT-29 human colon adenocarcinoma cells to bombesin-like peptides

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• 作者：Cassano ; Giuseppe ; Resta ; Nicoletta ; Gasparre ; Giuseppe ; Lippe ; Claudio ; Guanti ; Ginevra
• 关键词：Colorectal-cancer ; Bombesin ; Gastrin-releasing-peptide ; Neuromedin-B ; Neuromedin-C ; Reverse-transcription-polymerase-chain-reaction
• 刊名：Cancer Letters
• 出版年：2001
• 出版时间：October 30, 2001
• 年：2001
• 卷：172
• 期：2
• 页码：151-157
• 全文大小：1.44 M

文摘

Bombesin-like peptides (BLP) and their receptors are widely distributed throughout the intestine and are potential mitogens for gastrointestinal cancers. In this study we characterized the proliferation induced by BLP in the human adenocarcinoma cell line HT-29. The number of HT-29 cells, partially serum deprived (1 % fetal bovine serum) for 48 h, was increased after 24 h of stimulation with bombesin, GRP, neuromedin B (NMB) and neuromedin C (NMC) ranging from 0.1 nM up to 1 μM. Reverse transcription polymerase chain reaction studies, revealed the presence of mRNA for NMB and for the GRP preferring receptor (GRP-R). mRNA for GRP, NMB preferring receptor (NMB-R) and bombesin receptor subtype 3 (BRS-3) were not detected. [d-Phe⁶]bombesin-(6-13)methyl ester (A1) and BIM-23127 (A2), are considered as inhibitors of binding to GRP-R and NMB-R, respectively. Surprisingly, A1 and A2 stimulated the proliferation of HT-29 cells. Moreover, in the simultaneous presence of 1 μM A1 and 0.1 μM GRP or 0.1 nM or 0.1 μM bombesin, inhibition of the proliferation was observed. Our data demonstrate that the proliferation induced by BLP in HT-29 cells is due to interaction with the GRP-R.