TY - JOUR
T1 - Bombesin stimulates the in vitro growth of a human gastric cancer cell line
AU - Bold, Richard J.
AU - Lowry, Patrick S.
AU - Ishizuka, Jin
AU - Battey, James F.
AU - Townsend, Courtney M.
AU - Thompson, James C.
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1994/12
Y1 - 1994/12
N2 - Bombesin (BBS) and its mammalian equivalent, gastrin‐releasing peptide (GRP) exhibit diverse biological functions, including that of a neurotransmatter, a regulator of gastrointestinal hormone release, and a trophic factor for various normal and neoplastic tissues. Bombesin stimulates the growth of normal cells of the stomach, pancreas, and bronchial epithelium as well as cells in breast cancer, gastrinoma, and small cell lung cancer. The purpose of this study was to determine whether BBS regulates the growth of a human gastric cancer cell line (SIIA) in vitro, and if so, to examine the mechanisms of signal‐transduction that are involved. We found that BBS stimulated the growth of SIIA cells in vitro. The GRP receptor antagonists, BIM 26189 and BIM 26226, had no effect on growth of SIIA cells. Although these antagonists blocked the BBS‐induced increase of [Ca2+]i, they failed to block the growth‐stimulatory effect of BBS. BBS stimulated intracellular tyrosine phosphorylation of multiple proteins, with a predominant protein of apparent molecular weight of 125 kDa. Inhibition of intracellular tyrosine kinases by tyrphostin blocked the growth‐stimulatory effect of BBS on SIIA cells. These results indicate that BBS exerts its trophic effect on SIIA cells through a receptor(s) linked to tyrosine kinase pathway, but not to the phospholipase C (PLC) pathway. © 1994 Wiley‐Liss, Inc.
AB - Bombesin (BBS) and its mammalian equivalent, gastrin‐releasing peptide (GRP) exhibit diverse biological functions, including that of a neurotransmatter, a regulator of gastrointestinal hormone release, and a trophic factor for various normal and neoplastic tissues. Bombesin stimulates the growth of normal cells of the stomach, pancreas, and bronchial epithelium as well as cells in breast cancer, gastrinoma, and small cell lung cancer. The purpose of this study was to determine whether BBS regulates the growth of a human gastric cancer cell line (SIIA) in vitro, and if so, to examine the mechanisms of signal‐transduction that are involved. We found that BBS stimulated the growth of SIIA cells in vitro. The GRP receptor antagonists, BIM 26189 and BIM 26226, had no effect on growth of SIIA cells. Although these antagonists blocked the BBS‐induced increase of [Ca2+]i, they failed to block the growth‐stimulatory effect of BBS. BBS stimulated intracellular tyrosine phosphorylation of multiple proteins, with a predominant protein of apparent molecular weight of 125 kDa. Inhibition of intracellular tyrosine kinases by tyrphostin blocked the growth‐stimulatory effect of BBS on SIIA cells. These results indicate that BBS exerts its trophic effect on SIIA cells through a receptor(s) linked to tyrosine kinase pathway, but not to the phospholipase C (PLC) pathway. © 1994 Wiley‐Liss, Inc.
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U2 - 10.1002/jcp.1041610315
DO - 10.1002/jcp.1041610315
M3 - Article
C2 - 7962132
AN - SCOPUS:0028138316
SN - 0021-9541
VL - 161
SP - 519
EP - 525
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 3
ER -