GRP-receptor-mediated signal transduction, gene expression and DNA synthesis in the human pancreatic adenocarcinoma cell line HPAF

被引:27
作者
Burghardt, B
Wenger, C
Barabás, K
Rácz, G
Oláh, A
Flautner, L
Coy, DH
Gress, TM
Varga, G
机构
[1] Hungarian Acad Sci, Inst Expt Med, H-1450 Budapest, Hungary
[2] Semmelweis Univ, Dept Surg 1, H-1083 Budapest, Hungary
[3] Semmelweis Univ, Dept Oral Biol, H-1083 Budapest, Hungary
[4] Univ Ulm, Dept Internal Med 1, D-7900 Ulm, Germany
[5] Louisiana State Univ, Med Ctr, Dept Med, New Orleans, LA 70112 USA
关键词
bombesin; antagonist; HPAF; cell line; cell proliferation;
D O I
10.1016/S0196-9781(01)00433-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bombesin-like peptides have been implicated as growth factors in various human cancers. Human adenocarcinoma cell lines (Capan-1, Capan-2, MiaPaCa-2 and HPAF) were tested to determine whether they express the gastrin-releasing peptide-preferring bombesin receptor (GRPR) and neuromedin B-preferring bombesin receptor (NMBR). Using RT-PCR the highest level of GRP receptor mRNA was found in HPAF cells. NMB receptor mRNA expression moderate in all cell lines investigated. We therefore selected the HPAF cell line to investigate whether bombesin treatment affects intracellular Ca2+ ([Ca2+](i)), cAMP level, DNA synthesis as a measure of cell proliferation, and expression of three transcription factors: c-fos, c-myc and high mobility group protein IY (HMG-I(Y)). Bombesin administration led to an immediate increase in free intracellular Ca2+ concentration ([Ca2+](i)) but did not change cAMP levels. The peptide also enhanced [H-3]thymidine incorporation in HPAF cells (but not in the other cell lines), an effect that was concentration dependent, reaching 36 +/- 5% stimulation over control values at 24 h with an EC50, of 2.27 X 10(-12) M. Furthermore, bombesin stimulated c-fos, c-myc and HMG-I(Y) expression in a time-dependent manner: the c-fos mRNA level increased dramatically in the first 30 min of exposure, then returned to basal level within 2 h, while the c-myc and HMG-I(Y) mRNA levels peaked at 2 h and 4h, respectively. All actions of bombesin were blocked by BME (D-Phe(6)-bombesin-(6-13)-methylester), a selective GRP receptor antagonist, but not by the NMB receptor antagonist BIM-23127 (D-Nal-cyclo[Cys-Tyr-D-Trp-Om-Val-Cys]-Nal-NH2). We conclude that HPAF cells express mRNA for GRP receptors and that functional receptors are present in the cell membrane. The occupation of these receptors leads to a sequence of intracellular events involving rapid mobilization of intracellular Ca2+, expression of c-fos, c-myc and HMG-I(Y) mRNA, and stimulation of cell proliferation. Conversely, although NMB receptor mRNA can be detected, its actual translation to functional receptors does not reach a detectable level. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1119 / 1128
页数:10
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