Raf-1 activation suppresses neuroendocrine marker and hormone levels in human gastrointestinal carcinoid cells

被引:76
作者
Sippel, RS
Carpenter, JE
Kunnimalaiyaan, M
Lagerholm, S
Chen, H
机构
[1] Univ Wisconsin, Sch Med, Dept Surg, Clin Sci Ctr H4 750, Madison, WI 53792 USA
[2] Univ Wisconsin, Ctr Comprehens Canc, Madison, WI 53792 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2003年 / 285卷 / 02期
关键词
MAP kinase; signal transduction; neuroendocrine tumors;
D O I
10.1152/ajpgi.00420.2002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Gastrointestinal carcinoid cells secrete multiple neuroendocrine markers and hormones including 5-HT and chromogranin A. The intracellular signaling pathways that regulate production of bioactive molecules are not completely understood. Our aim was to determine whether activation of the raf-1/MEK/MAPK signal transduction pathway in carcinoid cells could modulate production of neuroendocrine markers and hormones. Human pancreatic carcinoid cells (BON) were stably transduced with an estrogen-inducible raf-1 construct creating BON-raf cells. Activation of raf-1 in BON-raf cells led to a marked induction of phosphorylated MEK and ERK1/2 within 48 h. Importantly, raf-1 activation resulted in morphological changes accompanied by a marked decrease in neuroendocrine secretory granules by electronmicroscopy. Moreover, induction of raf-1 in BON-raf cells led to significant reductions in 5-HT, chromogranin A, and synaptophysin levels. Furthermore, treatment of BON-raf cells with MEK inhibitors PD-98059 and U-0126 blocked raf-1-mediated morphological changes and hormone suppression but not ERK1/2 phosphorylation. These results show that raf-1 induction suppresses neuroendocrine marker and hormone production in human gastrointestinal carcinoid cells via a pathway dependent on MEK activation.
引用
收藏
页码:G245 / G254
页数:10
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