The helix-loop-helix protein Id2 is overexpressed in human pancreatic cancer

被引:0
作者
Kleeff, J
Ishiwata, T
Friess, H
Büchler, MW
Israel, MA
Korc, M
机构
[1] Univ Calif Irvine, Div Endocrinol Diabet & Metab, Dept Med, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92697 USA
[4] Univ Bern, Dept Visceral & Transplantat Surg, CH-3010 Bern, Switzerland
[5] Univ Calif San Francisco, Dept Neurol Surg, Preuss Lab, San Francisco, CA 94143 USA
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Id2 belongs to the Id family of helix-loop-helix (HLH) proteins, which upon heterodimerization with basic HLH proteins prevent basic HLH proteins from DNA binding. Proteins of the Id family act as negative regulatory transcriptional factors, and their expression correlates with cell proliferation and arrested differentiation in many cell lineages. In this study, we characterized the expression of Id2 in normal and cancerous pancreatic tissues. Pancreatic cancers markedly overexpressed Id2 mRNA in comparison to the normal pancreas. Furthermore, there was abundant Id2 immunoreactivity in the cancer cells within the pancreatic tumor mass. In PANC-1 human pancreatic cancer cells, steady-state Id2 mRNA levels increased upon serum addition and decreased after induction of differentiation with either sodium butyrate or 12-O-tetradecanoylphorbol-13-acetate. Inhibition of Id2 expression with Id2 antisense oligonucleotides inhibited the growth of these cells, whereas random and sense oligonucleotides were without effect. These findings suggest that Id2 may have a role in human pancreatic cancer.
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页码:3769 / 3772
页数:4
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