(N-Stearyl, Norleucine17) VIP hybrid inhibits the growth of pancreatic cancer cell lines

H. Zia, J. Leyton, M. Casibang, V. Hau, D. Brenneman, M. Fridkin, I. Gozes, T. W. Moody

Research output: Contribution to journalArticlepeer-review

Abstract

The effects vasoactive intestinal peptide (VIP) antagonists were investigated on pancreatic cancer cell lines. (N-Stearyl, Norleucine17) VIP hybrid ((SN)VIPhyb) inhibited 125I-VIP binding to human Capan-2 cells with an IC50 value of 0.01 μM whereas VIPhybrid had an IC50 value of 0.2 μM. By RT-PCR and Northern blot, VPAC1 receptor mRNA was detected in CAPAN-2 cells. One μM (SN)VIPhyb and 10 μM VIPhyb inhibited the ability of 30 nM VIP to elevate cyclic AMP and increase c-fos mRNA. (SN)VIPhyb, 1 μM inhibited the clonal growth of CAPAN-2 cells in vitro. In vivo, (SN)VIPhyb (10 μg/day s.c.) inhibited CAPAN-2 xenograft growth in nude mice. These results indicate that (SN)VIPhyb is a pancreatic cancer VPAC receptor antagonist.

Original languageEnglish
Pages (from-to)379-387
Number of pages9
JournalLife Sciences
Volume66
Issue number5
DOIs
StatePublished - 17 Dec 1999

Keywords

  • Pancreatic cancer
  • VIP antagonist
  • c-fos
  • cAMP

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