Abstract
Functional VIP/PACAP receptors were identified in the human glioblastoma cell line T98G, based on the relative potency of VIP, PACAP and PACAP-38 to stimulate adenylate cyclase activity. Analysis of the T98G cells mRNA by reverse transcription followed by a polymerase chain reaction (RT-PCR) demonstrated the expression of the mRNA coding for the VIP2 receptor subclass only. VIP, PACAP-27 and PACAP-38 were potent and efficIent inhibitors of cell proliferation, assessed by the colorimetric MTT assay. VIP, PACAP-27 and PACAP-38 also reduced the incorporation of 3H-thymidine in T98G cells, but did not significantly alter the percentage of cells present at each stage of the cell cycle. Thus, VIP and PACAP, probably acting through a VIP2 receptor subtype, decreased cell proliferation.
Publication types
-
Comparative Study
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adenylyl Cyclases / metabolism*
-
Brain Neoplasms / pathology*
-
Cell Cycle / drug effects
-
Cell Division / drug effects
-
DNA Replication / drug effects
-
DNA, Neoplasm / biosynthesis
-
Enzyme Activation / drug effects
-
Glioblastoma / pathology*
-
Growth Inhibitors / pharmacology*
-
Humans
-
Neoplasm Proteins / drug effects*
-
Neoplasm Proteins / physiology
-
Neuropeptides / pharmacology*
-
Pituitary Adenylate Cyclase-Activating Polypeptide
-
Polymerase Chain Reaction
-
RNA, Messenger / biosynthesis
-
Receptors, Vasoactive Intestinal Peptide / drug effects*
-
Receptors, Vasoactive Intestinal Peptide / physiology
-
Receptors, Vasoactive Intestinal Peptide, Type II
-
Tumor Cells, Cultured / drug effects
-
Vasoactive Intestinal Peptide / pharmacology*
Substances
-
ADCYAP1 protein, human
-
DNA, Neoplasm
-
Growth Inhibitors
-
Neoplasm Proteins
-
Neuropeptides
-
Pituitary Adenylate Cyclase-Activating Polypeptide
-
RNA, Messenger
-
Receptors, Vasoactive Intestinal Peptide
-
Receptors, Vasoactive Intestinal Peptide, Type II
-
Vasoactive Intestinal Peptide
-
Adenylyl Cyclases