HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

M2 muscarinic receptors inhibit cell proliferation in human glioblastoma cell lines.

AbstractAIMS:
In the present work we investigated the expression of M2 muscarinic receptor subtype in two glioblastoma cell lines and its role in the control of cell proliferation.
MAIN METHODS:
The M2 receptor transcript and protein expression was studied using RT-PCR and western blot analysis. (3)[H]-thymidine incorporation was used to evaluate cell proliferation in the presence or in the absence of M(2) agonist arecaidine.
KEY FINDINGS:
We demonstrated that M(2) receptor is expressed in both cell lines, although U251 cells show a higher expression level, compared to U87 cells. The activation of M(2) receptors by the agonist arecaidine decreases cell growth in a dose and time dependent manner. The anti-proliferative effect of arecaidine is also confirmed by the significant decrease of (3)[H]-thymidine incorporation in both cell lines. Moreover the M2 antagonist gallamine counteracts the arecaidine effects confirming M2 receptor involvement in glioma cell growth inhibition.
SIGNIFICANCE:
These data suggest a role for M2 receptors in the inhibition of glioma cell proliferation and the possibility of exploiting these receptors as new promising tools for glioblastoma therapy.
AuthorsM Ferretti, C Fabbiano, M Di Bari, D Ponti, A Calogero, A M Tata
JournalLife sciences (Life Sci) Vol. 91 Issue 21-22 Pg. 1134-7 (Nov 27 2012) ISSN: 1879-0631 [Electronic] Netherlands
PMID22575825 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • Receptor, Muscarinic M2
  • arecaidine
  • Arecoline
Topics
  • Arecoline (analogs & derivatives, pharmacology)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Gene Expression Regulation, Neoplastic
  • Glioblastoma (drug therapy, genetics, metabolism, pathology)
  • Humans
  • Receptor, Muscarinic M2 (agonists, antagonists & inhibitors, genetics, metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: