Activation of the A3 adenosine receptor affects cell cycle progression
and cell growth
R. Brambilla, F. Cattabeni, S. Ceruti, D. Barbieri, C. Franceschi, Y. Kim, K. Jacobson, K. Klotz, M. Lohse, und M. Abbracchio. Naunyn Schmiedebergs Arch Pharmacol, 361 (3):
225-34(März 2000)Brambilla, R Cattabeni, F Ceruti, S Barbieri, D Franceschi, C Kim,
Y C Jacobson, K A Klotz, K N Lohse, M J Abbracchio, M P 01MH30003/MH/NIMH
NIH HHS/United States Research Support, Non-U.S. Gov't Research Support,
U.S. Gov't, P.H.S. Germany Naunyn-Schmiedeberg's archives of pharmacology
Naunyn Schmiedebergs Arch Pharmacol. 2000 Mar;361(3):225-34..
Zusammenfassung
The A3 adenosine receptor has been implicated in modulation of cell
growth. As a first step to the characterization of the underlying
mechanisms, we exposed Chinese hamster ovary (CHO) cells transfected
with the human A3 receptor (A3R-CHO) to selective A3 receptor ligands.
At micromolar concentrations, the A3 agonists N6-(3-iodobenzyl)-adenosine-5'-N-methyluronamide
(IB-MECA) and its 2-chloro derivative Cl-IB-MECA reduced cell number,
with no effects on either parental CHO cells (not expressing any
adenosine receptor), or CHO cells transfected with the human A1 receptor.
Cl-IB-MECA also reduced cell number in the human HEK293 cell line
transfected with the human A3 receptor cDNA as opposed to the respective
untransfected wild-type cells. In A3R-CHO, agonist-induced effects
were antagonized by nanomolar concentrations of A3 antagonists, including
the triazoloquinazoline derivative MRS 1220, the dihydropyridine
derivative MRS 1191, and the triazolonaphthyridine derivative L-249,313.
A3 agonist-induced effects were not due to modulation of cell adhesion,
nor to necrosis or apoptosis. Growth curves revealed highly impeded
growth, and flow-cytometric analysis showed markedly reduced bromodeoxyuridine
incorporation into nuclei. The effect on cell cycle was completely
antagonized by MRS1191. Hence, activation of the human A3 receptor
in A3R-CHO results in markedly impaired cell cycle progression, suggesting
an important role for this adenosine receptor subtype in cell cycle
regulation and cell growth.
Brambilla, R Cattabeni, F Ceruti, S Barbieri, D Franceschi, C Kim,
Y C Jacobson, K A Klotz, K N Lohse, M J Abbracchio, M P 01MH30003/MH/NIMH
NIH HHS/United States Research Support, Non-U.S. Gov't Research Support,
U.S. Gov't, P.H.S. Germany Naunyn-Schmiedeberg's archives of pharmacology
Naunyn Schmiedebergs Arch Pharmacol. 2000 Mar;361(3):225-34.
%0 Journal Article
%1 Brambilla2000
%A Brambilla, R.
%A Cattabeni, F.
%A Ceruti, S.
%A Barbieri, D.
%A Franceschi, C.
%A Kim, Y. C.
%A Jacobson, K. A.
%A Klotz, K. N.
%A Lohse, M. J.
%A Abbracchio, M. P.
%D 2000
%J Naunyn Schmiedebergs Arch Pharmacol
%K & A3 Adenosine Adenosine-5'-(N-ethylcarboxamide)/metabolism Adenosine/*analogs Adenylate Agents/metabolism Analysis Animals Antineoplastic CHO Cell Cells/*drug Cricetinae Cyclase/metabolism Cycle/*drug Cytometry Dihydropyridines/pharmacology Flow Humans Line Membrane/drug P1/antagonists Purinergic Quinazolines/pharmacology Survival/drug Transfection Triazoles/pharmacology Variance derivatives/pharmacology effects effects/enzymology effects/metabolism effects/physiology inhibitors/*drug of Receptor
%N 3
%P 225-34
%T Activation of the A3 adenosine receptor affects cell cycle progression
and cell growth
%U http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10731034
%V 361
%X The A3 adenosine receptor has been implicated in modulation of cell
growth. As a first step to the characterization of the underlying
mechanisms, we exposed Chinese hamster ovary (CHO) cells transfected
with the human A3 receptor (A3R-CHO) to selective A3 receptor ligands.
At micromolar concentrations, the A3 agonists N6-(3-iodobenzyl)-adenosine-5'-N-methyluronamide
(IB-MECA) and its 2-chloro derivative Cl-IB-MECA reduced cell number,
with no effects on either parental CHO cells (not expressing any
adenosine receptor), or CHO cells transfected with the human A1 receptor.
Cl-IB-MECA also reduced cell number in the human HEK293 cell line
transfected with the human A3 receptor cDNA as opposed to the respective
untransfected wild-type cells. In A3R-CHO, agonist-induced effects
were antagonized by nanomolar concentrations of A3 antagonists, including
the triazoloquinazoline derivative MRS 1220, the dihydropyridine
derivative MRS 1191, and the triazolonaphthyridine derivative L-249,313.
A3 agonist-induced effects were not due to modulation of cell adhesion,
nor to necrosis or apoptosis. Growth curves revealed highly impeded
growth, and flow-cytometric analysis showed markedly reduced bromodeoxyuridine
incorporation into nuclei. The effect on cell cycle was completely
antagonized by MRS1191. Hence, activation of the human A3 receptor
in A3R-CHO results in markedly impaired cell cycle progression, suggesting
an important role for this adenosine receptor subtype in cell cycle
regulation and cell growth.
@article{Brambilla2000,
abstract = {The A3 adenosine receptor has been implicated in modulation of cell
growth. As a first step to the characterization of the underlying
mechanisms, we exposed Chinese hamster ovary (CHO) cells transfected
with the human A3 receptor (A3R-CHO) to selective A3 receptor ligands.
At micromolar concentrations, the A3 agonists N6-(3-iodobenzyl)-adenosine-5'-N-methyluronamide
(IB-MECA) and its 2-chloro derivative Cl-IB-MECA reduced cell number,
with no effects on either parental CHO cells (not expressing any
adenosine receptor), or CHO cells transfected with the human A1 receptor.
Cl-IB-MECA also reduced cell number in the human HEK293 cell line
transfected with the human A3 receptor cDNA as opposed to the respective
untransfected wild-type cells. In A3R-CHO, agonist-induced effects
were antagonized by nanomolar concentrations of A3 antagonists, including
the triazoloquinazoline derivative MRS 1220, the dihydropyridine
derivative MRS 1191, and the triazolonaphthyridine derivative L-249,313.
A3 agonist-induced effects were not due to modulation of cell adhesion,
nor to necrosis or apoptosis. Growth curves revealed highly impeded
growth, and flow-cytometric analysis showed markedly reduced bromodeoxyuridine
incorporation into nuclei. The effect on cell cycle was completely
antagonized by MRS1191. Hence, activation of the human A3 receptor
in A3R-CHO results in markedly impaired cell cycle progression, suggesting
an important role for this adenosine receptor subtype in cell cycle
regulation and cell growth.},
added-at = {2010-12-14T18:12:02.000+0100},
author = {Brambilla, R. and Cattabeni, F. and Ceruti, S. and Barbieri, D. and Franceschi, C. and Kim, Y. C. and Jacobson, K. A. and Klotz, K. N. and Lohse, M. J. and Abbracchio, M. P.},
biburl = {https://www.bibsonomy.org/bibtex/2d410a00eaea581a0c63e7f357ab82f06/pharmawuerz},
endnotereftype = {Journal Article},
interhash = {b7e693df94ac4eb1d86d5ca48aa68829},
intrahash = {d410a00eaea581a0c63e7f357ab82f06},
issn = {0028-1298 (Print) 0028-1298 (Linking)},
journal = {Naunyn Schmiedebergs Arch Pharmacol},
keywords = {& A3 Adenosine Adenosine-5'-(N-ethylcarboxamide)/metabolism Adenosine/*analogs Adenylate Agents/metabolism Analysis Animals Antineoplastic CHO Cell Cells/*drug Cricetinae Cyclase/metabolism Cycle/*drug Cytometry Dihydropyridines/pharmacology Flow Humans Line Membrane/drug P1/antagonists Purinergic Quinazolines/pharmacology Survival/drug Transfection Triazoles/pharmacology Variance derivatives/pharmacology effects effects/enzymology effects/metabolism effects/physiology inhibitors/*drug of Receptor},
month = Mar,
note = {Brambilla, R Cattabeni, F Ceruti, S Barbieri, D Franceschi, C Kim,
Y C Jacobson, K A Klotz, K N Lohse, M J Abbracchio, M P 01MH30003/MH/NIMH
NIH HHS/United States Research Support, Non-U.S. Gov't Research Support,
U.S. Gov't, P.H.S. Germany Naunyn-Schmiedeberg's archives of pharmacology
Naunyn Schmiedebergs Arch Pharmacol. 2000 Mar;361(3):225-34.},
number = 3,
pages = {225-34},
shorttitle = {Activation of the A3 adenosine receptor affects cell cycle progression
and cell growth},
timestamp = {2010-12-14T18:20:19.000+0100},
title = {Activation of the A3 adenosine receptor affects cell cycle progression
and cell growth},
url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10731034},
volume = 361,
year = 2000
}