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An adenosine analog (IB-MECA) inhibits anchorage-dependent cell growth of various human breast cancer cell lines.
- Source :
-
The international journal of biochemistry & cell biology [Int J Biochem Cell Biol] 2004 Aug; Vol. 36 (8), pp. 1502-9. - Publication Year :
- 2004
-
Abstract
- A3 adenosine receptor agonists have been reported to influence cell death and survival. Here we report the effects of an A3 adenosine receptor agonist, IB-MECA, on the cell growth of human breast cancer cell lines, MCF-7 (estrogen receptor positive) and MDA-MB468 (estrogen receptor negative). Therefore, this study was aimed to investigate the expression and possible action of A3 receptor in the human breast cancer cell lines. IB-MECA, at 1-100 microM, resulted in a significant cell growth inhibition (P < 0.05) which reached the maximum at 48 h, in the cell lines. In both cell lines, agonist-induced effects were antagonized by pretreatment with a selective A3 adenosine receptor antagonist, MRS1220. Using RT-PCR method, further confirmation was provided by the presence of mRNA of A3 receptor in the cells. In addition, IB-MECA was able to inhibit forskolin-stimulated cAMP levels, which indicate the functional form of A3 receptor on the cell surface of these breast cancer cell lines. These results suggest that the inhibitory effect of IB-MECA on the growth of human breast cancer cell lines is mediated through activation of A3 adenosine receptor.
- Subjects :
- Adenosine A3 Receptor Antagonists
Cell Adhesion
Cell Line, Tumor
Colforsin pharmacology
Cyclic AMP metabolism
Female
Gene Expression Regulation, Neoplastic
Humans
Receptor, Adenosine A3 genetics
Signal Transduction
Adenosine analogs & derivatives
Adenosine pharmacology
Adenosine A3 Receptor Agonists
Breast Neoplasms pathology
Cell Proliferation drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1357-2725
- Volume :
- 36
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- The international journal of biochemistry & cell biology
- Publication Type :
- Academic Journal
- Accession number :
- 15147729
- Full Text :
- https://doi.org/10.1016/j.biocel.2003.12.001