Abstract | OBJECTIVE: To determine the effect of nylestriol and levonorgestrel on mRNA expression of OPG/OPGL in MG-63 cell lines, and to explore whether the paracrine effect is involved in the regulation course. Methods Semi-quantitive RT-PCR was conducted to analyze mRNA expression of OPG/OPGL in MG-63 cell lines treated with nylestriol and levonorgestrel. Results Both medicines could stimulate MG-63 cell lines to express OPG, and the best action levels of the two medicines were 10(-6) mol/L. Both medicines could decrease mRNA expression levels of OPGL dramatically. In NYL 10(-10) mol/L treatment group, medium renewal has negative effect on mRNA expression of OPG. Conclusion Both the two medicines can promote mRNA expression of OPG in MG-63 cell lines, while decrease mRNA expression of OPGL. The paracrine effect of MG-63 cell lines may be involved in the regulation of mRNA expression of OPG by NYL.
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Authors | Kai-chu Yang, Er-yuan Liao, Hou-de Zhou, Xin-hua Xiao |
Journal | Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
(Zhong Nan Da Xue Xue Bao Yi Xue Ban)
Vol. 29
Issue 6
Pg. 667-70
(Dec 2004)
ISSN: 1672-7347 [Print] China |
PMID | 16114553
(Publication Type: Journal Article)
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Chemical References |
- Carrier Proteins
- Glycoproteins
- Membrane Glycoproteins
- Osteoprotegerin
- RANK Ligand
- RNA, Messenger
- Receptor Activator of Nuclear Factor-kappa B
- Receptors, Cytoplasmic and Nuclear
- Receptors, Tumor Necrosis Factor
- TNFRSF11A protein, human
- TNFRSF11B protein, human
- TNFSF11 protein, human
- Levonorgestrel
- nylestriol
- Quinestrol
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Topics |
- Carrier Proteins
(biosynthesis, genetics)
- Female
- Glycoproteins
(biosynthesis, genetics)
- Humans
- Levonorgestrel
(pharmacology)
- Membrane Glycoproteins
(biosynthesis, genetics)
- Osteoprotegerin
- Osteosarcoma
(pathology)
- Quinestrol
(analogs & derivatives, pharmacology)
- RANK Ligand
- RNA, Messenger
(biosynthesis, genetics)
- Receptor Activator of Nuclear Factor-kappa B
- Receptors, Cytoplasmic and Nuclear
(biosynthesis, genetics)
- Receptors, Tumor Necrosis Factor
(biosynthesis, genetics)
- Tumor Cells, Cultured
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