Inhibitory effect of sodium valproate on human lung carcinoma SPC-A1 cell proliferation and the mechanism / 南方医科大学学报
Journal of Southern Medical University
;
(12): 606-609, 2012.
Article
Dans Chinois
| WPRIM
| ID: wpr-267541
ABSTRACT
<p><b>OBJECTIVE</b>To observe the effect of sodium valproate (VPA) on the proliferation and apoptosis of human lung carcinoma SPC-A1 cells and the underlying mechanism.</p><p><b>METHODS</b>The effect of VPA on the proliferation of SPC-A1 cells was evaluated by MTT assay and clone formation assay. Flow cytometry was used to analyze the apoptosis of the cells exposed to VPA. The changes in the expressions of Bcl-xl, Bcl-2, Mcl-1, caspase-9, and caspase-3 in the exposed cells were detected by Western blotting.</p><p><b>RESULTS</b>Incubation with VPA for 48 h resulted in a significant inhibition of SPC-A1 cell proliferation, with a IC(50) of 1.8 mmol/L. VPA treatment also inhibited cell colony formation and induced obvious cell apoptosis. Exposure to 8 mmol/L VPA for 48 h caused a percentage of early apoptotic cells of 60.44%. VPA treatment at different concentrations for 48 h obviously lowered the protein levels of Bcl-xl, Bcl-2, and Mcl-1 and induced caspase-9 and caspase-3 activation in SPC-A1 cells.</p><p><b>CONCLUSION</b>VPA can inhibit the proliferation of SPC-A1 cells by triggering mitochondrion-dependent apoptosis.</p>
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Pharmacologie
/
Acide valproïque
/
Apoptose
/
Protéines proto-oncogènes c-bcl-2
/
Lignée cellulaire tumorale
/
Prolifération cellulaire
/
Protéine bcl-X
/
Caspase-3
/
Caspase-9
/
Protéine Mcl-1
Limites du sujet:
Humains
langue:
Chinois
Texte intégral:
Journal of Southern Medical University
Année:
2012
Type:
Article
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