Effectiveness of p38MAPK activity during drug resistance against HepG2 / 中华肝脏病杂志
Chinese Journal of Hepatology
;
(12): 604-608, 2010.
Article
Dans Chinois
| WPRIM
| ID: wpr-360889
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effectiveness of p38MAPK activity during drug resistance against HepG2.</p><p><b>METHODS</b>HepG2/CDDP kinetic anti-cancer drug resistance model was constructed using anti-cancer drug inducing method and treated with P38MAPK inhibitor SB203580 for 24, 48 and 72 hours respectively. Flow cytometry (FCM) was used to detect the cell cycle distribution. The IC50 of cisplatin was determined by MTT method in vitro. The expressions of P-P38, P-gp, Bcl-2 and Bax were examined by Western blot.</p><p><b>RESULTS</b>The HepG2/CDDP kinetic drug resistance model was successfully established. The expression of P-P38 increased with the increasing drug resistance against HepG2 cells. The models treated with SB203580 could gradually elevate the sensitivity of HepG2/CDDP to cisplatin, block the detention of cell cycle, up-regulate the expression of Bax and down-regulate the expressions of Bcl-2 and P-gp.</p><p><b>CONCLUSION</b>The expression of P-P38 increased with the increasing drug resistance against hepatocellular carcinoma cells. Suppressing the activation of P38 could reverse the drug resistance phenotype against hepatocellular carcinoma cells.</p>
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Phosphorylation
/
Cycle cellulaire
/
Multirésistance aux médicaments
/
Résistance aux médicaments antinéoplasiques
/
P38 Mitogen-Activated Protein Kinases
/
Cellules HepG2
/
Métabolisme
Limites du sujet:
Humains
langue:
Chinois
Texte intégral:
Chinese Journal of Hepatology
Année:
2010
Type:
Article
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