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Journal of Southern Medical University ; (12): 1624-1627, 2015.
Article Dans Chinois | WPRIM | ID: wpr-232558

Résumé

<p><b>OBJECTIVE</b>To investigate the expression of microRNA-100(miR-100) and the relationship with cisplatin resistance in human ovarian epithelial cancer SKOV3/DDP cells.</p><p><b>METHODS</b>The SKOV3/DDP cells were transfected with the mimics or inhibitor of miR-100 or negative control RNA (NC) or inhibitor negative control RNA (inhibitor NC) by lipofectamine 2000. The experiment was divided into six groups: SKOV3 group, SKOV3/DDP group, miR-100 mimices group, NC group, miR-100 inhibitor group and inhibitor NC group. The expression of miR-100 and the cisplatin IC50 were measured by real-time PCR and CCK8 assay respectively.</p><p><b>RESULTS</b>(1)The cisplatin resistance index of SKOV3/DDP was 2.23; (2)The express level of miR-100 in SKOV3/DDP cells was significantly lower than that in SKOV3 cells (P<0.001); (3)After transfected with miR-100 mimics, SKOV3/DDP cells showed that the level of miR-100 was 38.29 times higher than that in the NC group(P<0.01). The cisplatin IC50 of miR-100 mimices group was significantly lower than that in the NC group (P<0.001); (4) After transfected with miR-100 inhibitor, the level of miR-100 0f SKOV3/DDP was decreased by 97.7%. The cisplatin IC50 of miR-100 inhibitor group was significantly increased as compared with that in the inhibitor NC group (P<0.001).</p><p><b>CONCLUSION</b>The expression of miR-100 is downregulated in SKOV3/DDP cells. Overexpressing miR-100 may effectively increase the sensitivity to cisplatin of human ovarian epithelial cancer SKOV3/DDP cells and may reverse cisplatin-resistance of EOC (epithelial ovarian cancer).</p>


Sujets)
Femelle , Humains , Antinéoplasiques , Lignée cellulaire tumorale , Cisplatine , Pharmacologie , Régulation négative , Résistance aux médicaments antinéoplasiques , microARN , Métabolisme , Tumeurs épithéliales épidermoïdes et glandulaires , Métabolisme , Anatomopathologie , Tumeurs de l'ovaire , Métabolisme , Anatomopathologie , Réaction de polymérisation en chaine en temps réel , Transfection
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