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Resveratrol inhibits the proliferation of A549 cells by inhibiting the expression of COX-2

PURPOSE: The aim was to investigate resveratrol effects on A549 cells proliferation. METHODS: A total of 104 lung adenocarcinoma tissues and nontumor tissues were collected. BEAS-2B cells were cultured in RPMI 1640 medium (group A). A549 cells were treated with RPMI 1640 medium containing different...

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Detalles Bibliográficos
Autores principales: Li, Xia, Li, Fang, Wang, Fangfang, Li, Jinfeng, Lin, Cunzhi, Du, Jianxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973427/
https://www.ncbi.nlm.nih.gov/pubmed/29872310
http://dx.doi.org/10.2147/OTT.S157613
Descripción
Sumario:PURPOSE: The aim was to investigate resveratrol effects on A549 cells proliferation. METHODS: A total of 104 lung adenocarcinoma tissues and nontumor tissues were collected. BEAS-2B cells were cultured in RPMI 1640 medium (group A). A549 cells were treated with RPMI 1640 medium containing different resveratrol concentrations. A549 cells were transfected and grouped as follows: blank group, siRNA-negative control group, siRNA-COX-2 group and resveratrol + siRNA-COX-2 group. qRT-PCR and Western blot were conducted to detect COX-2 expression. MTT assay, soft agar clone assay and flow cytometry were performed to assess proliferation and cell cycle. RESULTS: The relative expression of COX-2 mRNA was significantly increased in lung adenocarcinoma tissues (P<0.01) and it was closely related with clinical stages. Resveratrol at 60 μmol/L significantly inhibited A549 cells proliferation, S phase cells proportion and COX-2 expression (P<0.01). COX-2 expression in siRNA-COX-2 group was significantly lower than that in blank group and siRNA-negative control group (P<0.01). OD(570) values, colony formation rate and S phase cells proportion of resveratrol + siRNA-COX-2 group were much lower than those of other groups (P<0.01). CONCLUSION: Resveratrol inhibits A549 cells proliferation by inhibiting COX-2 expression.