Influence of all-trans retinoic acid in proliferation, migration and invasion of human hepatocellular carcinoma SMMC-7721 cells and its molecular mechanism
Fengxia Huang
Abstract
Fengxia Huang
Abstract
Objective To investigate the influence of all-trans retinoic acid(ATRA) in proliferation,migration and invasion of human hepatocellular carcinoma SMMC-7721 cells and to clarity its molecular mechanism.Methods The SMMC-7721 cells in logarithmic phase were divided into blank control group and 10,20,and 40 μmol·L-1 ATRA groups.The proliferation ability of SMMC-7721 cells was examined by MTS/PMS assay,and the migration and invasion abilities of SMMC-7721 cells were detected by Wound Healing assay and Transwell assay,and the expressions of MMP-9 mRNA and protein in SMMC-7721 cells were determined by Real-time PCR and Western blotting methods.Results Compared with blank control group,the proliferation rates in 20 and 40 μmol·L-1 ATRA groups were decreased significantly(P0.01).Wound Healing assay discovered that the scuffing distance of SMMC-7721 cells exposed to 20 and 40 μmol·L-1 ATRA for 24 h was significantly increased compared with blank control group(P0.05).Transwell assay showed that the numbers of SMMC-7721 cells migrated through the matrigel in 10,20,and 40 μmol·L-1 ATRA groups 24 h after treatment were obviously decreased compared with blank control group(P0.05).The Real-time PCR and Western blotting results showed that the expressions of MMP-9 mRNA and protein in SMMC-7721 cells in 20 and 40 μmol·L-1 ATRA groups 24 h after treatment were significantly decreased compared with blank control group(P0.01).Conclusion ATRA may inhibit the proliferation,migration and invasion of human hepatocellular carcinoma SMMC-7721 cells,which may be related to the down-regulation of MMP-9.
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Objective To investigate the influence of all-trans retinoic acid(ATRA) in proliferation,migration and invasion of human hepatocellular carcinoma SMMC-7721 cells and to clarity its molecular mechanism.Methods The SMMC-7721 cells in logarithmic phase were divided into blank control group and 10,20,and 40 μmol·L-1 ATRA groups.The proliferation ability of SMMC-7721 cells was examined by MTS/PMS assay,and the migration and invasion abilities of SMMC-7721 cells were detected by Wound Healing assay and Transwell assay,and the expressions of MMP-9 mRNA and protein in SMMC-7721 cells were determined by Real-time PCR and Western blotting methods.Results Compared with blank control group,the proliferation rates in 20 and 40 μmol·L-1 ATRA groups were decreased significantly(P0.01).Wound Healing assay discovered that the scuffing distance of SMMC-7721 cells exposed to 20 and 40 μmol·L-1 ATRA for 24 h was significantly increased compared with blank control group(P0.05).Transwell assay showed that the numbers of SMMC-7721 cells migrated through the matrigel in 10,20,and 40 μmol·L-1 ATRA groups 24 h after treatment were obviously decreased compared with blank control group(P0.05).The Real-time PCR and Western blotting results showed that the expressions of MMP-9 mRNA and protein in SMMC-7721 cells in 20 and 40 μmol·L-1 ATRA groups 24 h after treatment were significantly decreased compared with blank control group(P0.01).Conclusion ATRA may inhibit the proliferation,migration and invasion of human hepatocellular carcinoma SMMC-7721 cells,which may be related to the down-regulation of MMP-9.
Key concepts: Retinoic acid, Blot, Matrigel, Hepatocellular carcinoma, Molecular biology, Wound healing, Gentamicin protection assay, Chemistry