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Resveratrol Inhibits Hepatocellular Carcinoma Progression through Regulating Exosome Secretion
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Background and Objectives:
Resveratrol is a promising drug for tumor therapy,
but its anti-tumor mechanism remains unclarified. The present study aimed to explore
the effect of resveratrol on the secretion of exosomes and the role of resveratrol-induced
exosomes in the progression of hepatocellular carcinoma.
Methods:
The number and contents of exosomes induced by resveratrol were determined
by nanoparticle tracking analysis and high-throughput sequencing in Huh7 cells, respectively.
Expression of Rab27a was assessed by Western blotting and immunofluorescence.
Cell proliferation, migration and epithelial-mesenchymal transition were examined with
the stimuli of resveratrol and exosomes, the activity of autophagy and wnt/β-catenin signaling
induced by resveratrol-induced exosomes and knockdown of lncRNA SNHG29
were monitored by Western blotting and immunofluorescence.
Results:
It was found that resveratrol might inhibit the exosome secretion by down-regulating
the expression of Rab27a, thereby suppressing the proliferation, migration and
epithelial-mesenchymal transition of Huh7 cells. Moreover, resveratrol-induced exosomes
could also inhibit the malignant phenotype of Huh7 cells via inhibiting the nuclear
translocation of β-catenin and the activation of autophagy, which lncRNA SNHG29
might mediate.
Conclusion:
Resveratrol inhibits hepatocellular carcinoma progression by regulating exosome
secretion and contents.
Bentham Science Publishers Ltd.
Title: Resveratrol Inhibits Hepatocellular Carcinoma Progression through
Regulating Exosome Secretion
Description:
Background and Objectives:
Resveratrol is a promising drug for tumor therapy,
but its anti-tumor mechanism remains unclarified.
The present study aimed to explore
the effect of resveratrol on the secretion of exosomes and the role of resveratrol-induced
exosomes in the progression of hepatocellular carcinoma.
Methods:
The number and contents of exosomes induced by resveratrol were determined
by nanoparticle tracking analysis and high-throughput sequencing in Huh7 cells, respectively.
Expression of Rab27a was assessed by Western blotting and immunofluorescence.
Cell proliferation, migration and epithelial-mesenchymal transition were examined with
the stimuli of resveratrol and exosomes, the activity of autophagy and wnt/β-catenin signaling
induced by resveratrol-induced exosomes and knockdown of lncRNA SNHG29
were monitored by Western blotting and immunofluorescence.
Results:
It was found that resveratrol might inhibit the exosome secretion by down-regulating
the expression of Rab27a, thereby suppressing the proliferation, migration and
epithelial-mesenchymal transition of Huh7 cells.
Moreover, resveratrol-induced exosomes
could also inhibit the malignant phenotype of Huh7 cells via inhibiting the nuclear
translocation of β-catenin and the activation of autophagy, which lncRNA SNHG29
might mediate.
Conclusion:
Resveratrol inhibits hepatocellular carcinoma progression by regulating exosome
secretion and contents.
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