2023
DOI: 10.29219/fnr.v67.9244
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In vitro anti-hepatocellular carcinogenesis of 1,2,3,4,6-Penta-O-galloyl-β-D-glucose

Abstract: Background: 1,2,3,4,6-Penta-O-galloyl-β-D-glucose (β-PGG) is a polyphenol ellagic compound with a variety of pharmacological effects and has an inhibitory effect on lots of cancers. Objective: To explore the antitumor effects and mechanism of 1,2,3,4,6-Penta-O-galloyl-β-D-glucose on human hepatocellular carcinoma HepG2 cells. Design: A network pharmacology method was first used to predict the possible inhibition of hepatocellular carcinoma growth by 1,2,3,4,6-Penta-O-galloyl-β-D-glucose (β-PGG) thr… Show more

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Cited by 3 publications
(2 citation statements)
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References 38 publications
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“…Peaks 8 and 2 could not be identified because of experimental limitations, which also was the shortcoming of this experiment, and subsequent studies will be combined with mass spectrometry to help identify more compounds in HG and BG. PGG has shown strong biological and pharmacological activities in antiviral, anticancer, anti-inflammatory, antimicrobial, and antidiabetic [ 27 ]. There are diverse scientific reports on the biological and pharmacological activities of GA, focused on antioxidant, antimicrobial, anti-inflammatory, anticancer, cardioprotective, gastroprotective, and neuroprotective effects [ 28 ].…”
Section: Resultsmentioning
confidence: 99%
“…Peaks 8 and 2 could not be identified because of experimental limitations, which also was the shortcoming of this experiment, and subsequent studies will be combined with mass spectrometry to help identify more compounds in HG and BG. PGG has shown strong biological and pharmacological activities in antiviral, anticancer, anti-inflammatory, antimicrobial, and antidiabetic [ 27 ]. There are diverse scientific reports on the biological and pharmacological activities of GA, focused on antioxidant, antimicrobial, anti-inflammatory, anticancer, cardioprotective, gastroprotective, and neuroprotective effects [ 28 ].…”
Section: Resultsmentioning
confidence: 99%
“…A duration of 24 h after transfection, the supernatant and washing liquid of each group of cells were collected, the cells were digested with 0.25% trypsin (without EDTA), centrifuged together with the above supernatant and culture medium, and were washed twice with PBS. Preprepared 1× Annexin V Binding solution was used to prepare a cell suspension with a final concentration of 1 × 106 cells/mL [46,47]. The apoptosis rate was measured by flow cytometry (FACSVerse, Becton, Dickinson and Company, Franklin Lakes, NJ, USA).…”
Section: Flow Cytometrymentioning
confidence: 99%