TY - JOUR
T1 - Identification of 1,2,3,4,6-Penta-O-galloyl-β-d-glucopyranoside as a glycine N-methyltransferase enhancer by high-throughput screening of natural products inhibits hepatocellular carcinoma
AU - Kant, Rajni
AU - Yen, Chia Hung
AU - Lu, Chung Kuang
AU - Lin, Ying Chi
AU - Li, Jih Heng
AU - Chen, Yi Ming Arthur
N1 - Funding Information:
This work was supported by the National Research Program for Biopharmaceuticals grant (MOST 104-2325-B-037-002), the Program to Upgrade the R & D Capabilities of Private Universities grant (MOST104-2632-B-037-001) and grant (MOST104-2320-B-037-031-MY3) from the Ministry of Science and Technology, Taiwan. This study was supported partially by the National Health Research Institutes grant (NHRI-104A1-PDCO-0315162), Kaohsiung Medical University “Aim for the Top Universities Grant, Grant Nos. KMU-TP104E11, KMU-TP104E14, KMU-TP104E37, KMU-TP104D07 and KMU-TP104H05”, “Aim for the Top Journals Grant”, Grant No. KMU-DT105004, and Ministry of Health and Welfare grant (MOHW104-TDL-B-212-124-003), Taiwan.
Publisher Copyright:
© 2016 by the authors; licensee MDPI, Basel, Switzerland.
PY - 2016/5/4
Y1 - 2016/5/4
N2 - Glycine N-methyltransferase (GNMT) expression is vastly downregulated in hepatocellular carcinomas (HCC). High rates of GNMT knockout mice developed HCC, while overexpression of GNMT prevented aflatoxin-induced carcinogenicity and inhibited liver cancer cell proliferation. Therefore, in this study, we aimed for the identification of a GNMT inducer for HCC therapy. We established a GNMT promoter-driven luciferase reporter assay as a drug screening platform. Screening of 324 pure compounds and 480 crude extracts from Chinese medicinal herbs resulted in the identification of Paeonia lactiflora Pall (PL) extract and the active component 1,2,3,4,6-penta-O-galloyl- β-D-glucopyranoside (PGG) as a GNMT inducer. Purified PL extract and PGG induced GNMT mRNA and protein expression in Huh7 human hepatoma cells and in xenograft tumors. PGG and PL extract had potent anti-HCC effects both in vitro and in vivo. Furthermore, PGG treatment induced apoptosis in Huh7 cells. Moreover, PGG treatment sensitized Huh7 cells to sorafenib treatment. Therefore, these results indicated that identifying a GNMT enhancer using the GNMT promoter-based assay might be a useful approach to find drugs for HCC. These data also suggested that PGG has therapeutic potential for the treatment of HCC.
AB - Glycine N-methyltransferase (GNMT) expression is vastly downregulated in hepatocellular carcinomas (HCC). High rates of GNMT knockout mice developed HCC, while overexpression of GNMT prevented aflatoxin-induced carcinogenicity and inhibited liver cancer cell proliferation. Therefore, in this study, we aimed for the identification of a GNMT inducer for HCC therapy. We established a GNMT promoter-driven luciferase reporter assay as a drug screening platform. Screening of 324 pure compounds and 480 crude extracts from Chinese medicinal herbs resulted in the identification of Paeonia lactiflora Pall (PL) extract and the active component 1,2,3,4,6-penta-O-galloyl- β-D-glucopyranoside (PGG) as a GNMT inducer. Purified PL extract and PGG induced GNMT mRNA and protein expression in Huh7 human hepatoma cells and in xenograft tumors. PGG and PL extract had potent anti-HCC effects both in vitro and in vivo. Furthermore, PGG treatment induced apoptosis in Huh7 cells. Moreover, PGG treatment sensitized Huh7 cells to sorafenib treatment. Therefore, these results indicated that identifying a GNMT enhancer using the GNMT promoter-based assay might be a useful approach to find drugs for HCC. These data also suggested that PGG has therapeutic potential for the treatment of HCC.
KW - 1,2,3,4,6-penta-O-galloyl-β-d-glucopyranoside (PGG)
KW - Glycine N-methyltransferase (GNMT)
KW - Hepatocellular carcinomas (HCC)
KW - High-throughput screening (HTS)
KW - Sorafenib
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U2 - 10.3390/ijms17050669
DO - 10.3390/ijms17050669
M3 - Article
C2 - 27153064
AN - SCOPUS:84965014175
SN - 1661-6596
VL - 17
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 5
M1 - 669
ER -