Abstract

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.

Highlights

  • Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies and deadliest cancers [1,2]

  • Basal luciferase activity measured in Huh7 GNMT promoter-luciferase (H7GPL) cells confirmed the presence of the reporter fragment (Figure 1a)

  • We further evaluated the qualification of H7GPL cells as a drug screening platform with Suberoylanilide hydroxamic acid (SAHA)

Read more

Summary

Introduction

Hepatocellular carcinoma (HCC) is one of the most prevalent malignancies and deadliest cancers [1,2]. Only sorafenib has been approved for the treatment of HCC [3,4] It has side effects, and patients quickly develop resistance to it [5,6]. GNMT has protective effects against exposure to various carcinogens, including aflatoxins and polyaromatic hydrocarbons [10,11]. It is downregulated in the tumorous tissues of >80% HCC patients, as well as in the livers of cirrhotic patients who were at risk of developing HCC [12,13]. Transgenic mice with human GNMT overexpression in their livers resisted aflatoxin B1-induced liver tumorigenesis [10]. We further characterized the inhibitory function of PGG on HCC both in vitro and in vivo

Results
Cell Culture and Reagents
Plasmids and Transfections
Development of GNMT Expression-Oriented Drug Screening Platform
Immunoblotting
Cell Viability and Colony Formation Assay
Flow Cytometry
In Vivo Tumor Models
4.10. Statistical Analysis
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.