Evidence map›Paper›PMID 27153064›Full record

ArticleInternational journal of molecular sciences2016

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.

Rajni Kant, Chia-Hung Yen, Chung-Kuang Lu, Ying-Chi Lin, Jih-Heng Li, Yi-Ming Arthur Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  14. Joint analysis of lncRNA mCancer cell international · 2020
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  20. 1,2,3,4,6-Penta-Frontiers in pharmacology · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Rajni KantInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei 11221, Taiwan. rajnihpmicro@gmail.com.
Chia-Hung YenCenter for Infectious Disease and Cancer Research (CICAR), Kaohsiung Medical University, Kaohsiung 80708, Taiwan. chyen@kmu.edu.tw.
Chung-Kuang LuNational Research Institute of Chinese Medicine, Taipei 11221, Taiwan. cklu@nricm.edu.tw.
Ying-Chi LinSchool of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan. yclin@kmu.edu.tw.
Jih-Heng LiSchool of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan. jhlitox@kmu.edu.tw.
Yi-Ming Arthur ChenCenter for Infectious Disease and Cancer Research (CICAR), Kaohsiung Medical University, Kaohsiung 80708, Taiwan. arthur@kmu.edu.tw.
Kaohsiung Medical University · TWNational Yang Ming Chiao Tung University · TWNational Sun Yat-sen University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinoma, HepatocellularDrug DiscoveryFemaleGlucosidesGlycine N-MethyltransferaseHEK293 CellsHep G2 CellsHigh-Throughput Screening AssaysHumansLiver NeoplasmsMiceMice, Inbred BALB CMice, Nude1,2,3,4,6-penta-O-galloylglucopyranosideAntineoplastic AgentsGlucosidesGlycine N-MethyltransferasePlant Extracts1,2,3,4,6-penta-O-galloyl-β-">d-glucopyranoside (PGG)glycine N-methyltransferase (GNMT)hepatocellular carcinomas (HCC)high-throughput screening (HTS)sorafenib

Identifiers

PMID27153064
PMCPMC4881495
OpenAlexW2345371073

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.