Evidence map›Paper›PMID 31217846›Full record

ArticleAmerican journal of translational research2019

Berberine prevents non-alcoholic steatohepatitis-derived hepatocellular carcinoma by inhibiting inflammation and angiogenesis in mice.

Yan Luo, Guoyan Tian, Zhenjie Zhuang, Jin Chen, Ningning You, Lili Zhuo, Bingtian Liang, Yu Song, Shufei Zang, Juan Liu and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  8. Article
  9. Berberine Induces Combined Cell Death in Gastrointestinal Cell Lines.International journal of molecular sciences · 2023
    Article
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  16. Antiproliferative Effect ofLife (Basel, Switzerland) · 2022
    Article
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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

13 authors at 3 institutions in 1 country.

Yan LuoCollege of Pharmaceutical Science, Zhejiang Chinese Medical University Hangzhou, Zhejiang, China.
Guoyan TianDepartment of Oncology and Hematology, The Affiliated Hospital of Hangzhou Normal University Hangzhou, Zhejiang, China.
Zhenjie ZhuangInstitute of Translational Medicine, The Affiliated Hospital of Hangzhou Normal University Hangzhou, Zhejiang, China.
Jin ChenFourth Clinical Medicine College, Zhejiang Chinese Medical University Hangzhou, Zhejiang, China.
Ningning YouHangzhou Normal University Hangzhou, Zhejiang, China.
Lili ZhuoHangzhou Normal University Hangzhou, Zhejiang, China.
Bingtian LiangFourth Clinical Medicine College, Zhejiang Chinese Medical University Hangzhou, Zhejiang, China.
Yu SongHangzhou Normal University Hangzhou, Zhejiang, China.
Shufei ZangDepartment of Endocrinology, The Affiliated Hospital of Hangzhou Normal University Hangzhou, Zhejiang, China.
Juan LiuDepartment of Pathology, The Affiliated Hospital of Hangzhou Normal University Hangzhou, Zhejiang, China.
Jin YangInstitute of Translational Medicine, The Affiliated Hospital of Hangzhou Normal University Hangzhou, Zhejiang, China.
Weihong GeCollege of Pharmaceutical Science, Zhejiang Chinese Medical University Hangzhou, Zhejiang, China.
Junping ShiInstitute of Translational Medicine, The Affiliated Hospital of Hangzhou Normal University Hangzhou, Zhejiang, China.
Hangzhou Normal University · CNZhejiang Chinese Medical University · CNAffiliated Hospital of Hangzhou Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most malignant and poor prognosis tumors, which was increasingly caused by nonalcoholic fatty liver disease/nonalcoholic steatohepatitis (NAFLD/NASH) in western countries. In this study, we aimed to investigate the mechanism and therapeutic prospect of berberine in the treatment of NASH-HCC mice. Combination of STZ injection and high fat and high-cholesterol diet (HFHC) was used to establish NASH-HCC model. The effect of berberine intervention is studied from histology, biochemistry and molecular level. Our results showed that administration of berberine to NASH-HCC mice reduced the incidence of tumors and mitigated NASH. Berberine significantly reduced the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), glucose (GLU), high-density lipoprotein (HDL), low-density lipoprotein (LDL) and total cholesterol (TC). Transcriptome sequencing and bioinformatics analysis identified numberous genes and various pathways may participate in the favorite effect of berberine. Specifically, berberine suppressed the expressions of genes related to lipogenesis, inflammation, fibrosis and angiogenesis. Moreover, our results showed that berberine suppressed phosphorylation of p38MAPK and ERK as well as COX2 expression significantly. This suggested berberine achieved its biological functions mainly by regulating inflammation and angiogenesis genes involving p38MAPK/ERK-COX2 pathways. This study demonstrated the anti-tumor effects of berberine and its possible mechanism, providing a potential drug for treating NASH-HCC.

Indexed as

angiogenesisBerberineHCCinflammationNASH

Identifiers

PMID31217846
PMCPMC6556646
OpenAlexW2986022110

What OpenQuestion holds

Textmetadata
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.