Evidence map›Paper›PMID 34040893›Full record

ArticlePeerJ2021

DZNep, an inhibitor of the histone methyltransferase EZH2, suppresses hepatic fibrosis through regulating miR-199a-5p/SOCS7 pathway.

Rongrong Ding, Jianming Zheng, Ning Li, Qi Cheng, Mengqi Zhu, Yanbing Wang, Xinlan Zhou, Zhanqing Zhang, Guangfeng Shi

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  9. Novel Therapeutic Targets in Liver Fibrosis.Frontiers in molecular biosciences · 2021
    Review
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

9 authors at 3 institutions in 1 country.

Rongrong DingInfectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Jianming ZhengInfectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Ning LiInfectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Qi ChengInfectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Mengqi ZhuInfectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Yanbing WangHepatobiliary Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Xinlan ZhouHepatobiliary Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Zhanqing ZhangHepatobiliary Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Guangfeng ShiInfectious Diseases, Huashan Hospital, Fudan University, Shanghai, China.
Fudan University · CNShanghai Public Health Clinical Center · CNHuashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatic fibrosis is a common response to chronic liver injury. Recently, the role of DZNep (a histone methyltransferase EZH2 inhibitor) in repressing pulmonary and renal fibrosis was verified. However, the potential effect of DZNep on hepatic fibrosis has not been elucidated.

methodsThe hepatic fibrosis model was established in rats treated with CCl4 and in hepatic stellate cells (HSCs) treated with TGF-

resultsThe EZH2 level was increased in CCl4-treated rats and in TGF-

conclusionsDZNep suppresses hepatic fibrosis through regulating miR-199a-5p/SOCS7 axis, suggesting that DZNep may represent a novel treatment for fibrosis.

Indexed as

DZNepEZH2Hepatic fibrosismiR-199a-5pSOCS7TGF-β1

Identifiers

PMID34040893
PMCPMC8127960
OpenAlexW3161240057

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.