Evidence map›Paper›PMID 32881597›Full record

ArticlePharmaceutical biology2020

2,3,5,4'-Tetrahydroxy-stilbene-2-

Lei Yang, Wei Xing, Wang-Zhong Xiao, Lin Tang, Lu Wang, Meng-Jiao Liu, Bing Dai

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

7 authors at 3 institutions in 1 country.

Lei YangDepartment of Preparations, The First Hospital of Hunan University of Chinese Medicine, Changsha, P.R. China.
Wei XingDepartment of Intensive Care Medicine, The Third Xiangya Hospital of Central South University, Changsha, P.R. China.
Wang-Zhong XiaoDepartment of Pharmacy, The First Hospital of Hunan University of Chinese Medicine, Changsha, P.R. China.
Lin TangDepartment of Preparations, The First Hospital of Hunan University of Chinese Medicine, Changsha, P.R. China.
Lu WangDepartment of Preparations, The First Hospital of Hunan University of Chinese Medicine, Changsha, P.R. China.
Meng-Jiao LiuHunan University of Chinese Medicine, Changsha, P.R. China.
Bing DaiDepartment of Pharmacy, The First Hospital of Hunan University of Chinese Medicine, Changsha, P.R. China.ORCID https://orcid.org/0000-0002-7581-6747
First Affiliated Hospital of Hunan University of Traditional Chinese Medicine · CNCentral South University · CNHunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextThe potential hepatotoxicity of

objectiveThis study investigated the specific mechanism by which 2,3,5,4'-tetrahydroxy-stilbene-2- MATERIALS AND

methodsThe toxic effects of TSG (10, 100, 1000 μg/mL) on WRL-68 cells were examined using MTT, flow cytometry, and LDH assay after 24 h of incubation. Untreated cells served as the control. Gene and protein expression levels were determined by quantitative real-time PCR and Western blot, respectively. Immunofluorescence analysis was conducted to investigate the expression of light chain 3 (LC3). Luciferase activity assay was used to assess the targeted regulation of RUNX1 by miR-122.

resultsThe half maximal inhibitory concentration (IC50) of TSG in WRL-68 cells was calculated as 1198.62 μg/mL. TSG (1000 μg/mL) inhibited cell viability and LDH activity and promoted WRL-68 cell apoptosis by inducing autophagy. Subsequent findings showed that TSG induced autophagy and promoted apoptosis in WRL-68 cells by downregulating the levels of p-PI3K, p-Akt, and p-mTOR proteins, while RUNX1 overexpression rescued this inhibition. Additionally, the effect of TSG on hepatocyte apoptosis was reversed by miR-122 knockdown. Furthermore, bioinformatics and dual luciferase reporter assay results indicated that miR-122 targeted RUNX1. DISCUSSION AND

conclusionsOur data demonstrate for the first time that TSG regulates hepatotoxicity, possibly by upregulating miR-122 and inhibiting the RUNX1-mediated PI3K/Akt/mTOR pathway to promote autophagy and induce hepatocyte apoptosis. Further

Indexed as

ApoptosisApoptosis Regulatory ProteinsAutophagyCell LineCell SurvivalChemical and Drug Induced Liver InjuryCore Binding Factor Alpha 2 SubunitGlucosidesHepatocytesHumansMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktStilbenesTOR Serine-Threonine Kinases2,3,5,4'-tetrahydroxystilbene 2-O-glucopyranosideApoptosis Regulatory ProteinsCore Binding Factor Alpha 2 SubunitGlucosidesMicroRNAsMIRN122 microRNA, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRUNX1 protein, humanStilbenesTOR Serine-Threonine Kinasesapoptosis promotionRUNX1TSGWRL-68 cells

Identifiers

PMID32881597
PMCPMC8641687
OpenAlexW3083632014

What OpenQuestion holds

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LicenceCC BY-NC
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.