Evidence map›Paper›PMID 30123297›Full record

ArticleCellular & molecular biology letters2018

Loureirin B inhibits the proliferation of hepatic stellate cells and the Wnt/β-catenin signaling pathway by regulating miR-148-3p.

Jian-Peng Hu, Rong Zhang, Min Tang, Yu-Lian Li, Lin-Ting Xun, Zhi-Zhou Shi, Ying An, Ting Li, Zheng-Ji Song

Open access · goldAbstract read
In one paragraph

Article in Cellular & molecular biology letters, 2018. 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
0.7field-weighted citation impact, top 30% 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, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

9 authors at 2 institutions in 1 country.

Jian-Peng Hu *1Medical School, Kunming University of Science and Technology, Kunming, 650500 Yunnan province China.
Rong Zhang *1Medical School, Kunming University of Science and Technology, Kunming, 650500 Yunnan province China.
Min Tang2Department of Gastroenterology, the First People's Hospital of Yunnan province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032 Yunnan province China.
Yu-Lian Li2Department of Gastroenterology, the First People's Hospital of Yunnan province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032 Yunnan province China.
Lin-Ting Xun2Department of Gastroenterology, the First People's Hospital of Yunnan province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032 Yunnan province China.
Zhi-Zhou Shi1Medical School, Kunming University of Science and Technology, Kunming, 650500 Yunnan province China.
Ying An2Department of Gastroenterology, the First People's Hospital of Yunnan province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032 Yunnan province China.
Ting Li2Department of Gastroenterology, the First People's Hospital of Yunnan province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032 Yunnan province China.
Zheng-Ji Song2Department of Gastroenterology, the First People's Hospital of Yunnan province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032 Yunnan province China.
Kunming University of Science and Technology · CNFirst People's Hospital of Yunnan Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigated the activity of loureirin B against liver fibrosis and the underlying molecular mechanisms.

methodsHepatic stellate cells (HSCs) from Sprague-Dawley rats were treated with different concentrations of loureirin B. We used the MTT assay to determine HSC proliferation, flow cytometry to analyze apoptosis, and western blot to determine the expressions of Bax, Bcl-2, Wnt1 and β-catenin. Real-time PCR was used to determine the expressions of Wnt1 and miR-148-3p.

resultsThe MTT assay showed that loureirin B treatment significantly inhibited the proliferation of HSCs in time- and dose-dependent manners. Loureirin B significantly promoted the apoptosis of HSCs, increased the expression of Bax and decreased the Bcl-2 level. Western blot analysis showed that the expressions of Wnt1 and β-catenin were obviously lower in the loureirin B treatment group than in the control group. We also found that loureirin B could decrease the Wnt1 mRNA level and increase miR-148-3p expression. Knockdown of miR-148-3p using inhibitor could reverse the effects of loureirin B on the proliferation and apoptosis of HSCs and the expressions of Bax, Bcl-2, Wnt1 and β-catenin.

conclusionOur results suggest that loureirin B inhibited the proliferation and promoted the apoptosis of HSCs, and suppressed the Wnt/β-catenin signaling pathway via regulation of miR-148-3p.

Indexed as

AnimalsApoptosisCell ProliferationCells, CulturedGene Expression RegulationHepatic Stellate CellsMaleMicroRNAsRats, Sprague-DawleyResins, PlantWnt Signaling Pathwayloureirin BMicroRNAsMIRN148a microRNA, ratResins, PlantHepatic stellate cellsLiver fibrosisLoureirin BmiR-148-3pWnt1

Identifiers

PMID30123297
PMCPMC6090993
OpenAlexW2885534771

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.