Evidence map›Paper›PMID 31105844›Full record

ArticleAmerican journal of translational research2019

HSC-specific knockdown of GGPPS alleviated CCl

Shan-Shan Lai, Xiao Fu, Qi Cheng, Zi-Han Yu, En-Ze Jiang, Dan-Dan Zhao, De-Cai Yu, Yu-Dong Qiu, Xiang Gao, Huang-Xian Ju and 5 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Fasudil prevents liver fibrosisWorld journal of gastroenterology · 2021
    Article
  8. Review
  9. Article
  10. 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

15 authors at 1 institution in 1 country.

Shan-Shan LaiJiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University Nanjing 210023, China.
Xiao FuJiangsu Key Laboratory of Molecular Medicine and School of Medicine, Nanjing University Nanjing 210093, China.
Qi ChengJiangsu Key Laboratory of Molecular Medicine and School of Medicine, Nanjing University Nanjing 210093, China.
Zi-Han YuJiangsu Key Laboratory of Molecular Medicine and School of Medicine, Nanjing University Nanjing 210093, China.
En-Ze JiangJiangsu Key Laboratory of Molecular Medicine and School of Medicine, Nanjing University Nanjing 210093, China.
Dan-Dan ZhaoJiangsu Key Laboratory of Molecular Medicine and School of Medicine, Nanjing University Nanjing 210093, China.
De-Cai YuDepartment of Hepatobiliary Surgery, The Affiliated Drum Tower Hospital, Medical School of Nanjing University Nanjing 210093, China.
Yu-Dong QiuDepartment of Hepatobiliary Surgery, The Affiliated Drum Tower Hospital, Medical School of Nanjing University Nanjing 210093, China.
Xiang GaoKey Laboratory of Model Animal for Disease Study of Ministry of Education, Model Animal Research Center, Nanjing University Nanjing 210093, China.
Huang-Xian JuMOE Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University Nanjing 210093, China.
Wei WangNational Laboratory of Solid State Microstructures, Department of Physics, Nanjing University Nanjing 210093, China.
Qing JiangDepartment of Sports Medicine and Adult Reconstructive Surgery, Drum Tower Hospital, School of Medicine, Nanjing University Nanjing 210008, China.
Min-Sheng ZhuKey Laboratory of Model Animal for Disease Study of Ministry of Education, Model Animal Research Center, Nanjing University Nanjing 210093, China.
Chao-Jun LiJiangsu Key Laboratory of Molecular Medicine and School of Medicine, Nanjing University Nanjing 210093, China.
Bin XueCore Laboratory, Sir Run Run Hospital, Nanjing Medical University Nanjing 211166, China.
China Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic stellate cells (HSCs) play a critical role in the pathogenesis and reversal of liver fibrosis. Targeting HSCs is of great significance in the treatment of hepatic fibrosis, and has attracted wide attention of scholars. Here we demonstrated that expression of geranylgeranyldiphosphate synthase (GGPPS) predominantly increased in HSCs in murine fibrotic liver. HSC-specific knockdown of GGPPS using vitamin A-coupled liposome carrying siRNA-ggpps decreased activation of HSCs and alleviated fiber accumulation

Indexed as

GGPPShepatic stellate cellliver fibrosisTGF-β1

Identifiers

PMID31105844
PMCPMC6511779
OpenAlexW2981494272

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.