Evidence map›Paper›PMID 28025657›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2017

miR-200a controls hepatic stellate cell activation and fibrosis via SIRT1/Notch1 signal pathway.

Jing-Jing Yang, Hui Tao, Li-Ping Liu, Wei Hu, Zi-Yu Deng, Jun Li

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Acta pharmaceutica Sinica. B · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Circular RNA circUbe2k promotes hepatic fibrosis via sponging miR-149-5p/TGF-β2 axis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  12. Article
  13. Sirtuins at the Service of Healthy Longevity.Frontiers in physiology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Aging, Melatonin, and the Pro- and Anti-Inflammatory Networks.International journal of molecular sciences · 2019
    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

6 authors.

Jing-Jing YangDepartment of Pharmacology, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Hui TaoDepartment of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Li-Ping LiuDepartment of Pharmacology, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Wei HuDepartment of Pharmacology, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Zi-Yu DengDepartment of Scientific, The Second Hospital of Anhui Medical University, Hefei, 230601, China.
Jun LiSchool of Pharmacy, Anhui Medical University, Mei Shan Road, Hefei, Anhui, 230032, China. yncs01@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesmiR-200a has been established as a key regulator of HSC activation processes in liver fibrosis. Epigenetic silencing of miR-200a contributing to SIRT1 over-expression has been discussed in breast cancer; however, whether miR-200a controls SIRT1 gene expression in hepatic fibrosis is still unknown. METHODS AND MATERIALS: We analyzed miR-200a regulation of SIRT1 expression in CCl

resultsWe found that treatment activated HSC with miR-200a mimics, restored miR-200a expression and reduced SIRT1 levels. Conversely, treatment activated HSC with miR-200a inhibitors, decreased miR-200a expression and up-regulated SIRT1 levels. Restoration of miR-200a or the knockdown of SIRT1 prevented HSC activation and proliferation. We have established the SIRT1 transcript as subject to regulation by miR-200a, through miR-200a targeting of SIRT1 3'-UTR. Finally, HSC transfected with SIRT1-siRNA increased the levels of Notch1 protein and mRNA expression.

conclusionsOur study demonstrated that miR-200a regulates SIRT1/Notch1 expression during HSC activation and fibrosis.

Indexed as

AnimalsCell LineCell ProliferationHepatic Stellate CellsLiverLiver CirrhosisMaleMicroRNAsRats, Sprague-DawleyReceptor, Notch1RNA InterferenceSignal TransductionSirtuin 1Transforming Growth Factor beta1MicroRNAsMIRN200 microRNA, ratNotch1 protein, ratReceptor, Notch1Sirt1 protein, ratSirtuin 1Transforming Growth Factor beta1Hepatic stellate cellsLiver fibrosisMicroRNA-200a

Identifiers

What Socratic 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 Socratic graph.