Evidence map›Paper›PMID 28267418›Full record

ArticleRNA biology2017

MicroRNA-125b-5p mediates post-transcriptional regulation of hepatitis B virus replication via the LIN28B/let-7 axis.

Wanyu Deng, Xiaoyong Zhang, Zhiyong Ma, Yong Lin, Mengji Lu

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.9field-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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. RNAi Regulator C3PO Promotes Arbovirus Infection in Insect Vectors.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Review
  7. Article
  8. Review
  9. Hepatitis B Virus and microRNAs: A Bioinformatics Approach.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
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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

5 authors at 2 institutions in 2 countries.

Wanyu Denga Institute of Virology, University Hospital Essen, University of Duisburg-Essen , Essen , Germany.ORCID 0000-0001-7789-3861
Xiaoyong Zhanga Institute of Virology, University Hospital Essen, University of Duisburg-Essen , Essen , Germany.
Zhiyong Maa Institute of Virology, University Hospital Essen, University of Duisburg-Essen , Essen , Germany.
Yong Lina Institute of Virology, University Hospital Essen, University of Duisburg-Essen , Essen , Germany.ORCID 0000-0001-9171-0195
Mengji Lua Institute of Virology, University Hospital Essen, University of Duisburg-Essen , Essen , Germany.
University of Duisburg-Essen · DEShangrao Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are able to modulate hepatitis B virus (HBV) replication and play an important role in the pathogenesis of HBV infection. Recently, we have identified that serum miR-125b-5p levels correlated with HBV DNA levels and liver necroinflammation. In the present study, we addressed how miR-125b-5p regulated HBV replication at the different steps, inclduing viral transcription, assembly, and virion production and investigated the underlying mechanisms. We found that miR-125b-5p overexpression increased HBV replication without altering HBV transcription. This is the first demonstration of post-transcriptional miRNA regulation of HBV replication. In contrast, transfection of miR-125b-5p inhibitor resulted in downregulation of HBV replication in hepatoma cells. Further, miR-125b-5p inhibited the phosphorylation of retinoblastoma protein and blocked cell cycle progression at the G1/S phase in hepatoma cell lines. Our results indicate that certain miRNAs are able to arrest the cell cycle at G1 phase and may increase HBV replication. RNA sequencing revealed several liver-specific metabolic pathways regulated by miR-125b-5p, which was also found to suppress LIN28B and induce let-7 family members. Additional data demonstrated that miR-125b-5p targeted the LIN28B/let-7 axis to stimulate HBV replication at a post-transcriptional step.

Indexed as

Cell CycleGene Expression RegulationHepatitis BHepatitis B virusHep G2 CellsHumansLiverMetabolic Networks and PathwaysMicroRNAsOrgan SpecificityPhosphorylationRetinoblastoma Binding ProteinsRNA-Binding ProteinsRNA Processing, Post-TranscriptionalSequence Analysis, RNAUbiquitin-Protein LigasesLIN28B protein, humanMicroRNAsMIRN125 microRNA, humanmirnlet7 microRNA, humanRB1 protein, humanRetinoblastoma Binding ProteinsRNA-Binding ProteinsUbiquitin-Protein LigasesHepatitis B virushepatoma cellLIN28BmetabolismmicroRNA

Identifiers

PMID28267418
PMCPMC5711457
OpenAlexW2592188106

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.