Evidence map›Paper›PMID 28864162›Full record

ArticleEBioMedicine2017

Treatment-Induced Viral Cure of Hepatitis C Virus-Infected Patients Involves a Dynamic Interplay among three Important Molecular Players in Lipid Homeostasis: Circulating microRNA (miR)-24, miR-223, and Proprotein Convertase Subtilisin/Kexin Type 9.

Anastasia Hyrina, Andrea D Olmstead, Paul Steven, Mel Krajden, Edward Tam, François Jean

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Epigenetic Mechanisms Involved in Hcv Infection and Human HCC.International journal of molecular sciences · 2025
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  4. Article
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  7. Article
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  9. The Multifaceted Biology of PCSK9.Endocrine reviews · 2022
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  13. 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

6 authors at 4 institutions in 2 countries.

Anastasia HyrinaDept. of Microbiology and Immunology, University of British Columbia, Canada. Electronic address: ahyrina@mail.ubc.ca.
Andrea D OlmsteadDept. of Microbiology and Immunology, University of British Columbia, Canada. Electronic address: Andrea.Olmstead@bccdc.ca.
Paul StevenQIAGEN, United Kingdom. Electronic address: paul.steven@qiagen.com.
Mel KrajdenBCCDC Public Health Microbiology and Reference Laboratory, Canada. Electronic address: Mel.Krajden@bccdc.ca.
Edward TamLAIR Centre, Canada. Electronic address: etam@laircentre.com.
François JeanDept. of Microbiology and Immunology, University of British Columbia, Canada. Electronic address: fjean@mail.ubc.ca.
University of British Columbia · CABC Centre for Disease Control · CAPrairie Women's Health Centre of Excellence · CAQiagen (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In patients with chronic hepatitis C virus (HCV) infection, viral hijacking of the host-cell biosynthetic pathways is associated with altered lipid metabolism, which contributes to disease progression and may influence antiviral response. We investigated the molecular interplay among four key regulators of lipid homeostasis [microRNA (miR)-122, miR-24, miR-223, and proprotein convertase subtilisin/kexin type 9 (PCSK9)] in HCV-infected patients (n=72) who achieved a treatment-based viral cure after interferon-based therapy with first-generation direct-acting antivirals. Real-time PCR was used to quantify microRNA plasma levels, and ELISA assays were used to determine plasma concentrations of PCSK9. We report that levels of miR-24 and miR-223 significantly increased in patients achieving sustained virologic response (SVR), whereas the levels of miR-122, a liver-specific cofactor for HCV infection, decreased in these patients. PCSK9 concentrations were significantly increased in SVRs, suggesting that PCSK9 may help impede viral infection. The modulatory effect of PCSK9 on HCV infection was also demonstrated in the context of HCV-infected Huh-7.5.1 cells employing recombinant human PCSK9 mutants. Together, these results provide insights into a novel coordinated interplay among three important molecular players in lipid homeostasis - circulating miR-24, miR-223 and PCSK9 - whose regulation is affected by HCV infection and treatment-based viral cure.

Indexed as

HepacivirusHomeostasisLipid MetabolismAnalysis of VarianceAntiviral AgentsBiomarkersCell LineCells, CulturedCirculating MicroRNAEnzyme-Linked Immunosorbent AssayFemaleGenotypeHepatitis CHepatitis C, ChronicHumansMaleAntiviral AgentsBiomarkersCirculating MicroRNALDLR protein, humanMicroRNAsMIR223, humanMIRN24 microRNA, humanPCSK9 protein, humanProprotein Convertase 9Receptors, LDLAntiviral therapyHepatitis C virusmiR-122miR-223miR-24Proprotein convertase subtilisin/kexin type 9

Identifiers

PMID28864162
PMCPMC5605363
OpenAlexW2747011695

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.