Evidence map›Paper›PMID 28051642›Full record

ArticleCell cycle (Georgetown, Tex.)2016

Early stage of cytomegalovirus infection suppresses host microRNA expression regulation in human fibroblasts.

Anton A Buzdin, Alina V Artcibasova, Natalya F Fedorova, Maria V Suntsova, Andrew V Garazha, Maxim I Sorokin, Daria Allina, Mikhail Shalatonin, Nikolay M Borisov, Alex A Zhavoronkov and 3 more

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. A Review of the Interaction between miRNAs and Ebola Virus.International journal of molecular and cellular medicine · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

13 authors.

Anton A Buzdina Laboratory of Bioinformatics, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology , Moscow , Russia.
Alina V Artcibasovaa Laboratory of Bioinformatics, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology , Moscow , Russia.
Natalya F Fedorovae N.F. Gamaleya Federal Research Centre for Epidemiology and Microbiology of the Ministry of Health of the Russian Federation , Moscow , Russia.
Maria V Suntsovaa Laboratory of Bioinformatics, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology , Moscow , Russia.
Andrew V Garazhaa Laboratory of Bioinformatics, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology , Moscow , Russia.
Maxim I Soroking First Oncology Research and Advisory Center , Moscow , Russia.
Daria Allinaf Moscow Institute of Physics and Technology , Dolgoprudny, Moscow region , Russia.
Mikhail Shalatoninh The Morozov Children's City Hospital , Moscow Russia.
Nikolay M Borisovc National Research Centre "Kurchatov Institute", Centre for Convergence of Nano-, Bio-, Information and Cognitive Sciences and Technologies , Moscow , Russia.
Alex A Zhavoronkova Laboratory of Bioinformatics, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology , Moscow , Russia.
Igor Kovalchuki Department of Biological Sciences , University of Lethbridge , Lethbridge , AB , Canada.
Olga Kovalchuki Department of Biological Sciences , University of Lethbridge , Lethbridge , AB , Canada.
Alla A Kushche N.F. Gamaleya Federal Research Centre for Epidemiology and Microbiology of the Ministry of Health of the Russian Federation , Moscow , Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Responses to human cytomegalovirus (HCMV) infection are largely individual and cell type specific. We investigated molecular profiles in 2 primary cell cultures of human fibroblasts, which are highly or marginally sensitive to HCMV infection, respectively. We screened expression of genes and microRNAs (miRs) at the early (3 hours) stage of infection. To assess molecular pathway activation profiles, we applied bioinformatic algorithms OncoFinder and MiRImpact. In both cell types, pathway regulation properties at mRNA and miR levels were markedly different. Surprisingly, in the infected highly sensitive cells, we observed a "freeze" of miR expression profiles compared to uninfected controls. Our results evidence that in the sensitive cells, HCMV blocks intracellular regulation of microRNA expression already at the earliest stage of infection. These data suggest somewhat new functions for HCMV products and demonstrate dependence of miR expression arrest on the host-encoded factors.

Indexed as

Gene Expression RegulationAdultCell LineCytomegalovirus InfectionsFibroblastsGene Expression ProfilingHumansImmunohistochemistryMicroRNAsReproducibility of ResultsSignal TransductionViral ProteinsMicroRNAsViral ProteinsCytomegalovirus infectiongene transcriptionhuman fibroblastsintracellular signaling pathway regulationmicroRNAtotal miRNAome

Identifiers

PMID28051642
PMCPMC5224468

What OpenQuestion holds

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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.