Evidence map›Paper›PMID 32331465›Full record

ReviewPathogens (Basel, Switzerland)2020

Effects of Mycoplasmas on the Host Cell Signaling Pathways.

Sergei N Borchsenius, Innokentii E Vishnyakov, Olga A Chernova, Vladislav M Chernov, Nikolai A Barlev

Open access · goldAbstract readReview
In one paragraph

Review in Pathogens (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Cyclometalated palladium complexes as promising antimycoplasmatic drugs.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Article
  4. Article
  5. Genomic Characterization of aVeterinary sciences · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Toll-Like Receptor 4 ExacerbatesContrast media & molecular imaging · 2022
    Article
  12. The attenuatedFrontiers in microbiology · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Zebrafish · 2021
    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

5 authors at 3 institutions in 1 country.

Sergei N BorchseniusInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.
Innokentii E VishnyakovInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.ORCID 0000-0002-4694-4109
Olga A ChernovaKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center, 420111 Kazan, Russia.
Vladislav M ChernovKazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center, 420111 Kazan, Russia.
Nikolai A BarlevInstitute of Cytology, Russian Academy of Sciences, 194064 St. Petersburg, Russia.
Institute of Cytology · RUKazan Institute of Biochemistry and Biophysics · RUMoscow Institute of Physics and Technology · RU

Funding

Russian Government Programme for the Recruitment of the leading scientists into the Russian Institutions of Higher Education 14.W03.31.0029Russian Science Foundation 17-74-20065Российский Фонд Фундаментальных Исследований (РФФИ) 18-04-00660Российский Фонд Фундаментальных Исследований (РФФИ) 18-29-09144
6 · The paper itself

Abstract

Mycoplasmas are the smallest free-living organisms. Reduced sizes of their genomes put constraints on the ability of these bacteria to live autonomously and make them highly dependent on the nutrients produced by host cells. Importantly, at the organism level, mycoplasmal infections may cause pathological changes to the host, including cancer and severe immunological reactions. At the molecular level, mycoplasmas often activate the NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) inflammatory response and concomitantly inhibit the p53-mediated response, which normally triggers the cell cycle and apoptosis. Thus, mycoplasmal infections may be considered as cancer-associated factors. At the same time, mycoplasmas through their membrane lipoproteins (LAMPs) along with lipoprotein derivatives (lipopeptide MALP-2, macrophage-activating lipopeptide-2) are able to modulate anti-inflammatory responses via nuclear translocation and activation of the Nrf2 (nuclear factor-E2-related anti-inflammatory transcription factor 2). Thus, interactions between mycoplasmas and host cells are multifaceted and depend on the cellular context. In this review, we summarize the current information on the role of mycoplasmas in affecting the host's intracellular signaling mediated by the interactions between transcriptional factors p53, Nrf2, and NF-κB. A better understanding of the mechanisms underlying pathologic processes associated with reprogramming eukaryotic cells that arise during the mycoplasma-host cell interaction should facilitate the development of new therapeutic approaches to treat oncogenic and inflammatory processes.

Indexed as

hemеoxygenase-1 (HO-1)inflammationlipid-associated membrane proteinsmycoplasmaNF-κBNrf2p53post-translational modifications

Identifiers

PMID32331465
PMCPMC7238135
OpenAlexW3019200413

What Socratic holds

Textmetadata
LicenceCC BY
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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.