Evidence map›Paper›PMID 29402894›Full record

ArticleScientific reports2018

Comprehensive network of miRNA-induced intergenic interactions and a biological role of its core in cancer.

Vladimir V Galatenko, Alexey V Galatenko, Timur R Samatov, Andrey A Turchinovich, Maxim Yu Shkurnikov, Julia A Makarova, Alexander G Tonevitsky

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. MicroRNAs in Genetic Etiology of Human Diseases.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Frontiers in molecular biosciences · 2019
    Article
  18. Review
  19. Deregulated MicroRNA Signature Following Glioblastoma Irradiation.Cancer control : journal of the Moffitt Cancer Center
    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

7 authors at 4 institutions in 4 countries.

Vladimir V GalatenkoLomonosov Moscow State University, Leninskie Gory 1, 119991, Moscow, Russia. vgalat@imscs.msu.ru.ORCID http://orcid.org/0000-0003-3029-3628
Alexey V GalatenkoLomonosov Moscow State University, Leninskie Gory 1, 119991, Moscow, Russia.
Timur R SamatovSRC Bioclinicum, Ugreshskaya str. 2/85, 115088, Moscow, Russia.
Andrey A TurchinovichSciBerg e.Kfm, Birkenauer Str. 7, 68309, Mannheim, Germany.
Maxim Yu ShkurnikovP. Hertsen Moscow Oncology Research Institute, National Center of Medical Radiological Research, Second Botkinsky lane 3, 125284, Moscow, Russia.
Julia A MakarovaP. Hertsen Moscow Oncology Research Institute, National Center of Medical Radiological Research, Second Botkinsky lane 3, 125284, Moscow, Russia.
Alexander G TonevitskySRC Bioclinicum, Ugreshskaya str. 2/85, 115088, Moscow, Russia. tonevitsky@mail.ru.
BioClinicum (Russia) · RULomonosov Moscow State University · RUEngelhardt Institute of Molecular Biology · RUP.A. Hertzen Moscow Oncology Research Institute · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are a family of short noncoding RNAs that posttranscriptionally regulate gene expression and play an important role in multiple cellular processes. A significant percentage of miRNAs are intragenic, which is often functionally related to their host genes playing either antagonistic or synergistic roles. In this study, we constructed and analyzed the entire network of intergenic interactions induced by intragenic miRNAs. We further focused on the core of this network, which was defined as a union of nontrivial strongly connected components, i.e., sets of nodes (genes) mutually connected via directed paths. Both the entire network and its core possessed statistically significant non-random properties. Specifically, genes forming the core had high expression levels and low expression variance. Furthermore, the network core did not split into separate components corresponding to individual signalling or metabolic pathways, but integrated genes involved in key cellular processes, including DNA replication, transcription, protein homeostasis and cell metabolism. We suggest that the network core, consisting of genes mutually regulated by their intragenic miRNAs, could coordinate adjacent pathways or homeostatic control circuits, serving as a horizontal inter-circuit link. Notably, expression patterns of these genes had an efficient prognostic potential for breast and colorectal cancer patients.

Indexed as

Gene Expression Regulation, NeoplasticGene Regulatory NetworksBreast NeoplasmsColorectal NeoplasmsDNA ReplicationFemaleGenes, NeoplasmHumansMetabolic Networks and PathwaysMicroRNAsProteostasisRNA, NeoplasmSurvival AnalysisTranscription, GeneticMicroRNAsRNA, Neoplasm

Identifiers

PMID29402894
PMCPMC5799291
OpenAlexW2786455061

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.