Evidence map›Paper›PMID 33114717›Full record

ReviewInternational journal of molecular sciences2020

Functional Diversity of Non-Histone Chromosomal Protein HmgB1.

Elena Chikhirzhina, Tatyana Starkova, Anton Beljajev, Alexander Polyanichko, Alexey Tomilin

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. HMGB1 as a danger signal in vascular remodeling.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2026
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  17. Structure and Functions of HMGB3 Protein.International journal of molecular sciences · 2024
    Review
  18. Methylation ofJournal of translational internal medicine · 2024
    Article
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Elena ChikhirzhinaInstitute of Cytology of the Russian Academy of Sciences, Laboratory of Molecular Biology of Stem Cells, Tikhoretsky Av. 4, 194064 St. Petersburg, Russia.
Tatyana StarkovaInstitute of Cytology of the Russian Academy of Sciences, Laboratory of Molecular Biology of Stem Cells, Tikhoretsky Av. 4, 194064 St. Petersburg, Russia.ORCID 0000-0001-9708-7808
Anton BeljajevInstitute of Cytology of the Russian Academy of Sciences, Laboratory of Molecular Biology of Stem Cells, Tikhoretsky Av. 4, 194064 St. Petersburg, Russia.
Alexander PolyanichkoInstitute of Cytology of the Russian Academy of Sciences, Laboratory of Molecular Biology of Stem Cells, Tikhoretsky Av. 4, 194064 St. Petersburg, Russia.ORCID 0000-0001-7695-3586
Alexey TomilinInstitute of Cytology of the Russian Academy of Sciences, Laboratory of Molecular Biology of Stem Cells, Tikhoretsky Av. 4, 194064 St. Petersburg, Russia.ORCID 0000-0002-1137-7167
Institute of Cytology · RU

Funding

Russian Foundation for Basic Research 18-04-01199_A, 18-08-01500_A
6 · The paper itself

Abstract

The functioning of DNA in the cell nucleus is ensured by a multitude of proteins, whose interactions with DNA as well as with other proteins lead to the formation of a complicated, organized, and quite dynamic system known as chromatin. This review is devoted to the description of properties and structure of the progenitors of the most abundant non-histone protein of the HMGB family-the HmgB1 protein. The proteins of the HMGB family are also known as "architectural factors" of chromatin, which play an important role in gene expression, transcription, DNA replication, and repair. However, as soon as HmgB1 goes outside the nucleus, it acquires completely different functions, post-translational modifications, and change of its redox state. Despite a lot of evidence of the functional activity of HmgB1, there are still many issues to be solved related to the mechanisms of the influence of HmgB1 on the development and treatment of different diseases-from oncological and cardiovascular diseases to pathologies during pregnancy and childbirth. Here, we describe molecular structure of the HmgB1 protein and discuss general mechanisms of its interactions with other proteins and DNA in cell.

Indexed as

AnimalsCardiovascular DiseasesChromatinDNADNA RepairDNA ReplicationGene Expression RegulationHMGB1 ProteinHumansNeoplasmsProtein Processing, Post-TranslationalTranscription, GeneticChromatinDNAHMGB1 ProteinDNA-proteinextranuclear functions of HmgB1nuclearprotein HmgB1protein–protein interactions

Identifiers

PMID33114717
PMCPMC7662367
OpenAlexW3096443235

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.