Evidence map›Paper›PMID 32174788›Full record

ArticleInternational journal of biological sciences2020

C-terminal binding proteins 1 and 2 in traumatic brain injury-induced inflammation and their inhibition as an approach for anti-inflammatory treatment.

Hong Li, Caiguo Zhang, Chunxia Yang, Melanie Blevins, David Norris, Rui Zhao, Mingxia Huang

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. 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

7 authors at 2 institutions in 2 countries.

Hong LiDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
Caiguo ZhangDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
Chunxia YangDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
Melanie BlevinsDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
David NorrisDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
Rui ZhaoDepartment of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
Mingxia HuangDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora CO 80045, USA.
University of Colorado Anschutz Medical Campus · USFirst Hospital of Shanxi Medical University · CN

Funding

Training in Translational Research of Lung, Head and Neck CancerT32CA174648 · NCI · UNIVERSITY OF COLORADO DENVER · PI KARAM, SANA D · 2013 to 2022
$4.2M
Role of Eya3 in regulating the immune microenvironment to promote breast tumor progressionR01CA221282 · NCI · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L., ZHAO, RUI · 2017 to 2021
$3.2M
Understanding the structure and function of U1 snRNPR01GM126157 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI ZHAO, RUI · 2018 to 2021
$1.8M
Structure and function of U5 snRNPR01GM114178 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI ZHAO, RUI · 2015 to 2018
$1.4M
BLRD VA I01 BX002370NCI NIH HHS R01 CA221282NCI NIH HHS T32 CA174648NIGMS NIH HHS R01 GM114178NIGMS NIH HHS R01 GM126157
6 · The paper itself

Abstract

Traumatic brain injury (TBI) induces an acute inflammatory response in the central nervous system that involves both resident and peripheral immune cells. The ensuing chronic neuroinflammation causes cell death and tissue damage and may contribute to neurodegeneration. The molecular mechanisms involved in the maintenance of this chronic inflammation state remain underexplored. C-terminal binding protein (CtBP) 1 and 2 are transcriptional coregulators that repress diverse cellular processes. Unexpectedly, we find that the CtBPs can transactivate a common set of proinflammatory genes both in lipopolysaccharide-activated microglia, astrocytes and macrophages, and in a mouse model of the mild form of TBI. We also find that the expression of these genes is markedly enhanced by a single mild injury in both brain and peripheral blood leukocytes in a severity- and time-dependent manner. Moreover, we were able to demonstrate that specific inhibitors of the CtBPs effectively suppress the expression of the CtBP target genes and thus improve neurological outcome in mice receiving single and repeated mild TBIs. This discovery suggests new avenues for therapeutic modulation of the inflammatory response to brain injury.

Indexed as

Alcohol OxidoreductasesAnimalsAnti-Inflammatory AgentsAstrocytesBrain Injuries, TraumaticCo-Repressor ProteinsDNA-Binding ProteinsInflammationMacrophagesMiceMice, Inbred C57BLMicrogliaAlcohol OxidoreductasesAnti-Inflammatory AgentsCo-Repressor ProteinsCtbp2 protein, mouseC-terminal binding proteinDNA-Binding ProteinsCtBPmicroglia activationneuroinflammationproinflammatory transcriptiontraumatic brain injury

Identifiers

PMID32174788
PMCPMC7053329
OpenAlexW3006472243

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.