Evidence map›Paper›PMID 32347025›Full record

ReviewDiabetes & metabolism journal2020

Histone Deacetylase 9: Its Role in the Pathogenesis of Diabetes and Other Chronic Diseases.

Siqi Hu, Eun Hee Cho, Ji Young Lee

Open access · goldAbstract readReview
In one paragraph

Review in Diabetes & metabolism journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

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  18. Proposed minimal essential co-expression and physical interaction networks involved in the development of cognition impairment in human mid and late life.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
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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

3 authors at 2 institutions in 2 countries.

Siqi HuDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT, USA.ORCID 0000-0002-6171-4635
Eun Hee ChoDepartment of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea.
Ji Young LeeDepartment of Nutritional Sciences, University of Connecticut, Storrs, CT, USA. ji-young.lee@uconn.edu.ORCID 0000-0002-7945-793X
University of Connecticut · USKangwon National University · KR

Funding

Nutritional Transcriptomics Approach for the Role of Astaxanthin in Liver FibrosisR01DK108254 · NIDDK · UNIVERSITY OF CONNECTICUT STORRS · PI LEE, JI-YOUNG · 2015 to 2018
$1.5M
NIDDK NIH HHS R01 DK108254NIH HHS 1R01DK108254-01USDA CONS00992
6 · The paper itself

Abstract

As a member of the class IIa histone deacetylases (HDACs), HDAC9 catalyzes the deacetylation of histones and transcription factors, commonly leading to the suppression of gene transcription. The activity of HDAC9 is regulated transcriptionally and post-translationally. HDAC9 is known to play an essential role in regulating myocyte and adipocyte differentiation and cardiac muscle development. Also, recent studies have suggested that HDAC9 is involved in the pathogenesis of chronic diseases, including cardiovascular diseases, osteoporosis, autoimmune disease, cancer, obesity, insulin resistance, and liver fibrosis. HDAC9 modulates the expression of genes related to the pathogenesis of chronic diseases by altering chromatin structure in their promotor region or reducing the transcriptional activity of their respective transcription factors. This review summarizes the current knowledge of the regulation of HDAC9 expression and activity. Also, the roles of HDAC9 in the pathogenesis of chronic diseases are discussed, along with potential underlying mechanisms.

Indexed as

AdipocytesAnimalsAutoimmune DiseasesCardiovascular DiseasesCell DifferentiationChronic DiseaseDiabetes MellitusFemaleHistone DeacetylasesHistonesHumansInsulin ResistanceLiver CirrhosisMiceMuscle CellsNeoplasmsHDAC9 protein, humanHistone DeacetylasesHistonesRepressor ProteinsTranscription FactorsAutoimmune diseasesCardiovascular diseasesChronic diseaseEpigenomicsHistone deacetylasesNeoplasmsObesity

Identifiers

PMID32347025
PMCPMC7188980
OpenAlexW3013825676

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.