Evidence map›Paper›PMID 38657041›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Class IIa HDAC4 and HDAC7 cooperatively regulate gene transcription in Th17 cell differentiation.

Ka Lung Cheung, Li Zhao, Rajal Sharma, Anurupa Abhijit Ghosh, Michael Appiah, Yifei Sun, Anbalagan Jaganathan, Yuan Hu, Alannah LeJeune, Feihong Xu and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Th17 cell pathogenicity in autoimmune disease.Experimental & molecular medicine · 2025
    Review
  8. HDAC7 influences ER-⍺ transcription via NCoR-HDAC3 dissociation.Biochimica et biophysica acta. Proteins and proteomics · 2025
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. 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

18 authors at 2 institutions in 2 countries.

Ka Lung Cheung *Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Li Zhao *Institute of Epigenetic Medicine of the First Hospital, Jilin University, Changchun 130061, China.ORCID 0000-0003-0856-1665
Rajal SharmaDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Anurupa Abhijit GhoshDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0001-7028-9792
Michael AppiahDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Yifei SunDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Anbalagan JaganathanDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Yuan HuDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Alannah LeJeuneDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0003-0822-9777
Feihong XuDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Xinye HanInstitute of Epigenetic Medicine of the First Hospital, Jilin University, Changchun 130061, China.
Xueting WangDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Fan ZhangDepartment of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Chunyan RenDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0002-3913-2479
Martin J WalshDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Huabao XiongDepartment of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0003-0180-2104
Alexander TsankovDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Ming-Ming ZhouDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0002-7049-0573
Icahn School of Medicine at Mount Sinai · USJilin University · CN

Funding

Transcriptional Control of Neuroinflammation in Alzheimer's DiseaseR01AG072562 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAI, DONGMING, ZHOU, MING-MING · 2021 to 2025
$4.2M
Mechanism of BET Proteins in Th17 Cell DifferentiationR01AI124465 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZHOU, MING-MING · 2016 to 2020
$2.9M
Mechanism of Transcriptional Regulation of Th2 Cell DevelopmentR01AI177461 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kalung Cheung, Ming-Ming Zhou · 2023 to 2026
$2.7M
Role of Class IIa HDACs HDAC4 and HDAC7 in Pathogenic Th17 Cell Development and ColitisR01AI168004 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kalung Cheung · 2022 to 2026
$2.5M
Transcriptional Mechanism of BRD4 in Solid TumorR01CA239165 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZHOU, MING-MING · 2019 to 2023
$2.0M
COVID and Translational Science supercomputer (CATS)S10OD030463 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2021 to 2021
$2.0M
Big Omics Data Engine 2 SupercomputerS10OD026880 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2019 to 2019
$2.0M
NCI NIH HHS R01 CA239165NIAID NIH HHS R01 AI124465NIAID NIH HHS R01 AI168004NIAID NIH HHS R01 AI177461NIA NIH HHS R01 AG072562NIH HHS S10 OD026880NIH HHS S10 OD030463
6 · The paper itself

Abstract

Class II histone deacetylases (HDACs) are important in regulation of gene transcription during T cell development. However, our understanding of their cell-specific functions is limited. In this study, we reveal that class IIa Hdac4 and Hdac7 (Hdac4/7) are selectively induced in transcription, guiding the lineage-specific differentiation of mouse T-helper 17 (Th17) cells from naive CD4

Indexed as

Cell DifferentiationColitisHistone DeacetylasesNuclear Receptor Co-Repressor 1Th17 CellsAnimalsGene Expression RegulationHistone Deacetylase 3HumansInterleukin-17Interleukin-2MiceMice, Inbred C57BLNuclear Receptor Co-Repressor 2Repressor ProteinsTranscription FactorsHdac5 protein, mouseHdac7 protein, mouseHistone Deacetylase 3Histone DeacetylasesIl17a protein, mouseInterleukin-17Interleukin-2JunB protein, mouseNcor1 protein, mouseNcor2 protein, mouseNuclear Receptor Co-Repressor 1Nuclear Receptor Co-Repressor 2Repressor ProteinsTranscription Factorsdrug discoverygene transcriptionHDAC4 and HDAC7Th17 cell differentiation

Identifiers

PMID38657041
PMCPMC11067014
OpenAlexW4395111957

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.