Evidence map›Paper›PMID 32888819›Full record

ReviewTrends in immunology2020

Protein Arginine Methyltransferase 5 in T Lymphocyte Biology.

Shouvonik Sengupta, Austin Kennemer, Kristin Patrick, Philip Tsichlis, Mireia Guerau-de-Arellano

Open access · greenAbstract readReview
In one paragraph

Review in Trends in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  4. Enhancing CD8Biomolecules · 2025
    Article
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  7. Review
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  13. Review
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  17. Review
  18. Article
  19. Article
  20. The Role of Protein Arginine Methyltransferases in DNA Damage Response.International journal of molecular sciences · 2022
    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 3 institutions in 1 country.

Shouvonik SenguptaSchool of Health and Rehabilitation Sciences, Division of Medical Laboratory Science, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA; Biomedical Sciences Graduate Program, The Ohio State University, Columbus, OH, USA.
Austin KennemerSchool of Health and Rehabilitation Sciences, Division of Medical Laboratory Science, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Kristin PatrickDepartment of Microbial Pathogenesis and Immunology, Texas A&M Health Science Center, Bryan, TX, USA.
Philip TsichlisDepartment of Cancer Biology and Genetics, The Ohio State University, Columbus, Ohio, USA; The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Mireia Guerau-de-ArellanoSchool of Health and Rehabilitation Sciences, Division of Medical Laboratory Science, College of Medicine, Wexner Medical Center, The Ohio State University, Columbus, OH, USA; Institute for Behavioral Medicine Research, The Ohio State University, Columbus, OH, USA; Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, USA; Department of Neuroscience, The Ohio State University, Columbus, OH, USA; The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA. Electronic address: mireia.guerau@osumc.edu.
The Ohio State University Wexner Medical Center · USTexas A&M Health Science Center · USThe Ohio State University · US

Funding

Epigenetic modulation of T cell tolerance in Multiple Sclerosis autoimmunityR01AI121405 · NIAID · OHIO STATE UNIVERSITY · PI GUERAU-DE-ARELLANO, MIREIA · 2016 to 2020
$2.2M
Differential Regulation of RNA processing by Akt isoformsR01CA186729 · NCI · TUFTS MEDICAL CENTER · PI TSICHLIS, PHILIP N. · 2015 to 2019
$1.8M
Novel Epigenetic Modifier Inhibitor Drugs for T cell Modulation in Multiple SclerosisR21AI127354 · NIAID · OHIO STATE UNIVERSITY · PI GUERAU-DE-ARELLANO, MIREIA · 2017 to 2018
$404k
Novel knockout models to analyze CD38 functionR03AI151769 · NIAID · OHIO STATE UNIVERSITY · PI GUERAU-DE-ARELLANO, MIREIA · 2020 to 2021
$156k
NCI NIH HHS R01 CA186729NIAID NIH HHS R01 AI121405NIAID NIH HHS R03 AI151769NIAID NIH HHS R21 AI127354
6 · The paper itself

Abstract

Protein arginine methyltransferase 5 (PRMT5) is the major methyltransferase (MT) catalyzing symmetric dimethylation (SDM). PRMT5 regulates developmental, homeostatic and disease processes in vertebrates and invertebrates, and a carcinogenic role has been observed in mammals. Recently, tools generated for PRMT5 loss of function have allowed researchers to demonstrate essential roles for PRMT5 in mouse and human lymphocyte biology. PRMT5 modulates CD4

Indexed as

Cell DifferentiationProtein-Arginine N-MethyltransferasesTh17 CellsT-LymphocytesAnimalsHumansProtein-Arginine N-Methyltransferasesarginine methylationautoimmunitylymphocytesPRMT5

Identifiers

PMID32888819
PMCPMC9425078
OpenAlexW3081906934

What OpenQuestion holds

Textmetadata
LicenceTDM
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.