Evidence map›Paper›PMID 40869229›Full record

ReviewInternational journal of molecular sciences2025

Current and Emerging Therapies for Targeting Protein Arginine Methyltransferases (PRMTs) in Cancer.

Adriana Kaganovski, Bayle Smith-Salzberg, Hadar K Shimshon, Andrew Draheim, Mark Spivak, Tzuriel Sapir, David Shifteh

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Special Issue "Protein Methyltransferases in Human Health and Diseases".International journal of molecular sciences · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. A Further Case for Targeting PRMT5 and the ERK1/2 and PI3K Pathways in CRC.International journal of molecular sciences · 2025
    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.

Adriana KaganovskiCollege of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.
Bayle Smith-SalzbergCollege of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.
Hadar K ShimshonCollege of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.
Andrew DraheimCollege of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.
Mark SpivakCollege of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.
Tzuriel SapirPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-1689-2176
David ShiftehCollege of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.ORCID 0000-0002-4108-4664

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein arginine methyltransferases (PRMTs) are a class of enzymes that mediate critical post-translational modifications through arginine methylation as epigenetic regulators. PRMTs have been shown to have a vast array of regulatory effects including in gene expression, signal transduction, and cellular proliferation. Dysregulation of PRMT activity has been seen in the progression of various cancers, including breast, lung, and colorectal cancer. Moreover, PRMT overexpression has been shown to correlate with poor patient prognosis. This review aims to explore the roles of the individual PRMTs in cancer and aims to highlight the latest and newest developments of PRMT inhibitors as emerging therapeutic strategies. Numerous preclinical and clinical studies have identified several novel compounds that effectively target PRMT activity and have shown significant therapeutic results. As such, this review aims to not only highlight the current research findings, but to also emphasize the significant need for future research on PRMTs as novel therapeutic targets in cancer.

Indexed as

Antineoplastic AgentsEnzyme InhibitorsNeoplasmsProtein-Arginine N-MethyltransferasesAnimalsEpigenesis, GeneticHumansMethylationMolecular Targeted TherapyProtein Processing, Post-TranslationalAntineoplastic AgentsEnzyme InhibitorsProtein-Arginine N-MethyltransferasesPRMTPRMT1PRMT2PRMT3PRMT4PRMT5PRMT6PRMT7PRMT8PRMT9

Identifiers

PMID40869229
PMCPMC12386604

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.