Evidence map›Paper›PMID 29781349›Full record

ReviewExpert opinion on therapeutic targets2018

Recent advances in targeting protein arginine methyltransferase enzymes in cancer therapy.

Emily Smith, Wei Zhou, Polina Shindiapina, Said Sif, Chenglong Li, Robert A Baiocchi

Open access · bronzeAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 78 citations in OpenAlex.

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  7. PRMT3 and CARM1: Emerging Epigenetic Targets in Cancer.Journal of cellular and molecular medicine · 2025
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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

6 authors at 3 institutions in 2 countries.

Emily Smitha The Division of Hematology, Department of Internal Medicine , The Ohio State University , Columbus , OH , USA.
Wei Zhoub Department of Biochemistry and Molecular Biology, College of Medicine , University of Florida , Gainesville , FL , USA.ORCID 0000-0003-3895-1429
Polina Shindiapinaa The Division of Hematology, Department of Internal Medicine , The Ohio State University , Columbus , OH , USA.
Said Sifd Department of Biological and Environmental Sciences, College of Arts and Sciences , Qatar University , Doha , Qatar.
Chenglong Lib Department of Biochemistry and Molecular Biology, College of Medicine , University of Florida , Gainesville , FL , USA.
Robert A Baiocchia The Division of Hematology, Department of Internal Medicine , The Ohio State University , Columbus , OH , USA.
The Ohio State University · USUniversity of Florida · USQatar University · QA

Funding

ONOCOLOGY TRAINING GRANTT32CA009338 · NCI · OHIO STATE UNIVERSITY · PI BYRD, JOHN C., POLLOCK, RAPHAEL E. · 1985 to 2018
$8.3M
Targeted Therapies for Richters TransformationR01CA214046 · NCI · OHIO STATE UNIVERSITY · PI BAIOCCHI, ROBERT ALAN, BYRD, JOHN C. · 2017 to 2021
$2.3M
NCI NIH HHS R01 CA214046NCI NIH HHS T32 CA009338
6 · The paper itself

Abstract

introductionExploration in the field of epigenetics has revealed the diverse roles of the protein arginine methyltransferase (PRMT) family of proteins in multiple disease states. These findings have led to the development of specific inhibitors and discovery of several new classes of drugs with potential to treat both benign and malignant conditions. Areas covered: We provide an overview on the role of PRMT enzymes in healthy and malignant cells, highlighting the role of arginine methylation in specific pathways relevant to cancer pathogenesis. Additionally, we describe structure and catalytic activity of PRMT and discuss the mechanisms of action of novel small molecule inhibitors of specific members of the arginine methyltransferase family. Expert opinion: As the field of PRMT biology advances, it's becoming clear that this class of enzymes is highly relevant to maintaining normal physiologic processes as well and disease pathogenesis. We discuss the potential impact of PRMT inhibitors as a broad class of drugs, including the pleiotropic effects, off target effects the need for more detailed PRMT-centric interactomes, and finally, the potential for targeting this class of enzymes in clinical development of experimental therapeutics for cancer.

Indexed as

AnimalsAntineoplastic AgentsDrug DesignDrug DiscoveryEnzyme InhibitorsEpigenesis, GeneticHumansMolecular Targeted TherapyNeoplasmsProtein-Arginine N-MethyltransferasesAntineoplastic AgentsEnzyme InhibitorsProtein-Arginine N-Methyltransferasesarginine-methylationCancerepigeneticstherapeutic target

Identifiers

PMID29781349
PMCPMC6311705
OpenAlexW2803197392

What OpenQuestion holds

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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.