Evidence map›Paper›PMID 41373684›Full record

ReviewInternational journal of molecular sciences2025

Deaminase Modulation Driving a New Era in Drug Development.

Robyn A Lindley

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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Robyn A LindleyDepartment Clinical Pathology, Victorian Comprehensive Cancer Centre (VCCC), Faculty of Medicine, Dentistry and Health Science, University of Melbourne, Melbourne 3052, Australia.ORCID 0000-0002-8952-1536

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our expanding understanding of the complex roles of endogenous mutagenic deaminases in human disease is driving the development of a new generation of therapeutics. These emerging drugs aim to achieve clinical benefit by modulating deaminase activity. Because these enzymes are intrinsic to key inflammation-related pathways, they represent promising targets for future therapeutic innovation. Although only a small number of deaminase-modulating agents have been approved for clinical use, many more are currently under investigation. Here, we present examples that illustrate the therapeutic potential of modulating this diverse family of enzymes and identify some of the challenges and opportunities that warrant further exploration.

Indexed as

Drug DevelopmentAnimalsHumansInflammationADAR adenosine deaminasesAID cytosine deaminasesAPOBEC cytosine deaminasescancerchronic diseasesdrug developmentendogenous mutagenic deaminasesfunctional modulation and immunotherapyimmunityinflammationprognosticationsmall molecule deaminase inhibitors

Identifiers

PMID41373684
PMCPMC12692628

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.