Evidence map›Paper›PMID 39308084›Full record

ReviewThe FEBS journal2025

Harnessing nucleotide metabolism and immunity in cancer: a tumour microenvironment perspective.

Hadil Suleiman, Alexandra Emerson, Peter M Wilson, Karl A Mulligan, Robert D Ladner, Melissa J LaBonte

Abstract readReview
In one paragraph

Review in The FEBS journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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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.

Hadil SuleimanPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, UK.
Alexandra EmersonPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, UK.
Peter M WilsonCV6 Therapeutics (NI) Ltd, Belfast, UK.
Karl A MulliganCV6 Therapeutics (NI) Ltd, Belfast, UK.
Robert D LadnerPatrick G Johnston Centre for Cancer Research, Queen's University Belfast, UK.
Melissa J LaBontePatrick G Johnston Centre for Cancer Research, Queen's University Belfast, UK.ORCID 0000-0002-0354-413X

Funding

CV6 Therapeutics (NI) LtdExperimental Cancer Medicine Centre (ECMC) C36697/A25176Invest Northern Ireland RDO914247Northern Ireland Department for the Economy
6 · The paper itself

Abstract

The tumour microenvironment (TME) is a dynamic nexus where cancer cell metabolism and the immune system intricately converge, with nucleotide metabolism (NM) playing a pivotal role. This review explores the critical function of NM in cancer cell proliferation and its profound influence on the TME and immune landscape. NM is essential for DNA and RNA synthesis and is markedly upregulated in cancer cells to meet the demands of rapid growth. This metabolic rewiring fuels cancer progression, but also shapes the TME, impacting the function and viability of immune cells. The altered nucleotide milieu in the TME can suppress immune response, aiding cancer cell evasion from immune surveillance. Drug discoveries in the field of NM have revealed different therapeutic strategies, including inhibitors of nucleotide synthesis and drugs targeting salvage pathways, which are discussed thoroughly in this review. Furthermore, the emerging strategy of combining NM-targeted therapies with immunotherapies is emphasised, particularly their effect on sensitising tumours to immune checkpoint inhibitors and enhancing overall treatment efficacy. The Human Genome Project paved the way for personalised medicine, countering the established 'one size fits all' approach to cancer treatment. Advances in understanding the TME and NM have spurred interest in personalised therapeutic strategies. This review highlights the potential of leveraging individual tumour metabolic profiles to guide treatment selection, aiming to optimise efficacy and minimise adverse effects. The strategic importance of targeting NM in cancer therapy and its synergistic potential with immunotherapies offers a path towards more effective and personalised cancer treatments.

Indexed as

NeoplasmsNucleotidesTumor MicroenvironmentAnimalsHumansImmunotherapyNucleotidescancer immunologyimmune checkpoint inhibitorsimmunometabolismmetabolic therapiesnucleotide metabolismpurine metabolismpyrimidine synthesistherapeutic modulationtumour microenvironment

Identifiers

PMID39308084
PMCPMC12062787

What Socratic 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 Socratic graph.