Evidence map›Paper›PMID 29527212›Full record

ReviewFrontiers in immunology2018

Targeting Tumor Metabolism: A New Challenge to Improve Immunotherapy.

Soumaya Kouidhi, Farhat Ben Ayed, Amel Benammar Elgaaied

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

123 citing papers in PubMed, 199 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Targeting Lung Cancer Metabolism: Therapeutic Opportunities and Challenges.Advances in experimental medicine and biology · 2026
    Review
  6. Review
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  8. Review
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  10. Article
  11. Review
  12. Article
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  14. Review
  15. Review
  16. RadioFlow Cytometry Reveals That [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  17. Review
  18. The Roles of Myeloid Cells in Breast Cancer Progression.Advances in experimental medicine and biology · 2025
    Review
  19. Association of glutaminase expression with immune-suppressive tumor microenvironment, clinicopathologic features, and clinical outcomes in endometrial cancer.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2024
    Article
  20. Article

63 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Soumaya KouidhiLaboratory BVBGR, LR11ES31, Higher Institute of Biotechnology of Sidi Thabet (ISBST), Department of Biotechnology, University of Manouba, Sidi Thabet, Tunisia.
Farhat Ben AyedAssociation Tunisienne de Lutte contre le Cancer (ATCC), Tunis, Tunisia.
Amel Benammar ElgaaiedLaboratory of Genetics, Immunology and Human Pathology, Faculty of Sciences of Tunis, Department of Biology, University Tunis El Manar, Tunis, Tunisia.
Tunis El Manar University · TNAssociation Tunisienne Contre le Cancer · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, a marked number of clinical trials on cancer treatment have revealed the success of immunomodulatory therapies based on immune checkpoint inhibitors that activate tumor-specific T cells. However, the therapeutic efficacy of cancer immunotherapies is only restricted to a small fraction of patients. A deeper understanding of key mechanisms generating an immunosuppressive tumor microenvironment (TME) remains a major challenge for more effective antitumor immunity. There is a growing evidence that the TME supports inappropriate metabolic reprogramming that dampens T cell function, and therefore impacts the antitumor immune response and tumor progression. Notably, the immunosuppressive TME is characterized by a lack of crucial carbon sources critical for T cell function and increased inhibitory signals. Here, we summarize the basics of intrinsic and extrinsic metabolic remodeling and metabolic checkpoints underlying the competition between cancer and infiltrating immune cells for nutrients and metabolites. Intriguingly, the upregulation of tumor programmed death-L1 and cytotoxic T lymphocyte-associated antigen 4 alters the metabolic programme of T cells and drives their exhaustion. In this context, targeting both tumor and T cell metabolism can beneficially enhance or temper immunity in an inhospitable microenvironment and markedly improve the success of immunotherapies.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, NeoplasmCellular ReprogrammingCostimulatory and Inhibitory T-Cell ReceptorsHumansImmunizationImmunotherapyNeoplasmsT-LymphocytesTumor EscapeTumor MicroenvironmentAntibodies, MonoclonalAntigens, NeoplasmCostimulatory and Inhibitory T-Cell Receptorsimmune checkpointsimmunotherapymetabolic checkpointsT-lymphocyte metabolismtumor cell metabolismtumor microenvironment

Identifiers

PMID29527212
PMCPMC5829092
OpenAlexW2790724421

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.