Evidence map›Paper›PMID 40567251›Full record

ReviewMedComm2025

Glutamine Metabolism: Molecular Regulation, Biological Functions, and Diseases.

Mudasir A Kumar, Sana Khurshid Baba, Inamu Rashid Khan, Mohd Shahnawaz Khan, Fohad Mabood Husain, Saheem Ahmad, Mohammad Haris, Mayank Singh, Ammira S Al-Shabeeb Akil, Muzafar A Macha and 1 more

Abstract readReview
In one paragraph

Review in MedComm, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. SFRP2Molecular carcinogenesis · 2026
    Article
  2. Review
  3. High-Density Type I Collagen Promotes IFN-γAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Injury Causes Altered Metabolism including ObioRxiv : the preprint server for biology · 2026
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review
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

11 authors.

Mudasir A KumarWatson-Crick Centre for Molecular Medicine Islamic University of Science and Technology Kashmir India.
Sana Khurshid BabaWatson-Crick Centre for Molecular Medicine Islamic University of Science and Technology Kashmir India.
Inamu Rashid KhanDepartment of Zoology School of Life Sciences Central University of Kashmir Ganderbal India.
Mohd Shahnawaz KhanDepartment of Biochemistry College of Sciences King Saud University Riyadh Saudi Arabia.
Fohad Mabood HusainDepartment of Food Science and Nutrition College of Food and Agriculture Sciences King Saud University Riyadh Saudi Arabia.
Saheem AhmadDepartment of Medical Laboratory Sciences College of Applied Medical Sciences University of Hail Hail City Saudi Arabia.
Mohammad HarisCenter for Advanced Metabolic Imaging in Precision Medicine Department of Radiology Perelman School of Medicine University of Pennsylvania Philadelphia USA.
Mayank SinghDepartment of Medical Oncology (Lab.) Dr. BRAIRCH All India Institute of Medical Sciences (AIIMS) New Delhi India.
Ammira S Al-Shabeeb AkilDepartment of Human Genetics-Precision Medicine in Diabetes Obesity and Cancer Program, Sidra Medicine Doha Qatar.
Muzafar A MachaWatson-Crick Centre for Molecular Medicine Islamic University of Science and Technology Kashmir India.ORCID https://orcid.org/0000-0003-4468-4435
Ajaz A BhatDepartment of Human Genetics-Precision Medicine in Diabetes Obesity and Cancer Program, Sidra Medicine Doha Qatar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glutaminolysis, the metabolic process of converting glutamine into key intermediates, plays an essential role in cellular energy production, signaling, biosynthesis, and redox balance. Deregulation of glutamine metabolism significantly influences various pathological conditions, including cancers and metabolic and neurological diseases. Emerging evidence shows that long noncoding RNAs (lncRNAs), circular RNAs (circRNAs), and oncogenic alterations in glutamine transporters and enzymes enhance glutamine's role as an alternative energy source, supporting cell survival and proliferation under nutrient and oxygen deprivation conditions. To combat the pathogenic effects of altered glutamine metabolism, researchers are developing targeted inhibitors of key enzymes and transporters involved in glutaminolysis. By interfering with the mechanisms that support the growth of cancer cells, these inhibitors may be able to stop the growth of tumors and treat metabolic and neurological conditions. This review provides a comprehensive overview of existing inhibitors and ongoing clinical trials targeting glutamine metabolism, focusing on its potential as a cancer therapeutic strategy. Additionally, the role of lncRNAs and circRNAs in regulating glutamine metabolism is explored, revealing novel avenues for therapeutic intervention in cancer and other diseases.

Indexed as

cancercircular RNAsglutamine metabolismglutaminolysislong noncoding RNAstherapeutic targeting

Identifiers

PMID40567251
PMCPMC12188105

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.