Evidence map›Paper›PMID 39584783›Full record

SynthesisGenes, chromosomes & cancer2024

Aberrant Energy Metabolism in Tumors and Potential Therapeutic Targets.

Shuhao Fan, Jianhua Guo, Hui Nie, Huabao Xiong, Yong Xia

Abstract readSystematic Review
In one paragraph

Synthesis in Genes, chromosomes & cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. A bezafibrate bearing Pt(IV) prodrug triggers ferroptosis via modulating lipid metabolism in lung cancer cells.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2026
    Article
  5. Acetate Metabolism in Thyroid Cancer Progression.International journal of molecular sciences · 2026
    Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. AhR and STAT3: A Dangerous Duo in Chemical Carcinogenesis.International journal of molecular sciences · 2025
    Review
  11. Article
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

5 authors.

Shuhao FanShandong First Medical University, Jinan, Shandong, People's Republic of China.
Jianhua GuoCollege of Medical Engineering, Jining Medical University, Jining, Shandong, People's Republic of China.
Hui NieShandong First Medical University, Jinan, Shandong, People's Republic of China.
Huabao XiongInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, Shandong, People's Republic of China.
Yong XiaShandong First Medical University, Jinan, Shandong, People's Republic of China.ORCID 0000-0002-1020-0263

Funding

Co-construction of Science and Technology Projects by the Science and Technology Department of the State Administration of Traditional Chinese Medicine G2Y-kJS-SD-2023-097National Natural Science Foundation of China 82372674Natural Science Foundation of Shandong Province ZR2023LZL005Taishan Scholars Program of Shandong Province tsqn201909147
6 · The paper itself

Abstract

Energy metabolic reprogramming is frequently observed during tumor progression as tumor cells necessitate adequate energy production for rapid proliferation. Although current medical research shows promising prospects in studying the characteristics of tumor energy metabolism and developing anti-tumor drugs targeting energy metabolism, there is a lack of systematic compendiums and comprehensive reviews in this field. The objective of this study is to conduct a systematic review on the characteristics of tumor cells' energy metabolism, with a specific focus on comparing abnormalities between tumor and normal cells, as well as summarizing potential targets for tumor therapy. Additionally, this review also elucidates the aberrant mechanisms underlying four major energy metabolic pathways (glucose, lipid, glutamine, and mitochondria-dependent) during carcinogenesis and tumor progression. Through the utilization of graphical representations, we have identified anomalies in crucial energy metabolism pathways, encompassing transporter proteins (glucose transporter, CD36, and ASCT2), signaling molecules (Ras, AMPK, and PTEN), as well as transcription factors (Myc, HIF-1α, CREB-1, and p53). The key molecules responsible for aberrant energy metabolism in tumors may serve as potential targets for cancer therapy. Therefore, this review provides an overview of the distinct energy-generating pathways within tumor cells, laying the groundwork for developing innovative strategies for precise cancer treatment.

Indexed as

Energy MetabolismNeoplasmsAnimalsGlucoseHumansMolecular Targeted TherapySignal TransductionGlucoseenergy metabolism abnormalityglucose metabolismglutamine metabolismlipid metabolismoxidative phosphorylation

Identifiers

PMID39584783
PMCPMC11587691

What OpenQuestion holds

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Registered trials

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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.