Evidence map›Paper›PMID 40612939›Full record

ReviewFrontiers in immunology2025

The role of MCT1 in tumor progression and targeted therapy: a comprehensive review.

Zheng Xu, Xuemei Wang, Hongjing Cheng, Jiuling Li, Xin Zhang, Xueju Wang

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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. GPX8Oncogene · 2026
    Article
  2. Review
  3. Acetate Metabolism in Thyroid Cancer Progression.International journal of molecular sciences · 2026
    Article
  4. Introduction to Cancer Metabolism.Cancer treatment and research · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. 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

6 authors.

Zheng XuDepartment of Pathology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China.
Xuemei WangDepartment of Pathology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China.
Hongjing ChengDepartment of Pathology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China.
Jiuling LiDepartment of Pathology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China.
Xin ZhangDepartment of Pathology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China.
Xueju WangDepartment of Pathology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of monocarboxylate transporter 1 (MCT1) in tumor cells is often associated with poor prognosis. The established mechanisms through which MCT1 and its mediated lactate transport drive tumor progression are manifold. The classical mechanisms include fostering metabolic symbiosis among tumor cells, dampening the immune function of immune cells, and spurring tumor angiogenesis. Beyond these, new findings of MCT1's role in tumor progression have emerged. These new findings highlight MCT1's involvement in mediating the reverse Warburg effect, inhibiting ferroptosis, promoting protective autophagy, and augmenting tumor glycolysis. When acetate serves as a transport substrate for MCT1, additional mechanisms come into play. These encompass MCT1's participation in the acetylation of histone H3K27 and its role in upregulating c-Myc levels. Several studies have demonstrated that while selective MCT1 inhibitors can effectively impede tumor progression, they also face notable challenges. To address these, combining MCT1 inhibitors with other drugs appears to hold more promise.

Indexed as

Monocarboxylic Acid TransportersNeoplasmsSymportersAnimalsDisease ProgressionHumansMolecular Targeted TherapyMonocarboxylate Transport Protein 1Monocarboxylate Transport Protein 1Monocarboxylic Acid TransportersSymportersMCT1MCT1 inhibitoroncogenic mechanismtargeted therapytumor progression

Identifiers

PMID40612939
PMCPMC12222217

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.