Evidence map›Paper›PMID 41169372›Full record

ReviewFrontiers in immunology2025

Targeting PKM2 in cancer therapeutics: mechanistic advances and translational opportunities.

Lin Liu, Junyi Wang, Libo Liang, Chunhua Chen, Meng Xie, Wencheng Tang

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Recent progress in small molecules targeting the acidic tumor microenvironment.Journal of enzyme inhibition and medicinal chemistry · 2026
    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.

Lin LiuDrug Dispending Department, The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang, China.
Junyi WangDrug Dispending Department, The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang, China.
Libo LiangDrug Dispending Department, The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang, China.
Chunhua ChenDrug Dispending Department, The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang, China.
Meng XieDrug Dispending Department, The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang, China.
Wencheng TangDrug Dispending Department, The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

M2-type pyruvate kinase (PKM2) serves as the key rate-limiting enzyme in aerobic glycolysis within tumor cells, where its aberrantly high expression in numerous human malignancies facilitates tumor progression by enhancing glycolytic flux through diverse signaling pathways. Beyond its metabolic function, extensive studies have established PKM2 as a critical non-metabolic signaling regulator implicated in multiple oncogenic processes, including tumor proliferation, invasion, migration, immune evasion, and resistance to chemotherapy. The elucidation of PKM2-mediated oncogenic pathways has spurred the development of targeted therapeutic strategies, positioning PKM2 as a promising target in cancer therapy. However, comprehensive reviews addressing the relationship between PKM2 and tumorigenesis remain limited. This review systematically examines the biological functions of PKM2, the signaling mechanisms through which it exerts its effects in malignant tumors, and the latest advances in the development of PKM2-targeted therapeutics, offering insights into potential directions for future drug discovery.

Indexed as

Antineoplastic AgentsCarrier ProteinsMembrane ProteinsNeoplasmsPyruvate KinaseThyroid HormonesAnimalsGlycolysisHumansMolecular Targeted TherapySignal TransductionThyroid Hormone-Binding ProteinsAntineoplastic AgentsCarrier ProteinsMembrane ProteinsPyruvate KinaseThyroid Hormone-Binding ProteinsThyroid Hormonesaerobic glycolysisanti-cancerM2-type pyruvate kinasePKM2-targeted therapeuticssignaling networks

Identifiers

PMID41169372
PMCPMC12568514

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.