Evidence map›Paper›PMID 42827624›Full record

ReviewFrontiers in cell and developmental biology2026

PFKP in malignant tumors: bridging metabolic reprogramming, post-translational modifications, and the immunosuppressive microenvironment.

Jing-Jing Zhao, Gangyuan Ma, Rui Zong, Jinlan Zhong, Yicheng Zhao, Liang Liu, Runze Li

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jing-Jing Zhao *Chinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.
Gangyuan Ma *Chinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.
Rui Zong *Chinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.
Jinlan Zhong *Chinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.
Yicheng ZhaoChinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.
Liang LiuChinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.
Runze LiChinese Medicine Guangdong Laboratory/State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Clinical College, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic reprogramming is a hallmark of malignant tumors. Platelet-type phosphofructokinase (PFKP), a rate-limiting enzyme in glycolysis, is aberrantly overexpressed across diverse cancers and promotes tumor proliferation, invasion, and metastasis through both metabolic and non-metabolic pathways. The enzymatic activity, stability, and subcellular localization of PFKP are dynamically regulated by post-translational modifications-including phosphorylation, ubiquitination, acetylation, and lactylation-as well as by protein-protein interaction networks. Upon nuclear translocation, PFKP dissociates from glycolytic flux and engages in oncogenic transcriptional regulation. Moreover, PFKP upregulates PD-L1 expression, alters chemokine profiles, disrupts immune cell infiltration, and fosters an immunosuppressive microenvironment that facilitates immune evasion. Emerging evidence suggests PFKP holds diagnostic and prognostic potential, yet direct targeting evidence remains lacking, and most inhibitor studies are confined to preclinical models. This review synthesizes recent advances in PFKP research, focusing on its regulatory networks in tumor metabolism, post-translational modifications, protein interactions, and immune remodeling. We critically evaluate current controversies, unresolved questions, and translational barriers, and propose future directions-including epigenetic regulation, functional characterization of interacting partners, and combination strategies with immunotherapy-to inform precision oncology and targeted therapeutic development.

Indexed as

glycolysismetabolic reprogrammingPFKPpost-translational modificationtumor immune evasiontumor microenvironment

Identifiers

PMID42827624
PMCPMC13631397

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.