| 2021 |
ZEB1 directly activates PFKM transcription through a non-classic ZEB1-binding sequence in the PFKM promoter region, upregulating PFKM expression and glycolysis in HCC cells; silencing ZEB1 impairs PFKM expression, glycolysis, proliferation and invasion, and exogenous PFKM re-expression rescues these defects. |
shRNA knockdown, ChIP assay, luciferase reporter assay, RT-qPCR, Western blot, ECAR/OCR assays, orthotopic xenograft |
Theranostics |
High |
33897890
|
| 2020 |
Mycobacterium tuberculosis-induced miR-21 directly targets PFKM mRNA to repress its expression and activity in macrophages, dampening glycolysis and limiting IL-1β production; IFN-γ inhibits miR-21, forcing an isoenzyme switch that augments PFKM expression and macrophage glycolysis. |
miRNA target validation, PFK isoenzyme activity assays, miR-21 manipulation in macrophages, cytokine measurement |
Cell reports |
High |
31914380
|
| 2021 |
NOS1 S-nitrosylates PFKM at Cys351, stabilizing the PFKM tetramer and enabling resistance to negative feedback from downstream metabolic intermediates, thereby promoting glycolysis in ovarian cancer cells; PFKM-C351S mutation reduced proliferation and tumor growth in xenograft models. |
S-nitrosoproteomic profiling, site-directed mutagenesis (C351S), in vitro tetramer stability assay, xenograft tumor model |
Cell death & disease |
High |
33859186
|
| 2025 |
Citrate binds PFKM and disrupts its tetrameric structure into dimers; dimeric PFKM interacts with nucleosomes and phosphorylates histone H3 at serine 10 (H3S10) as a protein kinase, promoting mitotic progression and cell proliferation. Structural simulations show PFKM binds nucleosomes optimally when H3S10 aligns with its catalytic site. |
Structural simulation, biochemical citrate-binding assays, in vitro histone kinase assay, mutagenesis disrupting citrate-PFKM and PFKM-H3 interactions, cell cycle analysis, tumor growth assays |
Nature communications |
High |
40695785
|
| 2025 |
Wnt signalling induces lysosomal degradation of PFKM through a methyl arginine degron motif that is selectively methylated by PRMT1, delivering PFKM to lysosomes via microautophagy; PFKM degradation shifts glucose metabolism from glycolysis to the pentose phosphate pathway, and PFKM overexpression promotes myofibre differentiation while PFKM knockdown blunts differentiation (rescued by 3-phosphoglycerate supplementation). |
Genetic knockdown/overexpression, metabolic flux analysis, PRMT1-mediated methylation validation, lysosomal inhibition experiments, metabolic rescue with 3-phosphoglycerate |
Nature metabolism |
High |
41735679
|
| 2024 |
METTL16 mediates m6A methylation to stabilize PFKM mRNA in an IGF2BP3-dependent manner in HCC, promoting glycolysis; POU3F2 transcriptionally activates METTL16, defining a POU3F2/METTL16/PFKM axis. |
MeRIP assay, RIP assay, actinomycin D mRNA stability assay, ChIP, luciferase assay, knockdown/overexpression, xenograft |
Annals of hepatology |
Medium |
39756795
|
| 2024 |
NAT10-mediated ac4C acetylation suppresses m6A modification on PFKM mRNA; YTHDC1 recognizes m6A sites on PFKM mRNA to increase its stability; NAT10 knockdown increases m6A content, reducing YTHDC1 translation, and destabilizing PFKM mRNA, leading to decreased glycolysis in osteosarcoma cells. |
NAT10 knockdown, m6A-seq, RIP assay, m6A reader protein analysis, mRNA stability assay, in vivo tumor models |
Cell communication and signaling |
Medium |
38233839
|
| 2024 |
HIF-1α increases METTL3 expression, which elevates m6A modification on Pfkm mRNA and upregulates PFKM protein expression in macrophages; recombinant thrombomodulin (rTM) decreases PFKM expression in a HIF-1α-dependent manner, and METTL3 silencing attenuates HIF-1α-mediated PFKM upregulation. |
HIF-1α overexpression/knockdown, METTL3 silencing, m6A quantification, Pfkm knockout mice, ELISA cytokine measurement |
Cellular and molecular life sciences |
Medium |
39549085
|
| 2024 |
USP35 deubiquitinates and stabilizes PFK-1 (PFKM) protein; Co-IP identified PFK-1 as a direct deubiquitination target of USP35, and USP35 knockdown decreased PFK-1 expression, reducing glycolysis and cancer cell proliferation. |
Co-immunoprecipitation, immunoprecipitation/ubiquitination assay, USP35 knockdown, Seahorse glycolysis assay, xenograft |
American journal of physiology. Cell physiology |
Medium |
39714773
|
| 2025 |
PFKM translocates to the macrophage nucleus during sepsis and interacts with p53 (identified by Co-IP/mass spectrometry); nuclear PFKM promotes p53 acetylation at K120, enhancing p53 binding to the Pdcd1 promoter to drive PD-1 transcription, thereby suppressing macrophage phagocytosis via a non-glycolytic moonlighting function. |
Co-IP coupled with mass spectrometry, immunofluorescence for nuclear localization, dual-luciferase reporter, ChIP, transcriptomic sequencing, nanobody blocking, sepsis mouse models |
Theranostics |
High |
41608568
|
| 2025 |
PFKM drives lactate accumulation which promotes global and H3K18 lactylation in atrial fibroblasts; P300-mediated H3K18 lactylation at the TGF-β1 promoter upregulates TGF-β1 transcription, activating cardiac fibroblasts and contributing to atrial fibrosis. AAV-mediated atrial PFKM expression confirmed PFKM as the pivotal glycolytic driver in this pathway. |
AAV-mediated PFKM overexpression in vivo, glycolysis inhibitor (2-DG) treatment, ChIP for H3K18la at TGF-β1 promoter, primary cardiac fibroblast activation assays |
Advanced science |
Medium |
40569576
|
| 2025 |
PFKM promotes gastric cancer progression by interacting with CNTN1 and facilitating enrichment of H3K18 lactylation at the CNTN1 promoter, activating CNTN1 transcription; CNTN1 overexpression reverses the inhibitory effects of PFKM knockdown. |
Co-immunoprecipitation (PFKM-CNTN1 interaction), dual-luciferase reporter, ChIP for H3K18la at CNTN1 promoter, knockdown/overexpression rescue, xenograft |
Applied biochemistry and biotechnology |
Medium |
40608258
|
| 2025 |
FTO demethylase elevates C-Jun mRNA in a m6A-YTHDF2-dependent manner, and C-Jun transcriptionally upregulates PFKM expression, thereby promoting glycolysis in pancreatic ductal adenocarcinoma; FTO inhibitors suppress PDAC growth in organoid and xenograft models. |
m6A-seq, transcriptome sequencing, metabolomics, FTO-conditional knockout mouse model, organoids, xenograft, ChIP for C-Jun at PFKM promoter |
Cell death & disease |
Medium |
41184232
|
| 2022 |
miR-21a-5p in bone marrow MSC-derived exosomes directly represses PFKM expression (a rate-limiting glycolytic enzyme) in tubular epithelial cells, attenuating glycolysis and renal fibrosis; knockdown of miR-21a-5p abolished the renoprotective effect of MSC-Exos. |
miRNA sequencing, in vitro miR-21a-5p targeting validation, UUO mouse model, glycolysis assays |
Cell death & disease |
Medium |
36253358
|
| 2012 |
HSV-1 infection increases PFK-1 expression and triggers phosphorylation of PFK-1 at serine residues, increasing total PFK-1 activity and glycolysis; PFK-1 knockdown impairs HSV-1 replication. |
Western blot, glucose uptake/lactate efflux assays, serine phosphorylation detection, PFK-1 siRNA knockdown, viral replication assay |
Biochimica et biophysica acta |
Medium |
22542512
|
| 2006 |
AMPK phosphorylates and activates PFK-2 post-mortem, increasing fructose-2,6-diphosphate levels which then up-regulate PFK-1 (PFKM) activity; earlier AMPK activation in PSE porcine muscle leads to faster glycolysis and lower pH. |
Biochemical activity assays (AMPK, PFK-1, glycogen phosphorylase, pyruvate kinase), fructose-2,6-diphosphate measurement, pH and metabolite quantification in porcine muscle |
Journal of agricultural and food chemistry |
Medium |
16848549
|
| 1989 |
A Zn2+-binding protein (identified as parathymosin-alpha) reversibly inactivates phosphofructokinase-1 (PFK-1/PFKM) in a Zn2+-dependent manner via its 43-amino-acid zinc-binding domain. |
cDNA sequencing, protein sequence comparison, in vitro PFK-1 inactivation assay with Zn2+-binding protein |
FEBS letters |
Medium |
2759245
|
| 2025 |
PFKM influences exosome release by modulating RAB8B expression; the PFKM-RAB8B interaction promotes chemoresistance in lung adenocarcinoma by impacting apoptosis and glycolytic metabolism, with drug-resistant cells releasing glycolytically active exosomes that transfer chemoresistance to sensitive cells. |
Targeted metabolomics (FBP/F6P ratio as PFKM activity proxy), exosome isolation and characterization, PFKM-RAB8B interaction analysis, knockdown/overexpression |
Journal of pharmaceutical analysis |
Low |
42057963
|
| 2022 |
HDAC1 inhibits H3K27ac-induced transcription of PFKM in doxorubicin-treated cardiomyocytes; PFKM overexpression inhibits DOX-induced apoptosis and maintains glycolysis and oxidative phosphorylation, while PFKM silencing promotes apoptosis. |
RT-PCR, immunoblotting, PFKM overexpression/knockdown, Seahorse metabolic assay, apoptosis assay in H9c2 cells |
Scientific reports |
Low |
35804014
|
| 2024 |
Chloroquine (CQ) directly binds PFKM and inhibits its expression and enzymatic activity, thereby blocking the Warburg effect in colorectal cancer cells; additionally, CHKA downregulation also decreases PFKM expression and activity. |
Target identification and binding verification (method not fully described in abstract), enzymatic activity assay, knockdown/expression analysis |
International journal of biological sciences |
Low |
39990656
|
| 2026 |
PFKM drives glycolytic reprogramming leading to lactate accumulation, which promotes H3K18 lactylation at the Rela promoter via histone modification, activating NF-κB pathway and exacerbating renal inflammation and fibrosis; AAV9-mediated PFKM knockdown alleviated FA-induced renal fibrosis in mice. |
AAV9 PFKM knockdown/overexpression in renal tubular cells, RNA-seq, CUT&Tag for H3K18la, ChIP-qPCR, metabolic analysis, histological staining |
Cellular and molecular life sciences |
Medium |
41711888
|
| 1996 |
Two mutations in the PFKM gene (G1127A transition destroying the 5' donor site of intron 13 causing 155-nt intron retention, and an a-to-g change in intron 16 creating a new acceptor splice site causing 63-nt intron retention) result in compound heterozygous Tarui disease (GSD VII) with predicted premature translation termination. |
Genomic DNA amplification, cDNA sequencing, splicing analysis, restriction mapping |
American journal of human genetics |
Medium |
8659544
|
| 1982 |
The human PFKM locus was assigned to chromosome 1 (region cen to q32) using somatic cell hybrid analysis with anti-human M subunit-specific monoclonal antibody. |
Somatic cell hybrid panel analysis, monoclonal antibody-based isozyme detection, chromosome marker analysis |
Somatic cell genetics |
Medium |
6213050
|
| 1996 |
PFKM maps to chromosome 12q13 (not chromosome 1 as previously reported); PCR with somatic cell hybrid panel showed 100% concordance with chromosome 12, and FISH with CEPH YAC 762G4 localized PFKM centromeric to DAGK at 12q13.3. |
PCR with somatic cell hybrid panel, fluorescence in situ hybridization (FISH), genetic mapping with microsatellite marker |
Genomics |
High |
8661033
|
| 2024 |
In porcine trophoblast cells, miR-92b-3p targets PFKM mRNA (validated by dual-luciferase reporter assay); PFKM knockdown promoted PTr2 cell proliferation and migration, and uterine miR-92b-3p downregulation reduced embryo implantation rates in mice. |
Dual-luciferase reporter assay, RT-qPCR, Western blot, siRNA knockdown of PFKM, mouse uterine miRNA manipulation |
International journal of molecular sciences |
Low |
36555776
|