» Articles » PMID: 37253634

Glycolytic Regulatory Enzyme PFKFB3 As a Prognostic and Tumor Microenvironment Biomarker in Human Cancers

Overview
Specialty Geriatrics
Date 2023 May 30
PMID 37253634
Authors
Affiliations
Soon will be listed here.
Abstract

The 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFK-2/FBPase-2, PFKFB3) is a glycolysis regulatory enzyme and plays a key role in oncogenesis of several cancers. However, the systematic study of crosstalk between PFKFB3 and Tumor microenvironment (TME) in pan-cancer has less been examined. In this study, we conducted a comprehensive analysis of the relationship between expression, patient prognostic, Tumor mutational burden (TMB), Microsatellite instability (MSI), DNA mismatch repair (MMR), and especially TME, including immune infiltration, immune regulator, and immune checkpoint, across 33 types of tumors using datasets of The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO). We found that expression was significantly correlated with patient prognostic and TME factors in various tumors. Moreover, we confirmed that PFKFB3 was an independent prognostic factor for kidney renal papillary cell carcinoma (KIRP), and established a risk prognostic model based on the expression of as a clinical risk factor, which has a good predictive ability. Our study indicated that PFKFB3 is a potent regulatory factor for TME and has the potential to be a valuable prognostic biomarker in human tumor therapy.

Citing Articles

PFKFB3 Connects Glycolytic Metabolism with Endothelial Dysfunction in Human and Rodent Obesity.

Batori R, Bordan Z, Padgett C, Huo Y, Chen F, Atawia R Antioxidants (Basel). 2025; 14(2).

PMID: 40002359 PMC: 11851787. DOI: 10.3390/antiox14020172.


Impact of glycolysis enzymes and metabolites in regulating DNA damage repair in tumorigenesis and therapy.

Sun F, Li W, Du R, Liu M, Cheng Y, Ma J Cell Commun Signal. 2025; 23(1):44.

PMID: 39849559 PMC: 11760674. DOI: 10.1186/s12964-025-02047-9.


Analyzing the impact of metabolism on immune cells in tumor microenvironment to promote the development of immunotherapy.

Long Y, Shi H, He Y, Qi X Front Immunol. 2024; 14:1307228.

PMID: 38264667 PMC: 10804850. DOI: 10.3389/fimmu.2023.1307228.


Hitting the Sweet Spot: How Glucose Metabolism Is Orchestrated in Space and Time by Phosphofructokinase-1.

Campos M, Albrecht L Cancers (Basel). 2024; 16(1).

PMID: 38201444 PMC: 10778546. DOI: 10.3390/cancers16010016.


Human Triosephosphate Isomerase Is a Potential Target in Cancer Due to Commonly Occurring Post-Translational Modifications.

Enriquez-Flores S, de la Mora-de la Mora I, Garcia-Torres I, Flores-Lopez L, Martinez-Perez Y, Lopez-Velazquez G Molecules. 2023; 28(16).

PMID: 37630415 PMC: 10459230. DOI: 10.3390/molecules28166163.

References
1.
Fumet J, Truntzer C, Yarchoan M, Ghiringhelli F . Tumour mutational burden as a biomarker for immunotherapy: Current data and emerging concepts. Eur J Cancer. 2020; 131:40-50. PMC: 9473693. DOI: 10.1016/j.ejca.2020.02.038. View

2.
Cui X, Zhang X, Liu M, Zhao C, Zhang N, Ren Y . A pan-cancer analysis of the oncogenic role of staphylococcal nuclease domain-containing protein 1 (SND1) in human tumors. Genomics. 2020; 112(6):3958-3967. DOI: 10.1016/j.ygeno.2020.06.044. View

3.
Wang C, Qu J, Yan S, Gao Q, Hao S, Zhou D . PFK15, a PFKFB3 antagonist, inhibits autophagy and proliferation in rhabdomyosarcoma cells. Int J Mol Med. 2018; 42(1):359-367. PMC: 5979828. DOI: 10.3892/ijmm.2018.3599. View

4.
Chen D, Ning W, Jiang Z, Peng Z, Zhu L, Zhuang S . Glycolytic activation of peritumoral monocytes fosters immune privilege via the PFKFB3-PD-L1 axis in human hepatocellular carcinoma. J Hepatol. 2019; 71(2):333-343. DOI: 10.1016/j.jhep.2019.04.007. View

5.
Vander Heiden M, Cantley L, Thompson C . Understanding the Warburg effect: the metabolic requirements of cell proliferation. Science. 2009; 324(5930):1029-33. PMC: 2849637. DOI: 10.1126/science.1160809. View