The effect of extracellular vesicles derived from oral squamous cell carcinoma on the metabolic profile of oral fibroblasts

被引:0
作者
Lipka, Aleksandra [1 ]
Soland, Tine M. [1 ]
Nieminen, Anni I. [2 ]
Sapkota, Dipak [1 ]
Haug, Trude M. [1 ]
Galtung, Hilde K. [1 ]
机构
[1] Univ Oslo, Inst Oral Biol, Fac Dent, Oslo, Norway
[2] Univ Helsinki, Inst Mol Med Finland, Helsinki, Finland
关键词
oral cancer; oral squamous cell carcinoma; fibroblasts; phenotype; metabolic profile; extracellular vesicles; EV; OSCC; CANCER-ASSOCIATED FIBROBLASTS; ACID; EPIDEMIOLOGY; MACROPHAGES;
D O I
10.3389/fmolb.2025.1492282
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction Oral cancer is one of the most common forms of head and neck cancers. Oral squamous cell carcinoma (OSCC) accounts for more than 90% of the oral malignancies. The molecular pathogenesis of OSCC is complex as it involves altered expression of specific genes and proteins, but also comprises changes in metabolic processes. It is suggested that extracellular vesicles (EVs) released by cancer cells may contribute to cancer development and metastasis by recruiting and changing phenotype of normal cells that surround the tumor.Methods The aim of the project was to characterize the effect of OSCC EVs on the metabolic profile of normal oral fibroblasts (NOFs). Targeted liquid chromatography mass spectrometry metabolic profiling was performed on control cells and NOFs exposed to OSCC EVs for 24 and 48 h.Results Analysis of detected metabolites revealed that OSCC EVs affected NOFs the most after 24 h of exposure. Among metabolites that were significantly altered at 24 h, pyruvate, ATP, UTP, coenzyme A, and dihydroxyacetone phosphate were upregulated, while fatty acids such as nervonic acid, linoleate, oleate, palmitoleic acid, and docosahexaenoic acid were downregulated. These findings were supported by Western blotting of pyruvate kinase M2 (PKM2) and aldolase, fructose-bisphosphate A (ALDOA).Conclusion The metabolic pathways of glycolysis, citric acid cycle, and amino acid metabolism were enriched, suggesting that OSCC EVs cause phenotype switch in NOFs that may contribute to acquiring a pro-tumorigenic phenotype.
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页数:12
相关论文
共 56 条
[1]   The World of Oral Cancer and Its Risk Factors Viewed from the Aspect of MicroRNA Expression Patterns [J].
Aghiorghiesei, Ovidiu ;
Zanoaga, Oana ;
Nutu, Andreea ;
Braicu, Cornelia ;
Campian, Radu Septimiu ;
Lucaciu, Ondine ;
Neagoe, Ioana Berindan .
GENES, 2022, 13 (04)
[2]   Significance of Cancer-Associated Fibroblasts in the Interactions of Cancer Cells with the Tumor Microenvironment of Heterogeneous Tumor Tissue [J].
Arima, Yoshimi ;
Matsueda, Satoko ;
Saya, Hideyuki .
CANCERS, 2023, 15 (09)
[3]  
Auber M, 2022, J EXTRACELL BIOL, V1, DOI 10.1002/jex2.46
[4]   Oral Squamous Cell Carcinoma and Concomitant Primary Tumors, What Do We Know? A Review of the Literature [J].
Badwelan, Mohammed ;
Muaddi, Hasan ;
Ahmed, Abeer ;
Lee, Kyungjun T. ;
Tran, Simon D. .
CURRENT ONCOLOGY, 2023, 30 (04) :3721-3734
[5]   Roles of Mitochondria in Oral Squamous Cell Carcinoma Therapy: Friend or Foe? [J].
Bai, Junqiang ;
Wu, Luping ;
Wang, Xinmiao ;
Wang, Yifan ;
Shang, Zhengjun ;
Jiang, Erhui ;
Shao, Zhe .
CANCERS, 2022, 14 (23)
[6]   Extracellular Vesicles in Cancer: Cell-to-Cell Mediators of Metastasis [J].
Becker, Annette ;
Thakur, Basant Kumar ;
Weiss, Joshua Mitchell ;
Kim, Han Sang ;
Peinado, Hector ;
Lyden, David .
CANCER CELL, 2016, 30 (06) :836-848
[7]   Metabolomics enables precision medicine: "A White Paper, Community Perspective" [J].
Beger, Richard D. ;
Dunn, Warwick ;
Schmidt, Michael A. ;
Gross, Steven S. ;
Kirwan, Jennifer A. ;
Cascante, Marta ;
Brennan, Lorraine ;
Wishart, David S. ;
Oresic, Matej ;
Hankemeier, Thomas ;
Broadhurst, David I. ;
Lane, Andrew N. ;
Suhre, Karsten ;
Kastenmueller, Gabi ;
Sumner, Susan J. ;
Thiele, Ines ;
Fiehn, Oliver ;
Kaddurah-Daouk, Rima .
METABOLOMICS, 2016, 12 (09)
[8]  
Bewley AF, 2017, CLIN DERMATOL, V35, P461, DOI [10.1016/j.clindermatol.2017.06.008, 10.1016/j.clindermato1.2017.06.008]
[9]   The Acidic Tumor Microenvironment as a Driver of Cancer [J].
Boedtkjer, Ebbe ;
Pedersen, Stine F. .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 82, 2020, 82 :103-126
[10]  
Borish Larry C., 2003, Journal of Allergy and Clinical Immunology, V111, pS460