Flavonoids against the Warburg phenotype-concepts of predictive, preventive and personalised medicine to cut the Gordian knot of cancer cell metabolism.

Aerobic glycolysis Age Aggressive metastatic disease Anticancer effect Biomarker patterns Cancer Carcinogenesis Cell metabolism Chemoresistance Co-morbidities Disease manifestation FDG-PET Flavonoids Glucose intake Glucose metabolism Glycolysis Glycolytic inhibitors HIF-1 Individual outcome Individualised patient profiles Ischemic lesions Liquid biopsy Liver malignancy Magnetic resonance spectroscopy Malignancy Metabolic reprogramming Microcirculation Modifiable risk factors Multi-omics Oxidative phosphorylation PET-CT Palliative medicine Patient stratification Pleiotropic activity Polyphenols Positron emission tomography Predictive preventive personalised medicine (PPPM / 3PM) Pregnancy Prognosis Prognostic markers Proliferation Prostate cancer Radioresistance Risk assessment Systemic hypoxia Treatment algorithms Triple-negative breast cancer Tumour imaging Warburg phenotype

Journal

The EPMA journal
ISSN: 1878-5077
Titre abrégé: EPMA J
Pays: Switzerland
ID NLM: 101517307

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 16 06 2020
accepted: 30 06 2020
entrez: 27 8 2020
pubmed: 28 8 2020
medline: 28 8 2020
Statut: epublish

Résumé

The Warburg effect is characterised by increased glucose uptake and lactate secretion in cancer cells resulting from metabolic transformation in tumour tissue. The corresponding molecular pathways switch from oxidative phosphorylation to aerobic glycolysis, due to changes in glucose degradation mechanisms known as the 'Warburg reprogramming' of cancer cells. Key glycolytic enzymes, glucose transporters and transcription factors involved in the Warburg transformation are frequently dysregulated during carcinogenesis considered as promising diagnostic and prognostic markers as well as treatment targets. Flavonoids are molecules with pleiotropic activities. The metabolism-regulating anticancer effects of flavonoids are broadly demonstrated in preclinical studies. Flavonoids modulate key pathways involved in the Warburg phenotype including but not limited to PKM2, HK2, GLUT1 and HIF-1. The corresponding molecular mechanisms and clinical relevance of 'anti-Warburg' effects of flavonoids are discussed in this review article. The most prominent examples are provided for the potential application of targeted 'anti-Warburg' measures in cancer management. Individualised profiling and patient stratification are presented as powerful tools for implementing targeted 'anti-Warburg' measures in the context of predictive, preventive and personalised medicine.

Identifiants

pubmed: 32843908
doi: 10.1007/s13167-020-00217-y
pii: 217
pmc: PMC7429635
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

377-398

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Marek Samec (M)

Clinic of Obstetrics and Gynecology, Jessenius Faculty of Medicine, Comenius University in Bratislava, 03601 Martin, Slovakia.

Alena Liskova (A)

Clinic of Obstetrics and Gynecology, Jessenius Faculty of Medicine, Comenius University in Bratislava, 03601 Martin, Slovakia.

Lenka Koklesova (L)

Clinic of Obstetrics and Gynecology, Jessenius Faculty of Medicine, Comenius University in Bratislava, 03601 Martin, Slovakia.

Samson Mathews Samuel (SM)

Department of Physiology and Biophysics, Weill Cornell Medicine in Qatar, Education City, Qatar Foundation, 24144, Doha, Qatar.

Kevin Zhai (K)

Department of Physiology and Biophysics, Weill Cornell Medicine in Qatar, Education City, Qatar Foundation, 24144, Doha, Qatar.

Constanze Buhrmann (C)

Musculoskeletal Research Group and Tumour Biology, Chair of Vegetative Anatomy, Institute of Anatomy, Faculty of Medicine, Ludwig-Maximilian-University Munich, 80336 Munich, Germany.

Elizabeth Varghese (E)

Department of Physiology and Biophysics, Weill Cornell Medicine in Qatar, Education City, Qatar Foundation, 24144, Doha, Qatar.

Mariam Abotaleb (M)

Department of Physiology and Biophysics, Weill Cornell Medicine in Qatar, Education City, Qatar Foundation, 24144, Doha, Qatar.

Tawar Qaradakhi (T)

Institute for Health and Sport, Victoria University, Melbourne, VIC 3011 Australia.

Anthony Zulli (A)

Institute for Health and Sport, Victoria University, Melbourne, VIC 3011 Australia.

Martin Kello (M)

Department of Pharmacology, Faculty of Medicine, P. J. Šafarik University, 040 11 Košice, Slovakia.

Jan Mojzis (J)

Department of Pharmacology, Faculty of Medicine, P. J. Šafarik University, 040 11 Košice, Slovakia.

Pavol Zubor (P)

Department of Gynecologic Oncology, Norwegian Radium Hospital, Oslo University Hospital, 0379 Oslo, Norway.
OBGY Health & Care, Ltd., 01001 Zilina, Slovak Republic.

Taeg Kyu Kwon (TK)

Department of Immunology and School of Medicine, Keimyung University, Dalseo-Gu, Daegu, 426 01 South Korea.

Mehdi Shakibaei (M)

Musculoskeletal Research Group and Tumour Biology, Chair of Vegetative Anatomy, Institute of Anatomy, Faculty of Medicine, Ludwig-Maximilian-University Munich, 80336 Munich, Germany.

Dietrich Büsselberg (D)

Department of Physiology and Biophysics, Weill Cornell Medicine in Qatar, Education City, Qatar Foundation, 24144, Doha, Qatar.

Gustavo R Sarria (GR)

Department of Radiation Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.

Olga Golubnitschaja (O)

Predictive, Preventive Personalised (3P) Medicine, Department of Radiation Oncology, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.

Peter Kubatka (P)

Department of Medical Biology, Jessenius Faculty of Medicine, Comenius University in Bratislava, 036 01 Martin, Slovakia.

Classifications MeSH