The dichotomous role of the glycolytic metabolism pathway in cancer metastasis: Interplay with the complex tumor microenvironment and novel therapeutic strategies.
Antineoplastic Agents
/ pharmacology
Ascorbic Acid
/ metabolism
Energy Metabolism
Glucose
/ metabolism
Glycolysis
Humans
L-Lactate Dehydrogenase
/ antagonists & inhibitors
Metabolic Networks and Pathways
/ drug effects
Mitochondria
/ metabolism
Molecular Targeted Therapy
Neoplasms
/ drug therapy
Oxidative Phosphorylation
/ drug effects
Oxidative Stress
/ drug effects
Reactive Oxygen Species
/ metabolism
Signal Transduction
Stromal Cells
/ metabolism
Tumor Microenvironment
Glycolysis
LDH
Metastasis
Tumor microenvironment
Vitamin C
Journal
Seminars in cancer biology
ISSN: 1096-3650
Titre abrégé: Semin Cancer Biol
Pays: England
ID NLM: 9010218
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
24
06
2019
revised:
17
08
2019
accepted:
20
08
2019
pubmed:
25
8
2019
medline:
18
12
2020
entrez:
25
8
2019
Statut:
ppublish
Résumé
Cancer metastasis to distant organs is initiated by tumor cells that disseminate from primary heterogeneous tumors. The subsequent growth and survival of tumor metastases depend on different metabolic changes, which constitute one of the enigmatic properties of tumor cells. Aerobic glycolysis, 'the Warburg effect', contributes to tumor energy supply, by oxidizing glucose in a faster manner compared to oxidative phosphorylation, leading to an increased lactate production by lactate dehydrogenase A (LDH-A), which in turn affects the immune response. Surrounding stromal cells contribute to feedback mechanisms further prompting the acquisition of pro-invasive metabolic features. Hence, therapeutic strategies targeting the glycolytic pathway are intensively investigated, with a special interest on their anti-metastatic properties. Various small molecules, such as LDH-A inhibitors, have shown pre-clinical activity against different cancer types, and blocking LDH-A could also help in designing future complimentary therapies. Modulation of specific targets in cells with an altered glycolytic metabolism should indeed result in a milder and distinct toxicity profile, compared to conventional cytotoxic therapy, while a combination treatment with vitamin C leading to increasing reactive oxygen species levels, should further inhibit cancer cell survival and invasion. In this review we describe the impact of metabolic reprogramming in cancer metastasis, the contribution of lactate in this aberrant process and its effect on oncogenic processes. Furthermore, we discuss experimental compounds that target glycolytic metabolism, such as LDH-A inhibitors, and their potential to improve current and experimental therapeutics against metastatic tumors.
Identifiants
pubmed: 31445217
pii: S1044-579X(19)30180-4
doi: 10.1016/j.semcancer.2019.08.025
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Reactive Oxygen Species
0
L-Lactate Dehydrogenase
EC 1.1.1.27
Glucose
IY9XDZ35W2
Ascorbic Acid
PQ6CK8PD0R
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
238-248Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that there are no conflicts of interest.