Abstract

Cancer is a metabolic disease in which abnormally proliferating cancer cells rewire metabolic pathways in the tumor microenvironment (TME). Molecular reprogramming in the TME helps cancer cells to fulfill elevated metabolic demands for bioenergetics and cellular biosynthesis. One of the ways through which cancer cell achieve this is by regulating the expression of metabolic enzymes. Lactate dehydrogenase (LDH) is the primary metabolic enzyme that converts pyruvate to lactate and vice versa. LDH also plays a significant role in regulating nutrient exchange between tumor and stroma. Thus, targeting human lactate dehydrogenase for treating advanced carcinomas may be of benefit. LDHA and LDHB, two isoenzymes of LDH, participate in tumor stroma metabolic interaction and exchange of metabolic fuel and thus could serve as potential anticancer drug targets. This article reviews recent research discussing the roles of lactate dehydrogenase in cancer metabolism. As molecular regulation of LDHA and LDHB in different cancer remains obscure, we also review signaling pathways regulating LDHA and LDHB expression. We highlight on the role of small molecule inhibitors in targeting LDH activity and we emphasize the development of safer and more effective LDH inhibitors. We trust that this review will also generate interest in designing combination therapies based on LDH inhibition, with LDHA being targeted in tumors and LDHB in stromal cells for better treatment outcome.

Highlights

  • The tumor microenvironment (TME) is a complex dynamic cellular environment comprised of tumor cells, stromal cells, blood vessels, extracellular matrix (ECM), growth factors and cellular metabolites [1]

  • We trust that this review will generate interest in designing combination therapies based on Lactate dehydrogenase (LDH) inhibition, with LDHA being targeted in tumors and Lactate dehydrogenase B (LDHB) in stromal cells for better treatment outcome

  • We summarize the molecular regulation of LDHA and LDHB and emphasize on the importance of lactate; a metabolic substrate of LDH as an additional metabolic energy source and its diverse role in the TME

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Summary

Introduction

The tumor microenvironment (TME) is a complex dynamic cellular environment comprised of tumor cells, stromal cells, blood vessels, extracellular matrix (ECM), growth factors and cellular metabolites [1]. The “Warburg” lactate produced and extruded into the microenvironment acts as an alternative metabolic substrate for oxygenated tumor cells in the TME. This adaption of preferential utilization of lactate by oxygenated tumor cells benefits the neighboring hypoxic tumor cells that can utilize the spared glucose [6]. Lactate dehydrogenase (LDH) is one of the key metabolic enzymes present in the TME that play essential role in conversion of pyruvate to lactate and vice versa making it an important player in cancer metabolism [7]. We summarize the molecular regulation of LDHA and LDHB and emphasize on the importance of lactate; a metabolic substrate of LDH as an additional metabolic energy source and its diverse role in the TME. This review highlights the advantage of using complimentary therapies based upon targeting metabolic enzymes in the TME for better outcomes

Lactate Dehydrogenase
LDHA in Cancers
HIF-1 and LDHA
FOXM1 and LDHA
KLF4 and LDHA
Other Pathways
LDHB in Cancers
LDHB Promoter Hypermethylation
LDHB Regulation by Different Pathways
LDH-Mediated Metabolic Exchange between Cancer Cells and Stromal CAFs
Lactate: A Substrate for LDH
Role of Lactate in Regulating Immunometabolism in the TME
Serum LDH Profile in Cancers and Clinical Relevance
Future Directions in Therapeutic Designing
Small Molecule Inhibitors
Molecular Inhibition of LDHA and LDHB
Blocking Lactate Exchange between Tumor and Stroma
Findings
10. Conclusions
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