The oncogenic and clinical implications of lactate induced immunosuppression in the tumour microenvironment. (1st March 2021)

• Record Type: Journal Article
• Authors: Hayes, Conall; Donohoe, Claire L.; Davern, Maria; Donlon, Noel E.
• Is Part Of: Cancer letters. Volume 500(2021)
• Page Start: 75
• Page End: 86
• Publication Date: 2021-03-01
• Subjects: Warburg effect -- Metabolic reprogramming -- Immune evasion -- Oncometabolite -- Predictive and prognostic biomarker; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Electronic journals; 616.994
• DOI: 10.1016/j.canlet.2020.12.021
• Languages: English
• ISSNs: 0304-3835

Abstract

Abstract: The tumour microenvironment is of critical importance in cancer development and progression and includes the surrounding stromal and immune cells, extracellular matrix, and the milieu of metabolites and signalling molecules in the intercellular space. To support sustained mitotic activity cancer cells must reconfigure their metabolic phenotype. Lactate is the major by-product of such metabolic alterations and consequently, accumulates in the tumour. Lactate actively contributes to immune evasion, a hallmark of cancer, by directly inhibiting immune cell cytotoxicity and proliferation. Furthermore, lactate can recruit and induce immunosuppressive cell types, such as regulatory T cells, tumour-associated macrophages, and myeloid-derived suppressor cells which further suppress anti-tumour immune responses. Given its roles in oncogenesis, measuring intratumoural and systemic lactate levels has shown promise as a both predictive and prognostic biomarker in several cancer types. The efficacies of many anti-cancer therapies are limited by an immunosuppressive TME in which lactate is a major contributor, therefore, targeting lactate metabolism is a priority. Developing inhibitors of key proteins in lactate metabolism such as GLUT1, hexokinase, LDH, MCT and HIF have shown promise in preclinical studies, however there is a corresponding lack of success in human trials so far. This may be explained by a weakness of preclinical models that fail to reproduce the complexities of metabolic interactions in natura . The future of these therapies may be as an adjunct to more conventional treatments. Highlights: Lactate accumulates in tumours due to metabolic derangements in cancer cells. Lactate can suppress immune cell function directly as well as indirectly by recruiting immunosuppressive cell types. Lactate has potential as a prognostic and predictive biomarker. Despite positive preclinical results, targeting lactate metabolism has not yet led to clinically successful therapies.