Lactate: a metabolic key player in cancer.

Increased glucose uptake and accumulation of lactate, even under normoxic conditions (i.e., aerobic glycolysis or the Warburg Effect), is a common feature of cancer cells. This phenomenon clearly indicates that lactate is not a surrogate of tumor hypoxia. Tumor lactate can predict for metastases and overall survival of patients, as shown by several studies of different entities. Metastasis of tumors is promoted by lactate-induced secretion of hyaluronan by tumor-associated fibroblasts that create a milieu favorable for migration. Lactate itself has been found to induce the migration of cells and cell clusters. Furthermore, radioresistance has been positively correlated with lactate concentrations, suggesting an antioxidative capacity of lactate. Findings on interactions of tumor metabolites with immune cells indicate a contribution of lactate to the immune escape. Furthermore, lactate bridges the gap between high lactate levels in wound healing, chronic inflammation, and cancer development. Tumor cells ensure sufficient oxygen and nutrient supply for proliferation through lactate-induced secretion of VEGF, resulting in the formation of new vessels. In summary, accumulation of lactate in solid tumors is a pivotal and early event in the development of malignancies. The determination of lactate should enter further clinical trials to confirm its relevance in cancer biology.

[1]  Hanna Y. Irie,et al.  Antioxidant and oncogene rescue of metabolic defects caused by loss of matrix attachment , 2009, Nature.

[2]  C. Groussard,et al.  Free radical scavenging and antioxidant effects of lactate ion: an in vitro study. , 2000, Journal of applied physiology.

[3]  W. Mueller‐Klieser,et al.  The anti-oxidant capacity of tumour glycolysis , 2009, International journal of radiation biology.

[4]  R. Stern Hyaluronidases in cancer biology. , 2008, Seminars in cancer biology.

[5]  W. Weber,et al.  Tumor Cell Metabolism Imaging , 2008, Journal of Nuclear Medicine.

[6]  H. Shime,et al.  IL-23-dependent and -independent enhancement pathways of IL-17A production by lactic acid. , 2011, International immunology.

[7]  Matthias Schäfer,et al.  Cancer as an overhealing wound: an old hypothesis revisited , 2008, Nature Reviews Molecular Cell Biology.

[8]  R. Deberardinis Is cancer a disease of abnormal cellular metabolism? New angles on an old idea , 2008, Genetics in Medicine.

[9]  H. Christofk,et al.  Rapidly Proliferating Cells Evidence for an Alternative Glycolytic Pathway in , 2010 .

[10]  Stefan Walenta,et al.  Lactate: mirror and motor of tumor malignancy. , 2004, Seminars in radiation oncology.

[11]  W. Mueller‐Klieser,et al.  Manipulation of glycolysis in malignant tumors: fantasy or therapy? , 2010, Current medicinal chemistry.

[12]  Gregor Rothe,et al.  Inhibitory effect of tumor cell-derived lactic acid on human T cells. , 2007, Blood.

[13]  M. Baumann,et al.  Co-localisation of hypoxia and perfusion markers with parameters of glucose metabolism in human squamous cell carcinoma (hSCC) xenografts , 2009, International journal of radiation biology.

[14]  A. Mackensen,et al.  Tumor-derived lactic acid modulates dendritic cell activation and antigen expression. , 2006, Blood.

[15]  Pierre Sonveaux,et al.  Lactate influx through the endothelial cell monocarboxylate transporter MCT1 supports an NF-κB/IL-8 pathway that drives tumor angiogenesis. , 2011, Cancer research.

[16]  K. Greulich,et al.  Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes. , 2004, Genomics.

[17]  T. K. Hunt,et al.  Lactate stimulates endothelial cell migration , 2006, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[18]  P. Oefner,et al.  Lactic Acid and Acidification Inhibit TNF Secretion and Glycolysis of Human Monocytes , 2009, The Journal of Immunology.

[19]  T. K. Hunt,et al.  Lactate, with oxygen, incites angiogenesis. , 2008, Advances in experimental medicine and biology.

[20]  Stefan Walenta,et al.  Lactate enhances motility of tumor cells and inhibits monocyte migration and cytokine release. , 2011, International journal of oncology.

[21]  T. Reichert,et al.  Metabolic and proteomic differentials in head and neck squamous cell carcinomas and normal gingival tissue , 2011, Journal of Cancer Research and Clinical Oncology.

[22]  Huasheng Lu,et al.  Hypoxia-inducible Factor 1 Activation by Aerobic Glycolysis Implicates the Warburg Effect in Carcinogenesis* , 2002, The Journal of Biological Chemistry.

[23]  Saroj P. Mathupala,et al.  The pivotal roles of mitochondria in cancer: Warburg and beyond and encouraging prospects for effective therapies. , 2010, Biochimica et biophysica acta.

[24]  O. Warburg On the origin of cancer cells. , 1956, Science.

[25]  J. Rathmell,et al.  Cutting Edge: Distinct Glycolytic and Lipid Oxidative Metabolic Programs Are Essential for Effector and Regulatory CD4+ T Cell Subsets , 2011, The Journal of Immunology.

[26]  P. Oefner,et al.  Lactate promotes glioma migration by TGF-beta2-dependent regulation of matrix metalloproteinase-2. , 2009, Neuro-oncology.

[27]  C. Ong,et al.  Metabolic profiling in colorectal cancer reveals signature metabolic shifts during tumorigenesis. , 2010, Molecular & cellular proteomics : MCP.

[28]  Susan M. Chang,et al.  Evaluation of MR markers that predict survival in patients with newly diagnosed GBM prior to adjuvant therapy , 2008, Journal of Neuro-Oncology.

[29]  Michael Baumann,et al.  Glycolytic metabolism and tumour response to fractionated irradiation. , 2010, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[30]  A. Mackensen,et al.  Suppression of T-cell responses by tumor metabolites , 2011, Cancer Immunology, Immunotherapy.

[31]  A. Levine,et al.  The Control of the Metabolic Switch in Cancers by Oncogenes and Tumor Suppressor Genes , 2010, Science.

[32]  Ilwoo Park,et al.  Hyperpolarized 13C magnetic resonance metabolic imaging: application to brain tumors. , 2010, Neuro-oncology.

[33]  E. Rofstad,et al.  High lactate levels predict likelihood of metastases, tumor recurrence, and restricted patient survival in human cervical cancers. , 2000, Cancer research.

[34]  S. Kornbluth,et al.  The engine driving the ship: metabolic steering of cell proliferation and death , 2010, Nature Reviews Molecular Cell Biology.

[35]  E. Gottlieb,et al.  Targeting metabolic transformation for cancer therapy , 2010, Nature Reviews Cancer.