Early Neutrophilia Marked by Aerobic Glycolysis Sustains Host Metabolism and Delays Cancer Cachexia

An elevated neutrophil-to-lymphocyte ratio negatively predicts the outcome of patients with cancer and is associated with cachexia, the terminal wasting syndrome. Here, we show using murine model systems of colorectal and pancreatic cancer that neutrophilia in the circulation and multiple organs, accompanied by extramedullary hematopoiesis, is an early event during cancer progression. Transcriptomic and metabolic assessment reveals that neutrophils in tumor-bearing animals utilize aerobic glycolysis, alike to cancer cells. Although pharmacological inhibition of aerobic glycolysis slows down tumor growth in C26 tumor-bearing mice, it precipitates cachexia, thereby shortening overall survival. This negative effect may be explained by our observation that acute depletion of neutrophils in pre-cachectic mice impairs systemic glucose homeostasis secondary to altered hepatic lipid processing. Thus, changes in neutrophil number, distribution and metabolism play an adaptive role in host metabolic homeostasis during cancer progression. Our findings provide insight into early events during cancer progression to cachexia, with implications for therapy.

[1]  J. Norman,et al.  Maturation, developmental site, and pathology dictate murine neutrophil function , 2021, bioRxiv.

[2]  James O. Jones,et al.  Stromal-driven and Amyloid β-dependent induction of neutrophil extracellular traps modulates tumor growth , 2021, Nature Communications.

[3]  M. Pittet,et al.  Durable and controlled depletion of neutrophils in mice , 2020, Nature Communications.

[4]  S. McWeeney,et al.  Circulating myeloid cells invade the central nervous system to mediate cachexia during pancreatic cancer , 2020, eLife.

[5]  L. Nadauld,et al.  An elevated neutrophil-to-lymphocyte ratio associates with weight loss and cachexia in cancer , 2020, Scientific Reports.

[6]  Sven Nahnsen,et al.  The nf-core framework for community-curated bioinformatics pipelines , 2020, Nature Biotechnology.

[7]  S. Ghosh,et al.  Intestinal Barrier Dysfunction, LPS Translocation, and Disease Development , 2020, Journal of the Endocrine Society.

[8]  P. Carmeliet,et al.  PHD1 controls muscle mTORC1 in a hydroxylation-independent manner by stabilizing leucyl tRNA synthetase , 2020, Nature Communications.

[9]  S. Sansom,et al.  GM-CSF drives dysregulated hematopoietic stem cell activity and pathogenic extramedullary myelopoiesis in experimental spondyloarthritis , 2020, Nature Communications.

[10]  B. Haibe-Kains,et al.  GLUT1 inhibition blocks growth of RB1-positive triple negative breast cancer , 2019, Nature Communications.

[11]  Tuo-Hung Hou,et al.  SLIM: Simultaneous Logic-in-Memory Computing Exploiting Bilayer Analog OxRAM Devices , 2018, Scientific Reports.

[12]  K. Egan,et al.  Exploring the prognostic value of the neutrophil-to-lymphocyte ratio in cancer , 2019, Scientific Reports.

[13]  Svenn-Arne Dragly,et al.  Perineuronal nets stabilize the grid cell network , 2019, bioRxiv.

[14]  Xi Xu,et al.  The progress and development of GLUT1 inhibitors targeting cancer energy metabolism. , 2019, Future medicinal chemistry.

[15]  A. Vergnenègre,et al.  Neutrophil-to-lymphocyte ratio evolution is an independent predictor of early progression of second-line nivolumab-treated patients with advanced non-small-cell lung cancers , 2019, PloS one.

[16]  Axel Meyer,et al.  Asymmetric paralog evolution between the “cryptic” gene Bmp16 and its well-studied sister genes Bmp2 and Bmp4 , 2019, Scientific Reports.

[17]  David L. Smith,et al.  Biased efficacy estimates in phase-III dengue vaccine trials due to heterogeneous exposure and differential detectability of primary infections across trial arms , 2019, PloS one.

[18]  G. Bommer,et al.  Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency , 2019, Proceedings of the National Academy of Sciences.

[19]  Xianzhong Xiao,et al.  Inhibition of Aerobic Glycolysis Promotes Neutrophil to Influx to The Infectious Site via CXCR2 In Sepsis. , 2019, Shock.

[20]  M. Pittet,et al.  Efficient and specific Ly6G+ cell depletion: A change in the current practices toward more relevant functional analyses of neutrophils , 2018, bioRxiv.

[21]  S. Anand,et al.  Integrin CD11b activation drives anti-tumor innate immunity , 2018, Nature Communications.

[22]  Nimit L. Patel,et al.  Tumour-elicited neutrophils engage mitochondrial metabolism to circumvent nutrient limitations and maintain immune suppression , 2018, Nature Communications.

[23]  J. Rathmell,et al.  Efferocytosis induces a novel SLC program to promote glucose uptake and lactate release , 2018, Nature.

[24]  G. Shulman,et al.  Mechanisms of Insulin Action and Insulin Resistance. , 2018, Physiological reviews.

[25]  Wenjie Zhu,et al.  Spleen mediates a distinct hematopoietic progenitor response supporting tumor-promoting myelopoiesis , 2018, The Journal of clinical investigation.

[26]  T. Janowitz Cancer: The Tumor-Driven Disease of the Host. , 2018, Cell metabolism.

[27]  Zhigui Li,et al.  The dynamic change of neutrophil to lymphocyte ratio can predict clinical outcome in stage I-III colon cancer , 2018, Scientific Reports.

[28]  Peter A. Calabresi,et al.  Dimethyl fumarate targets GAPDH and aerobic glycolysis to modulate immunity , 2018, Science.

[29]  Patrice D Cani,et al.  Increased gut permeability in cancer cachexia: mechanisms and clinical relevance , 2018, Oncotarget.

[30]  D. Hasselquist,et al.  No evidence that carotenoid pigments boost either immune or antioxidant defenses in a songbird , 2018, Nature Communications.

[31]  Neel S Madhukar,et al.  A Predictive Model for Selective Targeting of the Warburg Effect through GAPDH Inhibition with a Natural Product. , 2017, Cell metabolism.

[32]  S. Jacobsen,et al.  Autophagy-Dependent Generation of Free Fatty Acids Is Critical for Normal Neutrophil Differentiation , 2017, Immunity.

[33]  A. Redfors,et al.  From black and white to shades of grey , 2017 .

[34]  P. Carmeliet,et al.  Prolyl hydroxylase 2 inactivation enhances glycogen storage and promotes excessive neutrophilic responses , 2017, The Journal of clinical investigation.

[35]  M. Kamdar,et al.  Effects of Early Integrated Palliative Care in Patients With Lung and GI Cancer: A Randomized Clinical Trial. , 2017, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[36]  Bo Jiang,et al.  Aerobic glycolysis and high level of lactate in cancer metabolism and microenvironment , 2017, Genes & diseases.

[37]  D. Fearon,et al.  Tumor-Induced IL-6 Reprograms Host Metabolism to Suppress Anti-tumor Immunity , 2016, Cell metabolism.

[38]  P. Mermelstein,et al.  Opposite Effects of mGluR1a and mGluR5 Activation on Nucleus Accumbens Medium Spiny Neuron Dendritic Spine Density , 2016, PloS one.

[39]  N. Xia,et al.  The Clinical Significance of Glycoprotein Phospholipase D Levels in Distinguishing Early Stage Latent Autoimmune Diabetes in Adults and Type 2 Diabetes , 2016, PloS one.

[40]  E. Wagner,et al.  Mechanisms of metabolic dysfunction in cancer-associated cachexia , 2016, Genes & development.

[41]  Eugenia G. Giannopoulou,et al.  Vitamin C selectively kills KRAS and BRAF mutant colorectal cancer cells by targeting GAPDH , 2015, Science.

[42]  D. Kuhns,et al.  Isolation and Functional Analysis of Human Neutrophils , 2015, Current protocols in immunology.

[43]  V. Prasad,et al.  The Strength of Association Between Surrogate End Points and Survival in Oncology: A Systematic Review of Trial-Level Meta-analyses. , 2015, JAMA internal medicine.

[44]  E. Wagner,et al.  A switch from white to brown fat increases energy expenditure in cancer-associated cachexia. , 2014, Cell metabolism.

[45]  Jason W Locasale,et al.  Quantitative determinants of aerobic glycolysis identify flux through the enzyme GAPDH as a limiting step , 2014, eLife.

[46]  J. Blay,et al.  Targeting tumor-associated macrophages with anti-CSF-1R antibody reveals a strategy for cancer therapy. , 2014, Cancer cell.

[47]  S. Morrison,et al.  Infection mobilizes hematopoietic stem cells through cooperative NOD-like receptor and Toll-like receptor signaling. , 2014, Cell host & microbe.

[48]  C. Bing,et al.  Interleukin-1β mediates macrophage-induced impairment of insulin signaling in human primary adipocytes , 2014, American journal of physiology. Endocrinology and metabolism.

[49]  F. Powrie,et al.  Dysregulated Hematopoietic Stem and Progenitor Cell Activity Promotes Interleukin-23-Driven Chronic Intestinal Inflammation , 2012, Immunity.

[50]  N. Shime,et al.  C/EBPβ Is Involved in the Amplification of Early Granulocyte Precursors during Candidemia-Induced “Emergency” Granulopoiesis , 2012, The Journal of Immunology.

[51]  D. Glass,et al.  Cancer cachexia: mediators, signaling, and metabolic pathways. , 2012, Cell metabolism.

[52]  J. Olefsky,et al.  Neutrophils mediate insulin resistance in high fat diet fed mice via secreted elastase , 2012, Nature Medicine.

[53]  Daniel G. Anderson,et al.  Origins of tumor-associated macrophages and neutrophils , 2012, Proceedings of the National Academy of Sciences.

[54]  É. Azoulay,et al.  Survival in neutropenic patients with severe sepsis or septic shock* , 2012, Critical care medicine.

[55]  M. Tate,et al.  Depletion of Gr-1+, but not Ly6G+, immune cells exacerbates virus replication and disease in an intranasal model of herpes simplex virus type 1 infection. , 2010, The Journal of general virology.

[56]  C. Drake,et al.  Regulation of the IL-23 and IL-12 balance by Stat3 signaling in the tumor microenvironment. , 2009, Cancer cell.

[57]  B. Echtenacher,et al.  Murine Models of Anaemia of Inflammation: Extramedullary Haematopoiesis Represents a Species Specific Difference to Human Anaemia of Inflammation That Can Be Eliminated by Splenectomy , 2008, International journal of immunopathology and pharmacology.

[58]  Katerina Akassoglou,et al.  NF-κB links innate immunity to the hypoxic response through transcriptional regulation of HIF-1α , 2008, Nature.

[59]  David A. Cheresh,et al.  Nuclear cytokine-activated IKKα controls prostate cancer metastasis by repressing Maspin , 2007, Nature.

[60]  T. Hagemann,et al.  The inflammatory cytokine tumor necrosis factor-alpha generates an autocrine tumor-promoting network in epithelial ovarian cancer cells. , 2007, Cancer research.

[61]  Mark J. Ratain,et al.  Measuring response in a post-RECIST world: from black and white to shades of grey , 2006, Nature Reviews Cancer.

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

[63]  Pietro Ghezzi,et al.  Noncompetitive allosteric inhibitors of the inflammatory chemokine receptors CXCR1 and CXCR2: prevention of reperfusion injury. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[64]  V. Manganiello,et al.  Tumor necrosis factor-alpha stimulates lipolysis in differentiated human adipocytes through activation of extracellular signal-related kinase and elevation of intracellular cAMP. , 2002, Diabetes.

[65]  D. Kioussis,et al.  Transgenic mice expressing human tumour necrosis factor: a predictive genetic model of arthritis. , 1991, The EMBO journal.

[66]  E. Glaser The randomized clinical trial. , 1972, The New England journal of medicine.

[67]  C. Bozzini,et al.  Studies on medullary and extramedullary erythropoiesis in the adult mouse. , 1970, The American journal of physiology.

[68]  Otto Warburn,et al.  THE METABOLISM OF TUMORS , 1931 .

[69]  O. Warburg,et al.  THE METABOLISM OF TUMORS IN THE BODY , 1927, The Journal of general physiology.