Skip to main content

Polymorphonuclear Neutrophils and Tumors: Friend or Foe?

  • Chapter
  • First Online:
Interaction of Immune and Cancer Cells

Part of the book series: Experientia Supplementum ((EXS,volume 113))

Abstract

Tumor microenvironment (TME) is a dynamic network that apart from tumor cells includes also cells of the immune system, e.g., neutrophils, which are recruited from blood circulation. In TME, neutrophils are strongly implicated in the direct and indirect interactions with tumor cells or other immune cells, and they play roles in both preventing and/or facilitating tumor progression and metastasis. The dual role of neutrophils is determined by their high plasticity and heterogeneity. Analogous to the macrophages, neutrophils can express antitumoral (N1) and protumoral (N2) phenotypes which differ substantially in morphology and function. N1 phenotype characterizes with a high cytotoxic and proinflammatory activities, while N2 phenotype with immunosuppressive and prometastatic properties. The antitumoral effect of neutrophils includes for example the production of reactive oxygen species or proapoptotic molecules. The protumoral action of neutrophils relies on releasing of proangiogenic and prometastatic mediators, immunosuppressive factors, as well as on direct helping tumor cells in extravasation process. This chapter summarizes the heterogeneity of neutrophils in TME, as well as their dual role on tumor cells.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 149.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 199.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 199.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Abbreviations

ADCC:

Antibody-dependent cell-mediated cytotoxicity

ARG-1:

Arginase 1

BMs:

Basement membranes

CG:

Cathepsin G

CTCs:

Circulatory tumor cells

ECM:

Extracellular matrix

EMT:

Epithelial–mesenchymal transition

FGF:

Fibroblast growth factor

G-CSF:

Granulocyte colony-stimulating factor

GM-CSF:

Granulocyte-macrophage colony-stimulating factor

HDNs:

High density neutrophils

huGCP-2:

Human granulocyte chemotactic protein 2

ICAM-1:

Intracellular adhesion molecule 1

IFN:

Interferon

IL:

Interleukin

IRS-1:

Insulin receptor substrate-1

LDNs:

Low-density neutrophils

LFA-1:

Lymphocyte function-associated antigen 1

LPS:

Lipopolysaccharide

MAPKs:

Mitogen-activated protein kinases

MIP-1 α:

Macrophage inflammatory protein-1 α

MMPs:

Metalloproteinases

NE:

Neutrophil elastase

NETs:

Neutrophil extracellular traps

NK:

Natural killer

OSM:

Oncostatin M

PD-1:

Programmed cell death protein 1

PD-L1:

Ligand for programmed cell death protein 1

PI3K:

Phosphoinositide-3 kinase

PMA:

Phorbol-12-myristate-13-acetate

ROS:

Reactive oxygen species

sLeX:

Sialyl Lewis X

TAMs:

Tumor-associated macrophages

TANs:

Tumor-associated neutrophils

TGF-β:

Transforming growth factor β

TLR:

Toll-like receptor

TME:

Tumor microenvironment

TNF-α:

Tumor necrosis factor-α

TRAIL:

TNF-Related apoptosis-inducing ligand

VEGF:

Vascular endothelial growth factor

References

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Magdalena Klink .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2022 The Author(s), under exclusive license to Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Szulc-Kielbik, I., Klink, M. (2022). Polymorphonuclear Neutrophils and Tumors: Friend or Foe?. In: Klink, M., Szulc-Kielbik, I. (eds) Interaction of Immune and Cancer Cells. Experientia Supplementum, vol 113. Springer, Cham. https://doi.org/10.1007/978-3-030-91311-3_5

Download citation

Publish with us

Policies and ethics