Abstract

Upon activation, neutrophils release fibers composed of chromatin and neutrophil proteins termed neutrophil extracellular traps (NETs). NETs trap and kill microbes, activate dendritic cells and T cells, and are implicated in autoimmune and vascular diseases. Given the growing interest in the role of neutrophils in cancer immunoediting and the diverse function of NETs, we searched for NETs release by tumor-associated neutrophils (TANs). Using pediatric Ewing sarcoma (ES) as a model, we retrospectively examined histopathological material from diagnostic biopsies of eight patients (mean ± SD age of 11.5 ± 4.7 years). TANs were found in six patients and in two of those we identified NETs. These two patients presented with metastatic disease and despite entering complete remission after intensive chemotherapy had an early relapse. NETs were not identified in the diagnostic biopsies of two patients with localized disease and two with metastatic disease. This study is the first to show that TANs in ES are activated to make NETs, pointing to a possible role of NETs in cancer.

Highlights

  • Upon activation, neutrophils release neutrophil extracellular traps (NETs), which are fibers composed of chromatin and neutrophil proteins

  • This study is the first to show that tumor-associated neutrophils (TANs) in Ewing sarcoma (ES) are activated to make NETs, pointing to a possible role of NETs in cancer

  • This study is the first to show that TANs in ES are activated to make NETs and points to a possible role for NETs in cancer

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Summary

Introduction

Neutrophils release neutrophil extracellular traps (NETs), which are fibers composed of chromatin and neutrophil proteins. NETs are released via a novel form of cell death called NETosis (Brinkmann and Zychlinsky, 2012). Neutrophils release NETs that trap and kill microbes, activate dendritic cells (DCs) and T cells, and are implicated in autoimmune and vascular diseases(Brinkmann and Zychlinsky, 2012). We postulated that NETs have a role in cancer. The immune system can identify and destroy nascent tumor cells in a process termed cancer immunosurveillance. The immune system can promote tumor progression. There are no data on the possible role of NETs in this process

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