Abstract

GENERAL COMMENTARY article Front. Oncol., 28 May 2015Sec. Molecular and Cellular Oncology Volume 5 - 2015 | https://doi.org/10.3389/fonc.2015.00118

Highlights

  • PTX3 is an extrinsic oncosuppressor regulating complement-dependent inflammation in cancer by Bonavita E, Gentile S, Rubino M, Maina V, Papait R, Kunderfranco P, et al Cell (2015) 160:700–14

  • Section of Pathology, Oncology and Experimental Biology, Department of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy

  • The tumor microenvironment (TME) is rich in inflammatory cells and inflammatory mediators that strongly affect tumor growth and progression as well as metastatic spreading. It has been known for a while that tumor-infiltrating inflammatory cells such as myeloid-derived suppressor cells (MDSCs) and tumor-associated macrophages (TAM) promote tumor growth, and several soluble factors, such as the CCL2 chemokine, the pro-inflammatory cytokines IL-1, IL-6, and TNFα, the pro-angiogenic factor VEGF are enriched in the TME (1)

Read more

Summary

Introduction

PTX3 is an extrinsic oncosuppressor regulating complement-dependent inflammation in cancer by Bonavita E, Gentile S, Rubino M, Maina V, Papait R, Kunderfranco P, et al Cell (2015) 160:700–14. PTX3 is produced locally, by macrophages and neutrophils and by endothelial and smooth muscle cells, in response to cytokines, pathogen-associated molecular patterns (PAMPs), intact microbes, oxidized-LDL, or HDL.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call