Abstract

Granulocyte colony-stimulating factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF) modulate progression of certain solid tumors. The G-CSF- or GM-CSF-secreting cancers, albeit not very common are, however, among the most rapidly advancing ones due to a cytokine-mediated immune suppression and angiogenesis. Similarly, de novo angiogenesis and vasculogenesis may complicate adjuvant use of recombinant G-CSF or GM-CSF thus possibly contributing to a cancer relapse. Rapid diagnostic tools to differentiate G-CSF- or GM-CSF-secreting cancers are not well developed therefore hindering efforts to individualize treatments for these patients. Given an increasing utilization of adjuvant G-/GM-CSF in cancer therapy, we aimed to summarize recent studies exploring their roles in pathophysiology of solid tumors and to provide insights into some complexities of their therapeutic applications.

Highlights

  • Granulocyte and granulocyte-macrophage colony-stimulating factors (G-CSF and GM-CSF, respectively) regulate maturation of progenitor cells in the bone marrow into differentiated granulocytes, macrophages, and the T cells

  • Cancer Medicine published by John Wiley & Sons Ltd

  • We aimed to present recent advances in studies addressing putative mechanisms and therapeutic uses of Granulocyte colony-stimulating factor (G-CSF) and GM-CSF in several cancers of a nonmyeloid origin

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Summary

Introduction

Granulocyte and granulocyte-macrophage colony-stimulating factors (G-CSF and GM-CSF, respectively) regulate maturation of progenitor cells in the bone marrow into differentiated granulocytes, macrophages, and the T cells. Recombinant G- or GM-CSFs are routinely used to correct neutropenia subsequent to chemotherapy and radiation. Adjuvant G-/GM-CSF treatments have been suggested to occasionally enable tumor growth. Such adverse treatment outcomes are thought to occur due to certain solid tumors being addicted to G-/GM-CSF-dependent signaling by expressing endogenous cytokines and/or their cognate receptors (G-/GM-CSFR). Clinical case reports reveal that newly diagnosed patients with G-/GM-CSF(R)-positive tumors a 2014 The Authors.

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