Abstract
Primary tumors have been shown to prepare distal organs for later colonization of metastatic cells by stimulating organ-specific infiltration of bone marrow derived cells. Here we demonstrate that neutrophils accumulate in the lung prior to the arrival of metastatic cells in mouse models of breast cancer. Tumor-entrained neutrophils (TENs) inhibit metastatic seeding in the lungs by generating H(2)O(2) and tumor secreted CCL2 is a critical mediator of optimal antimetastatic entrainment of G-CSF-stimulated neutrophils. TENs are present in the peripheral blood of breast cancer patients prior to surgical resection but not in healthy individuals. Thus, whereas tumor-secreted factors contribute to tumor progression at the primary site, they concomitantly induce a neutrophil-mediated inhibitory process at the metastatic site.
Copyright © 2011 Elsevier Inc. All rights reserved.
Publication types
-
Research Support, N.I.H., Extramural
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Bone Marrow Cells
-
Breast Neoplasms / immunology
-
Breast Neoplasms / pathology*
-
Cell Line, Tumor
-
Chemokine CCL2 / metabolism
-
Cytotoxicity, Immunologic
-
Female
-
Granulocyte Colony-Stimulating Factor / metabolism
-
Humans
-
Hydrogen Peroxide / metabolism
-
Lung / immunology*
-
Lung / pathology
-
Lung Neoplasms / immunology
-
Lung Neoplasms / pathology
-
Lung Neoplasms / secondary*
-
Mice
-
Mice, Inbred BALB C
-
Mice, Inbred C57BL
-
Molecular Sequence Data
-
Neoplasm Invasiveness
-
Neutrophils / immunology*
-
Neutrophils / metabolism*
-
RNA Interference
-
RNA, Small Interfering
-
Reactive Oxygen Species / metabolism
-
Transforming Growth Factor beta / metabolism
Substances
-
Ccl2 protein, mouse
-
Chemokine CCL2
-
RNA, Small Interfering
-
Reactive Oxygen Species
-
Transforming Growth Factor beta
-
Granulocyte Colony-Stimulating Factor
-
Hydrogen Peroxide