Premetastatic soil and prevention of breast cancer brain metastasis

Neuro Oncol. 2013 Jul;15(7):891-903. doi: 10.1093/neuonc/not031. Epub 2013 Apr 17.

Abstract

Background: As therapies for systemic cancer improve and patients survive longer, the risk for brain metastases increases. We evaluated whether immune mechanisms are involved in the development of brain metastasis.

Methods: We conducted our studies using BALB/c mice bearing syngeneic 4T1 mammary adenocarcinoma cells in the mammary gland.

Results: The brains of mice bearing 4T1 tumors at day 14 had no detectable metastatic tumor cells but presented with marked accumulation of bone marrow-derived CD11b(+)Gr1(+) myeloid cells, which express high levels of inflammatory chemokines S100A8 and S100A9. In vitro, S100A9 attracts 4T1 cells through Toll-like receptor 4 and CD11b(+)Gr1(+) myeloid cells through Toll-like receptor 4 and the receptor for advanced glycation end-products. Systemic treatment of 4T1-bearing mice with anti-Gr1 (RB6-8C5) monoclonal antibody reduces accumulation of CD11b(+)Gr1(+) myeloid cells in the day-14 premetastatic brain as well as subsequent brain metastasis of 4T1 cells detected on day 30. Furthermore, treatment of 4T1 tumor-bearing mice with the cyclooxygenase-2 inhibitor celecoxib or genetic disruption of cyclooxygenase-2 in 4T1 cells inhibits the inflammatory chemokines and infiltration of CD11b(+)Gr1(+) myeloid cells in the premetastatic brain and subsequent formation of brain metastasis.

Conclusions: Our results suggest that the primary tumor induces accumulation of CD11b(+)Gr1(+) myeloid cells in the brain to form "premetastatic soil" and inflammation mediators, such as S100A9, that attract additional myeloid cells as well as metastatic tumor cells. Celecoxib and anti-Gr1 treatment may be useful for blockade of these processes, thereby preventing brain metastasis in patients with breast cancer.

Keywords: CCL2; S100A8/A9; brain metastasis; breast cancer; myeloid-derived suppressor cells; prostaglandin-E2.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Adenocarcinoma / prevention & control*
  • Animals
  • Apoptosis / drug effects
  • Blotting, Western
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / prevention & control*
  • Brain Neoplasms / secondary
  • CD11b Antigen / genetics
  • CD11b Antigen / metabolism*
  • Calgranulin B / genetics
  • Calgranulin B / metabolism
  • Celecoxib
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cyclooxygenase 2 / chemistry
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Cyclooxygenase 2 Inhibitors / pharmacology
  • Female
  • Flow Cytometry
  • Green Fluorescent Proteins / metabolism
  • Immunoenzyme Techniques
  • Inflammation Mediators / metabolism
  • Leukocytes / cytology
  • Leukocytes / drug effects
  • Leukocytes / metabolism
  • Mammary Neoplasms, Experimental / metabolism
  • Mammary Neoplasms, Experimental / pathology
  • Mammary Neoplasms, Experimental / prevention & control*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Mice, Transgenic
  • Myeloid Cells / drug effects
  • Myeloid Cells / metabolism
  • Myeloid Cells / pathology*
  • Pyrazoles / pharmacology
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sulfonamides / pharmacology
  • Tumor Cells, Cultured

Substances

  • CD11b Antigen
  • Calgranulin B
  • Cyclooxygenase 2 Inhibitors
  • Gr-1 protein, mouse
  • Inflammation Mediators
  • Pyrazoles
  • RNA, Messenger
  • Receptors, Chemokine
  • S100A9 protein, mouse
  • Sulfonamides
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Celecoxib