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Neutrophils Suppress Intraluminal NK Cell-Mediated Tumor Cell Clearance and Enhance Extravasation of Disseminated Carcinoma Cells.
Spiegel, Asaf; Brooks, Mary W; Houshyar, Samin; Reinhardt, Ferenc; Ardolino, Michele; Fessler, Evelyn; Chen, Michelle B; Krall, Jordan A; DeCock, Jasmine; Zervantonakis, Ioannis K; Iannello, Alexandre; Iwamoto, Yoshiko; Cortez-Retamozo, Virna; Kamm, Roger D; Pittet, Mikael J; Raulet, David H; Weinberg, Robert A.
Afiliação
  • Spiegel A; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • Brooks MW; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • Houshyar S; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • Reinhardt F; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • Ardolino M; Department of Molecular and Cell Biology and Cancer Research Laboratory, Division of Immunology, University of California at Berkeley, Berkeley, California.
  • Fessler E; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • Chen MB; Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
  • Krall JA; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • DeCock J; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts.
  • Zervantonakis IK; Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
  • Iannello A; Department of Molecular and Cell Biology and Cancer Research Laboratory, Division of Immunology, University of California at Berkeley, Berkeley, California.
  • Iwamoto Y; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Cortez-Retamozo V; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Kamm RD; Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
  • Pittet MJ; Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Raulet DH; Department of Molecular and Cell Biology and Cancer Research Laboratory, Division of Immunology, University of California at Berkeley, Berkeley, California.
  • Weinberg RA; Whitehead Institute for Biomedical Research, Cambridge, Massachusetts. Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts. Massachusetts Institute of Technology Ludwig Center for Molecular Oncology, Cambridge, Massachusetts. weinberg@wi.mit.edu.
Cancer Discov ; 6(6): 630-49, 2016 06.
Article em En | MEDLINE | ID: mdl-27072748
ABSTRACT
UNLABELLED Immune cells promote the initial metastatic dissemination of carcinoma cells from primary tumors. In contrast to their well-studied functions in the initial stages of metastasis, the specific roles of immunocytes in facilitating progression through the critical later steps of the invasion-metastasis cascade remain poorly understood. Here, we define novel functions of neutrophils in promoting intraluminal survival and extravasation at sites of metastatic dissemination. We show that CD11b(+)/Ly6G(+) neutrophils enhance metastasis formation via two distinct mechanisms. First, neutrophils inhibit natural killer cell function, which leads to a significant increase in the intraluminal survival time of tumor cells. Thereafter, neutrophils operate to facilitate extravasation of tumor cells through the secretion of IL1ß and matrix metalloproteinases. These results identify neutrophils as key regulators of intraluminal survival and extravasation through their cross-talk with host cells and disseminating carcinoma cells.

SIGNIFICANCE:

This study provides important insights into the systemic contributions of neutrophils to cancer metastasis by identifying how neutrophils facilitate intermediate steps of the invasion-metastasis cascade. We demonstrate that neutrophils suppress natural killer cell activity and increase extravasation of tumor cells. Cancer Discov; 6(6); 630-49. ©2016 AACR.This article is highlighted in the In This Issue feature, p. 561.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma / Células Matadoras Naturais / Neutrófilos Limite: Animals / Humans Idioma: En Revista: Cancer Discov Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma / Células Matadoras Naturais / Neutrófilos Limite: Animals / Humans Idioma: En Revista: Cancer Discov Ano de publicação: 2016 Tipo de documento: Article