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Phenotype and function of tumor-associated neutrophils and their subsets in early-stage human lung cancer.
Eruslanov, Evgeniy B.
Afiliación
  • Eruslanov EB; Division of Thoracic Surgery, Department of Surgery, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, 6 Silverstein, Philadelphia, PA, 19104, USA. evgeniy.eruslanov@uphs.upenn.edu.
Cancer Immunol Immunother ; 66(8): 997-1006, 2017 Aug.
Article en En | MEDLINE | ID: mdl-28283697
ABSTRACT
Neutrophils accumulate in many types of human and murine tumors and represent a significant portion of tumor-infiltrating myeloid cells. Our current understanding of the role of neutrophils in tumor development has depended primarily on murine models of cancer. However, there are crucial species differences in the evolution of tumors, genetic diversity, immune and inflammatory responses, and intrinsic biology of neutrophils that might have a profound impact on the tumor development and function of neutrophils in mouse versus human tumors. To date, the majority of experimental approaches to study neutrophils in cancer patients have been limited to the examination of circulating blood neutrophils. The phenotype and function of tumor-associated neutrophils (TANs) in humans, particularly in the early stages of tumor development, have not been extensively investigated. Thus, the long-term goal of our work has been to characterize human TANs and determine their specific role in tumor development. Here, we summarize our findings on human TANs obtained from human early stage lung cancer patients. We will describe the phenotypes of different TAN subsets identified in early stage lung tumors, as well as their functional dialog with T cells.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Comunicación Celular / Escape del Tumor / Carcinogénesis / Neoplasias Pulmonares / Neutrófilos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Cancer Immunol Immunother Asunto de la revista: ALERGIA E IMUNOLOGIA / NEOPLASIAS / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Comunicación Celular / Escape del Tumor / Carcinogénesis / Neoplasias Pulmonares / Neutrófilos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Cancer Immunol Immunother Asunto de la revista: ALERGIA E IMUNOLOGIA / NEOPLASIAS / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos