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A new dawn for eosinophils in the tumour microenvironment
- Source :
- Nature reviews. Cancer. 20(10)
- Publication Year :
- 2020
-
Abstract
- Eosinophils are evolutionarily conserved, pleotropic cells that display key effector functions in allergic diseases, such as asthma. Nonetheless, eosinophils infiltrate multiple tumours and are equipped to regulate tumour progression either directly by interacting with tumour cells or indirectly by shaping the tumour microenvironment (TME). Eosinophils can readily respond to diverse stimuli and are capable of synthesizing and secreting a large range of molecules, including unique granule proteins that can potentially kill tumour cells. Alternatively, they can secrete pro-angiogenic and matrix-remodelling soluble mediators that could promote tumour growth. Herein, we aim to comprehensively outline basic eosinophil biology that is directly related to their activity in the TME. We discuss the mechanisms of eosinophil homing to the TME and examine their diverse pro-tumorigenic and antitumorigenic functions. Finally, we present emerging data regarding eosinophils as predictive biomarkers and effector cells in immunotherapy, especially in response to immune checkpoint blockade therapy, and highlight outstanding questions for future basic and clinical cancer research.
- Subjects :
- General Mathematics
medicine.medical_treatment
Biology
03 medical and health sciences
0302 clinical medicine
Neoplasms
medicine
Tumor Microenvironment
Animals
Humans
Regulation of gene expression
Effector
Applied Mathematics
Disease Management
Chemotaxis
Immunotherapy
respiratory system
Eosinophil
Combined Modality Therapy
Immune checkpoint
Eosinophils
Gene Expression Regulation, Neoplastic
Chemotaxis, Leukocyte
medicine.anatomical_structure
030220 oncology & carcinogenesis
Cancer research
Disease Susceptibility
Signal transduction
Biomarkers
Homing (hematopoietic)
Signal Transduction
Subjects
Details
- ISSN :
- 14741768
- Volume :
- 20
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- Nature reviews. Cancer
- Accession number :
- edsair.doi.dedup.....11d8fd184caf4d6602792669eb4db076