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Myeloid-derived suppressor cells in prostate cancer: Present knowledge and future perspectives

Thumbnail
Autore
Koinis F., Xagara A., Chantzara E., Leontopoulou V., Aidarinis C., Kotsakis A.
Data
2022
Language
en
DOI
10.3390/cells11010020
Soggetto
amino acid transporter
chemokine receptor CXCR
cyclooxygenase 2 inhibitor
cytotoxic T lymphocyte antigen 4
fluorouracil
granulocyte macrophage colony stimulating factor
histone deacetylase inhibitor
interleukin 10
interleukin 23
interleukin 4
interleukin 5
interleukin 6
prostaglandin
prostaglandin E2
reactive nitrogen species
retinoic acid
STAT3 protein
stromal cell derived factor 1
taurursodiol
adaptive immunity
advanced cancer
antineoplastic activity
B lymphocyte
breast cancer
cancer associated fibroblast
cancer growth
cancer immunotherapy
cancer survival
CD8+ T lymphocyte
cell differentiation
cell function
cell infiltration
cell proliferation
clinical outcome
colon cancer
colorectal cancer
cytotoxic T lymphocyte
cytotoxicity
dendritic cell
disease exacerbation
endothelium cell
epithelial mesenchymal transition
fatty acid oxidation
fibroblast
head and neck cancer
human
human cell
immune response
immunosuppressive treatment
lung cancer
lymphoma
male
melanoma
mouse
myeloid-derived suppressor cell
natural killer cell
non small cell lung cancer
nonhuman
outcome assessment
ovary cancer
pancreas cancer
prostate cancer
regulatory T lymphocyte
Review
RNA sequence
sarcoma
T lymphocyte
Th17 cell
Th2 cell
thymoma
tumor associated leukocyte
tumor immunity
tumor microenvironment
tumor-associated macrophage
upregulation
immunology
immunotherapy
myeloid-derived suppressor cell
pathology
phenotype
prostate tumor
Humans
Immunosuppression Therapy
Immunotherapy
Male
Myeloid-Derived Suppressor Cells
Phenotype
Prostatic Neoplasms
Tumor Microenvironment
MDPI
Mostra tutti i dati dell'item
Abstract
Several lines of research are being investigated to better understand mechanisms implicated in response or resistance to immune checkpoint blockade in prostate cancer (PCa). Myeloid-derived suppressor cells (MDSCs) have emerged as a major mediator of immunosuppression in the tumor microenvironment that promotes progression of various tumor types. The main mechanisms under-lying MDSC-induced immunosuppression are currently being explored and strategies to enhance anti-tumor immune response via MDSC targeting are being tested. However, the role of MDSCs in PCa remains elusive. In this review, we aim to summarize and present the state-of-the-art knowledge on current methodologies to phenotypically and metabolically characterize MDSCs in PCa. We describe how these characteristics may be linked with MDSC function and may influence the clinical outcomes of patients with PCa. Finally, we briefly discuss emerging strategies being employed to therapeutically target MDSCs and potentiate the long-overdue improvement in the efficacy of immunotherapy in patients with PCa. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/74936
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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