id paper:paper_09527915_v45_n_p8_MendezHuergo
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spelling paper:paper_09527915_v45_n_p8_MendezHuergo2023-06-08T15:55:03Z Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis galectin glycan galectin bone marrow cell carcinogenesis CD4+ T lymphocyte cell differentiation gene expression profiling glioblastoma glycosylation human immunomodulation immunoregulation internalization Kaposi sarcoma natural killer cell oligomerization protein binding protein domain protein protein interaction regulatory T lymphocyte Review signal transduction T lymphocyte tumor associated leukocyte tumor immunity animal immunology neoplasm neovascularization (pathology) pathology vascularization Animals Galectins Humans Killer Cells, Natural Neoplasms Neovascularization, Pathologic T-Lymphocytes Immune checkpoints, a plethora of inhibitory pathways aimed at maintaining immune cell homeostasis, may be co-opted by cancer cells to evade immune destruction. Therapies targeting immune checkpoints have reached a momentum yielding significant clinical benefits in patients with various malignancies by unleashing anti-tumor immunity. Galectins, a family of glycan-binding proteins, have emerged as novel regulatory checkpoints that promote immune evasive programs by inducing T-cell exhaustion, limiting T-cell survival, favoring expansion of regulatory T cells, de-activating natural killer cells and polarizing myeloid cells toward an immunosuppressive phenotype. Concomitantly, galectins can trigger vascular signaling programs, serving as bifunctional messengers that couple tumor immunity and angiogenesis. Thus, targeting galectin–glycan interactions may halt tumor progression by simultaneously augmenting antitumor immunity and suppressing aberrant angiogenesis. © 2017 Elsevier Ltd 2017 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09527915_v45_n_p8_MendezHuergo http://hdl.handle.net/20.500.12110/paper_09527915_v45_n_p8_MendezHuergo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic galectin
glycan
galectin
bone marrow cell
carcinogenesis
CD4+ T lymphocyte
cell differentiation
gene expression profiling
glioblastoma
glycosylation
human
immunomodulation
immunoregulation
internalization
Kaposi sarcoma
natural killer cell
oligomerization
protein binding
protein domain
protein protein interaction
regulatory T lymphocyte
Review
signal transduction
T lymphocyte
tumor associated leukocyte
tumor immunity
animal
immunology
neoplasm
neovascularization (pathology)
pathology
vascularization
Animals
Galectins
Humans
Killer Cells, Natural
Neoplasms
Neovascularization, Pathologic
T-Lymphocytes
spellingShingle galectin
glycan
galectin
bone marrow cell
carcinogenesis
CD4+ T lymphocyte
cell differentiation
gene expression profiling
glioblastoma
glycosylation
human
immunomodulation
immunoregulation
internalization
Kaposi sarcoma
natural killer cell
oligomerization
protein binding
protein domain
protein protein interaction
regulatory T lymphocyte
Review
signal transduction
T lymphocyte
tumor associated leukocyte
tumor immunity
animal
immunology
neoplasm
neovascularization (pathology)
pathology
vascularization
Animals
Galectins
Humans
Killer Cells, Natural
Neoplasms
Neovascularization, Pathologic
T-Lymphocytes
Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
topic_facet galectin
glycan
galectin
bone marrow cell
carcinogenesis
CD4+ T lymphocyte
cell differentiation
gene expression profiling
glioblastoma
glycosylation
human
immunomodulation
immunoregulation
internalization
Kaposi sarcoma
natural killer cell
oligomerization
protein binding
protein domain
protein protein interaction
regulatory T lymphocyte
Review
signal transduction
T lymphocyte
tumor associated leukocyte
tumor immunity
animal
immunology
neoplasm
neovascularization (pathology)
pathology
vascularization
Animals
Galectins
Humans
Killer Cells, Natural
Neoplasms
Neovascularization, Pathologic
T-Lymphocytes
description Immune checkpoints, a plethora of inhibitory pathways aimed at maintaining immune cell homeostasis, may be co-opted by cancer cells to evade immune destruction. Therapies targeting immune checkpoints have reached a momentum yielding significant clinical benefits in patients with various malignancies by unleashing anti-tumor immunity. Galectins, a family of glycan-binding proteins, have emerged as novel regulatory checkpoints that promote immune evasive programs by inducing T-cell exhaustion, limiting T-cell survival, favoring expansion of regulatory T cells, de-activating natural killer cells and polarizing myeloid cells toward an immunosuppressive phenotype. Concomitantly, galectins can trigger vascular signaling programs, serving as bifunctional messengers that couple tumor immunity and angiogenesis. Thus, targeting galectin–glycan interactions may halt tumor progression by simultaneously augmenting antitumor immunity and suppressing aberrant angiogenesis. © 2017 Elsevier Ltd
title Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
title_short Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
title_full Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
title_fullStr Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
title_full_unstemmed Galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
title_sort galectins: emerging regulatory checkpoints linking tumor immunity and angiogenesis
publishDate 2017
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09527915_v45_n_p8_MendezHuergo
http://hdl.handle.net/20.500.12110/paper_09527915_v45_n_p8_MendezHuergo
_version_ 1768544874560225280