Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions
Extracellular vesicles (EVs) serve as trafficking vehicles and intercellular communication tools. Their cargo molecules directly reflect characteristics of their parental cell. This includes information on cell identity and specific cellular conditions, ranging from normal to pathological states. In...
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doaj-4cb692dd38fb4063a3a1b6964dd0d7fb2021-03-26T00:03:57ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-03-01223374337410.3390/ijms22073374Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune InteractionsSimone Lipinski0Katharina Tiemann1University Cancer Center Schleswig-Holstein (UCCSH), University Hospital Schleswig-Holstein, 24015 Kiel, GermanyInstitute for Hematopathology, Fangdieckstr. 75, 22547 Hamburg, GermanyExtracellular vesicles (EVs) serve as trafficking vehicles and intercellular communication tools. Their cargo molecules directly reflect characteristics of their parental cell. This includes information on cell identity and specific cellular conditions, ranging from normal to pathological states. In cancer, the content of EVs derived from tumor cells is altered and can induce oncogenic reprogramming of target cells. As a result, tumor-derived EVs compromise antitumor immunity and promote cancer progression and spreading. However, this pro-oncogenic phenotype is constantly being challenged by EVs derived from the local tumor microenvironment and from remote sources. Here, we summarize the role of EVs in the tumor–immune cross-talk that includes, but is not limited to, immune cells in the tumor microenvironment. We discuss the potential of remotely released EVs from the microbiome and during physical activity to shape the tumor–immune cross-talk, directly or indirectly, and confer antitumor activity. We further discuss the role of proinflammatory EVs in the temporal development of the tumor–immune interactions and their potential use for cancer diagnostics.https://www.mdpi.com/1422-0067/22/7/3374extracellular vesicletumor–immune microenvironmentmicrobiomephysical activitytumor evolutioninnate immune responses |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Simone Lipinski Katharina Tiemann |
spellingShingle |
Simone Lipinski Katharina Tiemann Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions International Journal of Molecular Sciences extracellular vesicle tumor–immune microenvironment microbiome physical activity tumor evolution innate immune responses |
author_facet |
Simone Lipinski Katharina Tiemann |
author_sort |
Simone Lipinski |
title |
Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions |
title_short |
Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions |
title_full |
Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions |
title_fullStr |
Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions |
title_full_unstemmed |
Extracellular Vesicles and Their Role in the Spatial and Temporal Expansion of Tumor–Immune Interactions |
title_sort |
extracellular vesicles and their role in the spatial and temporal expansion of tumor–immune interactions |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2021-03-01 |
description |
Extracellular vesicles (EVs) serve as trafficking vehicles and intercellular communication tools. Their cargo molecules directly reflect characteristics of their parental cell. This includes information on cell identity and specific cellular conditions, ranging from normal to pathological states. In cancer, the content of EVs derived from tumor cells is altered and can induce oncogenic reprogramming of target cells. As a result, tumor-derived EVs compromise antitumor immunity and promote cancer progression and spreading. However, this pro-oncogenic phenotype is constantly being challenged by EVs derived from the local tumor microenvironment and from remote sources. Here, we summarize the role of EVs in the tumor–immune cross-talk that includes, but is not limited to, immune cells in the tumor microenvironment. We discuss the potential of remotely released EVs from the microbiome and during physical activity to shape the tumor–immune cross-talk, directly or indirectly, and confer antitumor activity. We further discuss the role of proinflammatory EVs in the temporal development of the tumor–immune interactions and their potential use for cancer diagnostics. |
topic |
extracellular vesicle tumor–immune microenvironment microbiome physical activity tumor evolution innate immune responses |
url |
https://www.mdpi.com/1422-0067/22/7/3374 |
work_keys_str_mv |
AT simonelipinski extracellularvesiclesandtheirroleinthespatialandtemporalexpansionoftumorimmuneinteractions AT katharinatiemann extracellularvesiclesandtheirroleinthespatialandtemporalexpansionoftumorimmuneinteractions |
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