2022
DOI: 10.3390/cancers14164020
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Tumour Derived Extracellular Vesicles: Challenging Target to Blunt Tumour Immune Evasion

Abstract: Control of the immune response is crucial for tumour onset and progression. Tumour cells handle the immune reaction by means of secreted factors and extracellular vesicles (EV). Tumour-derived extracellular vesicles (TEV) play key roles in immune reprogramming by delivering their cargo to different immune cells. Tumour-surrounding tissues also contribute to tumour immune editing and evasion, tumour progression, and drug resistance via locally released TEV. Moreover, the increase in circulating TEV has suggeste… Show more

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Cited by 7 publications
(3 citation statements)
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“…The extracellular Hsp70 may bind to specific receptor CD19 of dendritic cells (DCs), then DCs presented antigen by MHC-I to T-cytotoxic cells and induce many pro-inflammatory like IL-1 and TNFα. ExHsp70 may bind non-specifically to dendritic cells, leading to antigen presentation by MHC-II to T-helper cells and the induction of an anti-inflammatory cytokine like IL-10 [25]. Hulina and colleagues in 2018 demonstrated that exHsp70 can induce IL-1α secretion in THP-1 cells, a human leukemia monocytic cell line widely used to assess macrophage activity modulation (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The extracellular Hsp70 may bind to specific receptor CD19 of dendritic cells (DCs), then DCs presented antigen by MHC-I to T-cytotoxic cells and induce many pro-inflammatory like IL-1 and TNFα. ExHsp70 may bind non-specifically to dendritic cells, leading to antigen presentation by MHC-II to T-helper cells and the induction of an anti-inflammatory cytokine like IL-10 [25]. Hulina and colleagues in 2018 demonstrated that exHsp70 can induce IL-1α secretion in THP-1 cells, a human leukemia monocytic cell line widely used to assess macrophage activity modulation (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Recent studies have revealed that TDEVs can reprogram cancer-infiltrated dendritic cells (DCs) toward a tumor-promoting phenotype, thereby mediating tumor immune suppression. 293 The maturation and function of DC cells depend on the composition of their contents, but TDEVs content, including HSP, TLR, HLA g, 294 S100A8, S100A9, Annexin A1, 292 PGE2, 295 TGFβ1, 296 or miRs, 297 suppress DC maturation. Normal and tumor-derived EVs have been shown to carry and transfer proteins, lipids, and nucleic acids to neighboring cells.…”
Section: Sources Of Extracellular Vesiclesmentioning
confidence: 99%
“…However, stem cell-based therapies have their disadvantages. More than 99% of the implanted stem cells are trapped in the spleen, lung, and liver, while those cells close to the target tissues have a short life span and are prone to thrombosis, fever, and tumors [ 7 , 8 , 9 , 10 , 11 ]. Although this use of stem cells in combination with various scaffolds has long solved this problem, stem cells are still prone to cause oxidative stress and immune responses [ 12 , 13 ].…”
Section: Introductionmentioning
confidence: 99%