2016
DOI: 10.1016/j.taap.2016.06.020
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Smoking-related microRNAs and mRNAs in human peripheral blood mononuclear cells

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Cited by 18 publications
(18 citation statements)
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“…Together with miR-6086 and miR-6088, miR-6087 is found at high levels in undifferentiated embryonic stem cells, and their expression is lowered during endothelial differentiation (45). Other miRNAs relevant for melanoma pathogenesis include miR-4498, which was isolated at higher levels from hypoxic exosomes and might influence immune responses by targeting CD83, an immunostimulatory molecule critical for the activation of T-cells (46). miR-21, which we found in both normoxic and hypoxic exosomes, was described as promoting a pro-metastatic phenotype when delivered to normoxic oral squamous cell carcinoma cells by increasing snail family transcriptional repressor 1 (SNAI1) and vimentin expression (47).…”
Section: Discussionmentioning
confidence: 99%
“…Together with miR-6086 and miR-6088, miR-6087 is found at high levels in undifferentiated embryonic stem cells, and their expression is lowered during endothelial differentiation (45). Other miRNAs relevant for melanoma pathogenesis include miR-4498, which was isolated at higher levels from hypoxic exosomes and might influence immune responses by targeting CD83, an immunostimulatory molecule critical for the activation of T-cells (46). miR-21, which we found in both normoxic and hypoxic exosomes, was described as promoting a pro-metastatic phenotype when delivered to normoxic oral squamous cell carcinoma cells by increasing snail family transcriptional repressor 1 (SNAI1) and vimentin expression (47).…”
Section: Discussionmentioning
confidence: 99%
“…The immunosuppressive effect was mediated by miR-23a, in addition to TGF-β (Berchem et al 2015). MiR-4498 showed higher levels in hypoxic exosomes isolated from melanoma cells (own unpublished results) and might influence immune responses by targeting CD83, an immunostimulatory molecule critical for the activation of T cells (Su et al 2016). In murine tumor models, mir-494 was shown to regulate the activity of MDSC (myeloid-derived suppressor cells), a major type of immunosuppressive cells (Liu et al 2012).…”
Section: The Functions Of Cancer-derived Exosomes In Immunosuppressionmentioning
confidence: 99%
“…A similar activity was attributed to miR-494 that inhibited macrophage polarization and switched them towards the immunosuppressive M2 type (Zhao et al 2016). In a co-culture system of murine cell lines, pancreatic cancer cell-derived exosomes shifted macrophage polarization to the M2 phenotype (Su et al 2016). Over-expression of miR-155 and miR-125b-2 in the cancer cells reverted this effect and resulted in M1 polarized macrophages upon exosome exposure.…”
Section: The Functions Of Cancer-derived Exosomes In Immunosuppressionmentioning
confidence: 99%
“…In addition, increased levels of miR-4498 were observed in hypoxic T-EVs derived from melanoma cells [ 35 ]. CD83, which is a key in the communication between cells of the innate and adaptive immune response, is regulated by miR-4498 [ 56 ].…”
Section: Immunosuppression By Cancer-derived Extracellular Vesiclesmentioning
confidence: 99%