Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/15803
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dc.contributor.authorMirjacic Martinović K.-
dc.contributor.authorVuletić A.-
dc.contributor.authorMališić E.-
dc.contributor.authorSrdic-Rajic, Tatjana-
dc.contributor.authorTišma Miletić N.-
dc.contributor.authorBabovic N.-
dc.contributor.authorJurisic, Vladimir-
dc.date.accessioned2023-02-08T15:50:20Z-
dc.date.available2023-02-08T15:50:20Z-
dc.date.issued2022-
dc.identifier.issn0897-7194-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/15803-
dc.description.abstractTransforming growth factor beta (TGF-β) plays a complex role in carcinogenesis. In 30 melanoma patients and 20 healthy controls (HC) we analysed functional and phenotypic characteristics of NK cells by Flow cytometry, gene expression of TGF-β1 in peripheral blood mononuclear cells by qPCR and serum and supernatant level of free TGF-β1 by ELISA. Melanoma patients had significantly higher serum level of circulatingTGF-β1 compared to HC, especially those with metastasis into the central nervous system (subclass M1d) and high LDH serum values. Melanoma patients compared to HC had significantly higher level of TGF-β1 gene in PBMC. TGF-β1 serum values negatively correlate with NK cell activity analysed by CD107a (degranulation marker), IFN-γ, NKG2D, and NKp46 in patients. Study shows the association of high level of TGF-β1 with NK cell inhibition in patients represents the main mechanism of tumour immune evasion. Targeting TGF-β may become an important cancer treatment for improving antitumor immunity.-
dc.sourceGrowth Factors-
dc.titleIncreased circulating TGF-β1 is associated with impairment in NK cell effector functions in metastatic melanoma patients-
dc.typearticle-
dc.identifier.doi10.1080/08977194.2022.2124915-
dc.identifier.scopus2-s2.0-85139017368-
Appears in Collections:Faculty of Medical Sciences, Kragujevac

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