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A Newly Licensed Peptide Presenter HLA-F: the Occurrence and the Prognostic Significance of this Cancer Immunoediting Molecule in Renal Cell Carcinoma and its Occurrence in Glioblastoma

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F18%3A00069189" target="_blank" >RIV/65269705:_____/18:00069189 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.nature.com/articles/labinvest201820" target="_blank" >https://www.nature.com/articles/labinvest201820</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/labinvest.2018.20" target="_blank" >10.1038/labinvest.2018.20</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A Newly Licensed Peptide Presenter HLA-F: the Occurrence and the Prognostic Significance of this Cancer Immunoediting Molecule in Renal Cell Carcinoma and its Occurrence in Glioblastoma

  • Original language description

    Among cancer immonoediting non-classical human leucocyte antigens (HLA) class Ib, HLA-F remains to be the most enigmatic. Originally it was thought to be specifically expressed only by extravillous trophoblast, which indicated its physiological role in a development of maternal tolerance to a semiallogeneic fetus (via engagement with inhibitory receptors on NK cells, mechanism also adopted by cancer cells to bypass host immunity). The expression by trophoblast was recently confirmed (Hackmon R 2017). Moreover, recently a peptide presenting function (presentation of peptides of unconventional length) was described in HLA-F (Dulberger CL 2017). Renal cell carcinoma (RCC) is characterized by its immunogenicity. Glioblastoma (GB) is a malignancy of an immune privileged site. An expression and prognostic significance of HLA-F by neoplastic cells in RCC and the expression in GB is not characterized. We evaluated the expression of HLA-F specific mRNA transcripts produced by neoplastic cells in 73 cases of RCC and in 54 samples of normal kidney parenchyma. We also evaluated expression of HLA-F molecule immunohistochemically in a pilot study of 24 cases of GB (IDH-wildtype in accordance with WHO 2016 revision). The results in RCC were statistically correlated with several clinicopathological parameters. We revealed that HLA-F is up-regulated in RCC (Tab.). On the other hand, its up-regulation is counterintuitively associated with prolonged disease-free survival (Fig. 1), more favorable pT stage and lower nuclear Fuhrmann&apos;s grade. In the pilot study of GB, we found cytoplasmic expression of HLA-F (Fig. 2) in 10 cases (42%). Because of a possibility of aberrant activation of expression of non-classical HLA molecules by interferons, the identification of HLA-F status could contribute to better selection of patients with RCC who could possibly benefit from more tailored neoadjuvant biological/immunological therapy. This molecule could represent useful prognostic biomarker in RCC. Non-classical molecule HLA-F, recently proven to be a peptide presenter, physiologically protects the fetus from maternal allorecognition. Our results suggest its role in cancer immunoediting in RCC and we proved its cytopasmic expression in 42% of cases of GB. Further studies appear warrantied.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30109 - Pathology

Result continuities

  • Project

    <a href="/en/project/NV17-32758A" target="_blank" >NV17-32758A: Imunopathologic mechanisms of the genesis, the course and therapy response in glioblastoma</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů