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Therapy for minimal residual tumour disease: beta-galactosylceramide inhibits growth of recurrent HPV16-associated neoplasms after surgery and chemotherapy

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    SYSNO ASEP0333598
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTherapy for minimal residual tumour disease: beta-galactosylceramide inhibits growth of recurrent HPV16-associated neoplasms after surgery and chemotherapy
    Author(s) Šímová, Jana (UMG-J) RID
    Indrová, Marie (UMG-J) RID
    Bieblová, Jana (UMG-J)
    Mikyšková, Romana (UMG-J) RID
    Bubeník, Jan (UMG-J)
    Reiniš, Milan (UMG-J) RID
    Source TitleInternational Journal of Cancer. - : Wiley - ISSN 0020-7136
    Roč. 126, č. 12 (2010), s. 2997-3004
    Number of pages2 s.
    Languageeng - English
    CountryDE - Germany
    Keywordsbeta-galactosylceramide ; tumour immunotherapy ; NKT cells
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGA301/06/0774 GA ČR - Czech Science Foundation (CSF)
    IAA500520807 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GA301/07/1410 GA ČR - Czech Science Foundation (CSF)
    GA301/09/1024 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000277551100025
    DOI10.1002/ijc.24887
    AnnotationThis study was focused on tumour-inhibitory effects of 12 carbon acyl chain beta-galactosylceramide (C12 beta-D-GalactosylCeramide) on the growth of HPV16-associated neoplasms transplanted in syngeneic mice. Treatment of tumour-bearing mice with beta-galactosylceramide 3-14 days after tumour cell transplantation significantly inhibited growth of the MHC class I-positive (TC-1), as well as MHC class I-deficient (TC-1/A9) HPV16-asssociated tumours. Administration of beta-galactosylceramide after surgical removal of TC-1 tumours inhibited growth of tumour recurrences. Similar results were obtained in the treatment of the tumours after chemotherapy. Beta-galactosylceramide treatment turned out to be also synergistic with immunotherapy based on administration of IL-12-producing cellular vaccines. These results suggest that beta-galactosylceramide can be effective for treatment of minimal residual tumour disease as well as an adjuvant for cancer immunotherapy.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2011
Number of the records: 1  

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