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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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    0333598 - ÚMG 2011 RIV DE eng J - Článek v odborném periodiku
    Šímová, Jana - Indrová, Marie - Bieblová, Jana - Mikyšková, Romana - Bubeník, Jan - Reiniš, Milan
    Therapy for minimal residual tumour disease: beta-galactosylceramide inhibits growth of recurrent HPV16-associated neoplasms after surgery and chemotherapy.
    International Journal of Cancer. Roč. 126, č. 12 (2010), s. 2997-3004. ISSN 0020-7136. E-ISSN 1097-0215
    Grant CEP: GA ČR GA301/06/0774; GA AV ČR IAA500520807; GA ČR GA301/07/1410; GA ČR GA301/09/1024
    GRANT EU: European Commission(XE) 18933 - CLINIGENE
    Výzkumný záměr: CEZ:AV0Z50520514
    Klíčová slova: beta-galactosylceramide * tumour immunotherapy * NKT cells
    Kód oboru RIV: EB - Genetika a molekulární biologie
    Impakt faktor: 4.926, rok: 2010

    This 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.
    Trvalý link: http://hdl.handle.net/11104/0178543

     
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