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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 ASEP 0333598 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Therapy for minimal residual tumour disease: beta-galactosylceramide inhibits growth of recurrent HPV16-associated neoplasms after surgery and chemotherapy Tvůrce(i) 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) RIDZdroj.dok. International Journal of Cancer. - : Wiley - ISSN 0020-7136
Roč. 126, č. 12 (2010), s. 2997-3004Poč.str. 2 s. Jazyk dok. eng - angličtina Země vyd. DE - Německo Klíč. slova beta-galactosylceramide ; tumour immunotherapy ; NKT cells Vědní obor RIV EB - Genetika a molekulární biologie CEP GA301/06/0774 GA ČR - Grantová agentura ČR IAA500520807 GA AV ČR - Akademie věd GA301/07/1410 GA ČR - Grantová agentura ČR GA301/09/1024 GA ČR - Grantová agentura ČR CEZ AV0Z50520514 - UMG-J (2005-2011) UT WOS 000277551100025 DOI 10.1002/ijc.24887 Anotace 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. Pracoviště Ústav molekulární genetiky Kontakt Nikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217 Rok sběru 2011
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