Coexpression of MAGE-A peptides and HLA class I molecules in hepatocellular carcinoma.

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Coexpression of MAGE-A peptides and HLA class I molecules in hepatocellular carcinoma. / Roch, Nadine; Kutup, Asad; Vashist, Yogesh; Yekebas, Emre F.; Kalinin, Vjacheslav; Izbicki, Jakob R.

in: ANTICANCER RES, Jahrgang 30, Nr. 5, 5, 2010, S. 1617-1623.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Vancouver

Roch N, Kutup A, Vashist Y, Yekebas EF, Kalinin V, Izbicki JR. Coexpression of MAGE-A peptides and HLA class I molecules in hepatocellular carcinoma. ANTICANCER RES. 2010;30(5):1617-1623. 5.

Bibtex

@article{8d99193079ff44959721f083cc064d6f,
title = "Coexpression of MAGE-A peptides and HLA class I molecules in hepatocellular carcinoma.",
abstract = "Melanoma antigen (MAGE)-A derived peptides are tumour-specific and induce a strong in vitro T-cell response, if presented with human leukocyte antigen (HLA) molecules, which are involved in T-cell-mediated immune surveillance. MAGE-A-derived peptides are recognised by autologous cytotoxic T lymphocytes. The MAGE-A expression profile of hepatocellular carcinomas (HCC) was analysed by PCR assay covering MAGE-A transcripts in 13 patients. MAGE-A peptide expression was determined using a reverse transcription-PCR method. Cryostat sections were stained with monoclonal antibodies directed against HLA class I molecules. Twelve (92.3%) out of thirteen tumours expressed one MAGE-A gene. In at least 90% of the tumours, one MAGE-A peptide was expressed. Determination of the HLA status of the tumours showed a significant loss in approximately 40% of the tumours. The tumour-specific expression of MAGE genes and antigens encoded by a MAGE-family gene may represent useful targets for tumour-specific immunotherapy in HCC patients, in addition to established treatment options.",
author = "Nadine Roch and Asad Kutup and Yogesh Vashist and Yekebas, {Emre F.} and Vjacheslav Kalinin and Izbicki, {Jakob R.}",
year = "2010",
language = "Deutsch",
volume = "30",
pages = "1617--1623",
journal = "ANTICANCER RES",
issn = "0250-7005",
publisher = "International Institute of Anticancer Research",
number = "5",

}

RIS

TY - JOUR

T1 - Coexpression of MAGE-A peptides and HLA class I molecules in hepatocellular carcinoma.

AU - Roch, Nadine

AU - Kutup, Asad

AU - Vashist, Yogesh

AU - Yekebas, Emre F.

AU - Kalinin, Vjacheslav

AU - Izbicki, Jakob R.

PY - 2010

Y1 - 2010

N2 - Melanoma antigen (MAGE)-A derived peptides are tumour-specific and induce a strong in vitro T-cell response, if presented with human leukocyte antigen (HLA) molecules, which are involved in T-cell-mediated immune surveillance. MAGE-A-derived peptides are recognised by autologous cytotoxic T lymphocytes. The MAGE-A expression profile of hepatocellular carcinomas (HCC) was analysed by PCR assay covering MAGE-A transcripts in 13 patients. MAGE-A peptide expression was determined using a reverse transcription-PCR method. Cryostat sections were stained with monoclonal antibodies directed against HLA class I molecules. Twelve (92.3%) out of thirteen tumours expressed one MAGE-A gene. In at least 90% of the tumours, one MAGE-A peptide was expressed. Determination of the HLA status of the tumours showed a significant loss in approximately 40% of the tumours. The tumour-specific expression of MAGE genes and antigens encoded by a MAGE-family gene may represent useful targets for tumour-specific immunotherapy in HCC patients, in addition to established treatment options.

AB - Melanoma antigen (MAGE)-A derived peptides are tumour-specific and induce a strong in vitro T-cell response, if presented with human leukocyte antigen (HLA) molecules, which are involved in T-cell-mediated immune surveillance. MAGE-A-derived peptides are recognised by autologous cytotoxic T lymphocytes. The MAGE-A expression profile of hepatocellular carcinomas (HCC) was analysed by PCR assay covering MAGE-A transcripts in 13 patients. MAGE-A peptide expression was determined using a reverse transcription-PCR method. Cryostat sections were stained with monoclonal antibodies directed against HLA class I molecules. Twelve (92.3%) out of thirteen tumours expressed one MAGE-A gene. In at least 90% of the tumours, one MAGE-A peptide was expressed. Determination of the HLA status of the tumours showed a significant loss in approximately 40% of the tumours. The tumour-specific expression of MAGE genes and antigens encoded by a MAGE-family gene may represent useful targets for tumour-specific immunotherapy in HCC patients, in addition to established treatment options.

M3 - SCORING: Zeitschriftenaufsatz

VL - 30

SP - 1617

EP - 1623

JO - ANTICANCER RES

JF - ANTICANCER RES

SN - 0250-7005

IS - 5

M1 - 5

ER -