Expression of the MAGE-1 gene in human hepatocellular carcinomas

To further investigate the expression of MAGE-1 gene in hepatocellular carcinoma (HCC). The tumors and adjacent liver tissue from 45 HCC patients and liver tissue from 28 non-HCC patients (16 with liver cirrhosis and 12 with normal liver) were characterized by RT-PCR. A 421 bp PCR product from a cDN...

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Veröffentlicht in:Chinese medical journal 2000-12, Vol.113 (12), p.1112-1118
Hauptverfasser: Chen, H, Cai, S, Wang, Y, Zhao, H, Peng, J, Pang, X, Zhu, J, Cong, X, Rui, J, Leng, X, Du, R, Vaughan, H, Cebon, J, Burgess, A W, Chen, W
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container_issue 12
container_start_page 1112
container_title Chinese medical journal
container_volume 113
creator Chen, H
Cai, S
Wang, Y
Zhao, H
Peng, J
Pang, X
Zhu, J
Cong, X
Rui, J
Leng, X
Du, R
Vaughan, H
Cebon, J
Burgess, A W
Chen, W
description To further investigate the expression of MAGE-1 gene in hepatocellular carcinoma (HCC). The tumors and adjacent liver tissue from 45 HCC patients and liver tissue from 28 non-HCC patients (16 with liver cirrhosis and 12 with normal liver) were characterized by RT-PCR. A 421 bp PCR product from a cDNA fragment spanning exons 1, 2 and 3 was sequenced. The HLA type was assayed by standard ELISA in 43 HCC patients. Thirty-two of 45 tumor tissues from HCC patients expressed MAGE-1 mRNA (71.1%). In contrast, MAGE-1 mRNA was not detected in adjacent tissues. Three were found to have point mutations at 3 identical sites resulting in the substitution of two amino acid residues. The most frequent HLA types in 43 HCC patients were: HLA-A2, 53.5%; A11, 25.6%; A24, 20.9%; A33, 20.9%; HLA-B13, 28.3% and B35, 23.2%. Expression of HLA-A33 (20.9%) was higher in HCC patients than that predicted in the normal Chinese population (8.8%). There was no discemable correlation between MAGE-1 expression and alpha-FP level, tumor size and hepatitis B or C virus infection. The identification of peptides which are restricted by haploptypes other than A1 should increase the opportunity for peptide based immunotherapy. This study shows that MAGE-1 mRNA is highly expressed in HCC tumor tissue in Chinese patients. Previously unreported point mutations in the MAGE-1 gene are described and may also provide additional opportunities for immunotherapy.
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The tumors and adjacent liver tissue from 45 HCC patients and liver tissue from 28 non-HCC patients (16 with liver cirrhosis and 12 with normal liver) were characterized by RT-PCR. A 421 bp PCR product from a cDNA fragment spanning exons 1, 2 and 3 was sequenced. The HLA type was assayed by standard ELISA in 43 HCC patients. Thirty-two of 45 tumor tissues from HCC patients expressed MAGE-1 mRNA (71.1%). In contrast, MAGE-1 mRNA was not detected in adjacent tissues. Three were found to have point mutations at 3 identical sites resulting in the substitution of two amino acid residues. The most frequent HLA types in 43 HCC patients were: HLA-A2, 53.5%; A11, 25.6%; A24, 20.9%; A33, 20.9%; HLA-B13, 28.3% and B35, 23.2%. Expression of HLA-A33 (20.9%) was higher in HCC patients than that predicted in the normal Chinese population (8.8%). There was no discemable correlation between MAGE-1 expression and alpha-FP level, tumor size and hepatitis B or C virus infection. The identification of peptides which are restricted by haploptypes other than A1 should increase the opportunity for peptide based immunotherapy. This study shows that MAGE-1 mRNA is highly expressed in HCC tumor tissue in Chinese patients. Previously unreported point mutations in the MAGE-1 gene are described and may also provide additional opportunities for immunotherapy.</description><identifier>ISSN: 0366-6999</identifier><identifier>PMID: 11776148</identifier><language>eng</language><publisher>China: Hepatology InstitutePeople’s Hospital,Peking University,Beijing 100044,China%DepartmentPeople’s Hospital,Peking University,Beijing 100044,China%School of Basic Medical Science,Liver Cancer Research Center,Peking University,Beijing 100083,China%Surgical DepartmentPeople’s Hospital,Peking University,Beijing 100044,China%Immunology Department,Peking University,Beijing 100083,China%Ludwig Institute for Cancer Research,Melbourne Branch,Australia</publisher><subject>Amino Acid Sequence ; Antigens, Neoplasm ; Base Sequence ; Binding Sites - genetics ; Carcinoma, Hepatocellular - genetics ; Carcinoma, Hepatocellular - pathology ; DNA, Complementary - chemistry ; DNA, Complementary - genetics ; Gene Expression Regulation, Neoplastic ; Haplotypes ; HLA Antigens - genetics ; HLA Antigens - metabolism ; Humans ; Liver Neoplasms - genetics ; Liver Neoplasms - pathology ; Melanoma-Specific Antigens ; Molecular Sequence Data ; Neoplasm Proteins - genetics ; Neoplasm Proteins - metabolism ; Protein Binding ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Sequence Analysis, DNA ; Tumor Cells, Cultured</subject><ispartof>Chinese medical journal, 2000-12, Vol.113 (12), p.1112-1118</ispartof><rights>Copyright © Wanfang Data Co. 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The identification of peptides which are restricted by haploptypes other than A1 should increase the opportunity for peptide based immunotherapy. This study shows that MAGE-1 mRNA is highly expressed in HCC tumor tissue in Chinese patients. Previously unreported point mutations in the MAGE-1 gene are described and may also provide additional opportunities for immunotherapy.</abstract><cop>China</cop><pub>Hepatology InstitutePeople’s Hospital,Peking University,Beijing 100044,China%DepartmentPeople’s Hospital,Peking University,Beijing 100044,China%School of Basic Medical Science,Liver Cancer Research Center,Peking University,Beijing 100083,China%Surgical DepartmentPeople’s Hospital,Peking University,Beijing 100044,China%Immunology Department,Peking University,Beijing 100083,China%Ludwig Institute for Cancer Research,Melbourne Branch,Australia</pub><pmid>11776148</pmid><tpages>7</tpages></addata></record>
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source MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Amino Acid Sequence
Antigens, Neoplasm
Base Sequence
Binding Sites - genetics
Carcinoma, Hepatocellular - genetics
Carcinoma, Hepatocellular - pathology
DNA, Complementary - chemistry
DNA, Complementary - genetics
Gene Expression Regulation, Neoplastic
Haplotypes
HLA Antigens - genetics
HLA Antigens - metabolism
Humans
Liver Neoplasms - genetics
Liver Neoplasms - pathology
Melanoma-Specific Antigens
Molecular Sequence Data
Neoplasm Proteins - genetics
Neoplasm Proteins - metabolism
Protein Binding
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - genetics
RNA, Messenger - metabolism
Sequence Analysis, DNA
Tumor Cells, Cultured
title Expression of the MAGE-1 gene in human hepatocellular carcinomas
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