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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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. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/zhcmj/zhcmj.jpg</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11776148$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, H</creatorcontrib><creatorcontrib>Cai, S</creatorcontrib><creatorcontrib>Wang, Y</creatorcontrib><creatorcontrib>Zhao, H</creatorcontrib><creatorcontrib>Peng, J</creatorcontrib><creatorcontrib>Pang, X</creatorcontrib><creatorcontrib>Zhu, J</creatorcontrib><creatorcontrib>Cong, X</creatorcontrib><creatorcontrib>Rui, J</creatorcontrib><creatorcontrib>Leng, X</creatorcontrib><creatorcontrib>Du, R</creatorcontrib><creatorcontrib>Vaughan, H</creatorcontrib><creatorcontrib>Cebon, J</creatorcontrib><creatorcontrib>Burgess, A W</creatorcontrib><creatorcontrib>Chen, W</creatorcontrib><title>Expression of the MAGE-1 gene in human hepatocellular carcinomas</title><title>Chinese medical journal</title><addtitle>Chin Med J (Engl)</addtitle><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.</description><subject>Amino Acid Sequence</subject><subject>Antigens, Neoplasm</subject><subject>Base Sequence</subject><subject>Binding Sites - genetics</subject><subject>Carcinoma, Hepatocellular - genetics</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>DNA, Complementary - chemistry</subject><subject>DNA, Complementary - genetics</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Haplotypes</subject><subject>HLA Antigens - genetics</subject><subject>HLA Antigens - metabolism</subject><subject>Humans</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - pathology</subject><subject>Melanoma-Specific Antigens</subject><subject>Molecular Sequence Data</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Protein Binding</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Sequence Analysis, DNA</subject><subject>Tumor Cells, Cultured</subject><issn>0366-6999</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkD1PwzAYhD2AaCn8BeSJLdLr2LGTjaoKBamIBebIcV63qRI72In4-PUEUcRytzy6O90ZWQKXMpFFUSzIZYxHgDTLlLwgC8aUkkzkS3JXfgwBY2y9o97S8YD0ab0tE0b36JC2jh6mXs-Kgx69wa6bOh2o0cG0zvc6XpFzq7uI1ydfkdf78mXzkOyet4-b9S4ZUp6PCVoNgEJwI7nJLDSpttJwW6fcSmhMjoLnwLgsWF3UQhsphDCI0CBYVBlfkdvf3HftrHb76uin4ObG6utg-mMKACwFJv7BIfi3CeNY9W38Ga4d-ilWCjKmhFAzeHMCp7rHphpC2-vwWf2dw78BX_BeZg</recordid><startdate>20001201</startdate><enddate>20001201</enddate><creator>Chen, H</creator><creator>Cai, S</creator><creator>Wang, Y</creator><creator>Zhao, H</creator><creator>Peng, J</creator><creator>Pang, X</creator><creator>Zhu, J</creator><creator>Cong, X</creator><creator>Rui, J</creator><creator>Leng, X</creator><creator>Du, R</creator><creator>Vaughan, H</creator><creator>Cebon, J</creator><creator>Burgess, A W</creator><creator>Chen, W</creator><general>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</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20001201</creationdate><title>Expression of the MAGE-1 gene in human hepatocellular carcinomas</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p238t-efa00e443c63c5f0d2af6c3fb23f60dc8e438013691b9b4ac6444cee0de0fe753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Amino Acid Sequence</topic><topic>Antigens, Neoplasm</topic><topic>Base Sequence</topic><topic>Binding Sites - genetics</topic><topic>Carcinoma, Hepatocellular - genetics</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>DNA, Complementary - chemistry</topic><topic>DNA, Complementary - genetics</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Haplotypes</topic><topic>HLA Antigens - genetics</topic><topic>HLA Antigens - metabolism</topic><topic>Humans</topic><topic>Liver Neoplasms - genetics</topic><topic>Liver Neoplasms - pathology</topic><topic>Melanoma-Specific Antigens</topic><topic>Molecular Sequence Data</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Protein Binding</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Sequence Analysis, DNA</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, H</creatorcontrib><creatorcontrib>Cai, S</creatorcontrib><creatorcontrib>Wang, Y</creatorcontrib><creatorcontrib>Zhao, H</creatorcontrib><creatorcontrib>Peng, J</creatorcontrib><creatorcontrib>Pang, X</creatorcontrib><creatorcontrib>Zhu, J</creatorcontrib><creatorcontrib>Cong, X</creatorcontrib><creatorcontrib>Rui, J</creatorcontrib><creatorcontrib>Leng, X</creatorcontrib><creatorcontrib>Du, R</creatorcontrib><creatorcontrib>Vaughan, H</creatorcontrib><creatorcontrib>Cebon, J</creatorcontrib><creatorcontrib>Burgess, A W</creatorcontrib><creatorcontrib>Chen, W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, H</au><au>Cai, S</au><au>Wang, Y</au><au>Zhao, H</au><au>Peng, J</au><au>Pang, X</au><au>Zhu, J</au><au>Cong, X</au><au>Rui, J</au><au>Leng, X</au><au>Du, R</au><au>Vaughan, H</au><au>Cebon, J</au><au>Burgess, A W</au><au>Chen, W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of the MAGE-1 gene in human hepatocellular carcinomas</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chin Med J (Engl)</addtitle><date>2000-12-01</date><risdate>2000</risdate><volume>113</volume><issue>12</issue><spage>1112</spage><epage>1118</epage><pages>1112-1118</pages><issn>0366-6999</issn><abstract>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.</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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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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