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Identification and analysis of tumour-associated antigens in hepatocellular carcinoma
To identify tumour and tumour-associated antigens in patients with hepatocellular carcinoma (HCC) one may find potential diagnostic markers and immunotherapeutic targets. In the current study, 30 distinct antigens reactive with serum IgG from HCC patients were identified by serological analysis of c...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361901/ https://www.ncbi.nlm.nih.gov/pubmed/15756260 http://dx.doi.org/10.1038/sj.bjc.6602460 |
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author | Shi, Y-Y Wang, H-C Yin, Y-H Sun, W-S Li, Y Zhang, C-Q Wang, Y Wang, S Chen, W-F |
author_facet | Shi, Y-Y Wang, H-C Yin, Y-H Sun, W-S Li, Y Zhang, C-Q Wang, Y Wang, S Chen, W-F |
author_sort | Shi, Y-Y |
collection | PubMed |
description | To identify tumour and tumour-associated antigens in patients with hepatocellular carcinoma (HCC) one may find potential diagnostic markers and immunotherapeutic targets. In the current study, 30 distinct antigens reactive with serum IgG from HCC patients were identified by serological analysis of cDNA expression libraries (SEREX). The mRNA expression patterns of 14 of these 30 antigens were altered in cancer as further revealed by cDNA microarray, with upregulation for nine and downregulation for five antigens. One of the upregulated antigens was cancer-testis (CT) antigen (CAGE), which had been previously reported to be expressed exclusively in normal gametogenic tissues and aberrantly expressed in a variety of cancer cells. In our study, CAGE mRNA was expressed in 39.4% of HCC patients, 73.3% of patients with gastric cancer and 30.8% of patients with colorectal cancer. Antibodies against CAGE protein were detected in approximately 5.1% of the sera from HCC patients, 8.3% of that from gastric cancer patients and 7.3% of that from colorectal cancer patients. The relative high incidence of CAGE in cancer cells makes it a potential target for vaccine design. Another antigen of great interest is transgelin 2. The overexpression of transgelin 2 mRNA in a large per cent (69%) of HCC points to its potential as a diagnostic marker for HCC. |
format | Text |
id | pubmed-2361901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23619012009-09-10 Identification and analysis of tumour-associated antigens in hepatocellular carcinoma Shi, Y-Y Wang, H-C Yin, Y-H Sun, W-S Li, Y Zhang, C-Q Wang, Y Wang, S Chen, W-F Br J Cancer Molecular Diagnostics To identify tumour and tumour-associated antigens in patients with hepatocellular carcinoma (HCC) one may find potential diagnostic markers and immunotherapeutic targets. In the current study, 30 distinct antigens reactive with serum IgG from HCC patients were identified by serological analysis of cDNA expression libraries (SEREX). The mRNA expression patterns of 14 of these 30 antigens were altered in cancer as further revealed by cDNA microarray, with upregulation for nine and downregulation for five antigens. One of the upregulated antigens was cancer-testis (CT) antigen (CAGE), which had been previously reported to be expressed exclusively in normal gametogenic tissues and aberrantly expressed in a variety of cancer cells. In our study, CAGE mRNA was expressed in 39.4% of HCC patients, 73.3% of patients with gastric cancer and 30.8% of patients with colorectal cancer. Antibodies against CAGE protein were detected in approximately 5.1% of the sera from HCC patients, 8.3% of that from gastric cancer patients and 7.3% of that from colorectal cancer patients. The relative high incidence of CAGE in cancer cells makes it a potential target for vaccine design. Another antigen of great interest is transgelin 2. The overexpression of transgelin 2 mRNA in a large per cent (69%) of HCC points to its potential as a diagnostic marker for HCC. Nature Publishing Group 2005-03-14 2005-03-08 /pmc/articles/PMC2361901/ /pubmed/15756260 http://dx.doi.org/10.1038/sj.bjc.6602460 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Shi, Y-Y Wang, H-C Yin, Y-H Sun, W-S Li, Y Zhang, C-Q Wang, Y Wang, S Chen, W-F Identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
title | Identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
title_full | Identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
title_fullStr | Identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
title_full_unstemmed | Identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
title_short | Identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
title_sort | identification and analysis of tumour-associated antigens in hepatocellular carcinoma |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361901/ https://www.ncbi.nlm.nih.gov/pubmed/15756260 http://dx.doi.org/10.1038/sj.bjc.6602460 |
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