Identification and analysis of tumour-associated antigens in hepatocellular carcinoma

被引:0
|
作者
Y-Y Shi
H-C Wang
Y-H Yin
W-S Sun
Y Li
C-Q Zhang
Y Wang
S Wang
W-F Chen
机构
[1] Peking University Health Science Center,Immunology Department
[2] School of Medicine,Immunology Department
[3] Shandong University,Department II of Surgery and Laboratory of Surgical Oncology
[4] Sun Yat-Sen University Cancer Center,undefined
[5] Cancer Biological Therapy and Diagnosis Center,undefined
[6] Beijing Cancer Hospital,undefined
[7] Peking University People's Hospital,undefined
来源
British Journal of Cancer | 2005年 / 92卷
关键词
hepatocellular carcinoma; serological analysis of recombinant cDNA expression libraries; tumour antigens; cDNA microarray;
D O I
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中图分类号
学科分类号
摘要
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.
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页码:929 / 934
页数:5
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