Quantitative evaluation of the expression of MAGE genes in tumors by limiting dilution of cDNA libraries.

Details

Serval ID
serval:BIB_10546
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Quantitative evaluation of the expression of MAGE genes in tumors by limiting dilution of cDNA libraries.
Journal
International Journal of Cancer
Author(s)
Serrano A., Lethé B., Delroisse J.M., Lurquin C., De Plaen E., Brasseur F., Rimoldi D., Boon T.
ISSN
0020-7136 (Print)
ISSN-L
0020-7136
Publication state
Published
Issued date
1999
Volume
83
Number
5
Pages
664-669
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
The MAGE-A genes are expressed in tumor cells but not in healthy tissues, except in male germ line cells and in placenta. They encode tumor-specific antigens recognized by autologous cytolytic T lymphocytes (CTLs). On the basis of semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) assays, 6 of the 12 members of the MAGE-A family, including MAGE-A1, were previously reported to have a high level of expression in tumors, whereas 5 other members, including MAGE-A10, were expressed at a much lower level, deemed to be insufficient for CTL recognition. However, analysis with antibodies has shown that some melanoma cell lines contain equivalent amounts of MAGE-A1 and MAGE-A10 proteins. This discrepancy appeared to be due to the low efficacy of the primers that had been used for the previous MAGE-A10 RT-PCR assays. This led us to develop a method that is independent of the efficacy of the PCR primers to evaluate MAGE-A gene expression. cDNA libraries from tumor cell lines were introduced into bacteria, of which 200 pools of about 500 bacteria were maintained in microcultures. The frequencies of the MAGE-A cDNA clones in each library were evaluated by performing PCR assays on each of these pools. The abundance of MAGE-A10 cDNAs was found to be similar to that of MAGE-A1 in 3 of the libraries that were analyzed, including 2 with high expression (1/6,400), confirming that MAGE-A10 is expressed at a high level. MAGE-A2, A3, A4, A6 and A12 cDNAs were also confirmed often to be present at a frequency of more than 1/10,000, a level of expression that should suffice for recognition of antigenic peptides encoded by these genes by cytolytic T cells. The remaining MAGE genes are either not expressed in tumors or are expressed at a very low level, with the exception of MAGE-A8 and 11, which show high expression in a very small number of tumors. This method also allowed us to isolate 5 MAGE-A cDNAs that we had not obtained previously, enabling us to delineate the exons in the sequences of genes MAGE-A5, A8, A9, A10 and A11.
Keywords
Antigens, Neoplasm/genetics, Antigens, Neoplasm/isolation & purification, Chromosome Mapping, Gene Expression Regulation, Neoplastic, Gene Library, Humans, Male, Melanoma-Specific Antigens, Neoplasm Proteins/genetics, Neoplasm Proteins/isolation & purification, Placenta/metabolism, RNA, Messenger/metabolism, Reverse Transcriptase Polymerase Chain Reaction, Testis/metabolism, Tumor Cells, Cultured
Pubmed
Web of science
Create date
19/11/2007 13:00
Last modification date
20/08/2019 13:37
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