Epigenetic silencing of AXIN2 in colorectal carcinoma with microsatellite instability
pmid: 16247484
Epigenetic silencing of AXIN2 in colorectal carcinoma with microsatellite instability
Mutation or epigenetic silencing of mismatch repair genes, such as MLH1 and MSH2, results in microsatellite instability (MSI) in the genome of a subset of colorectal carcinomas (CRCs). However, little is yet known of genes that directly contribute to tumor formation in such cancers. To characterize MSI-dependent changes in gene expression, we have now compared transcriptomes between fresh CRC specimens positive or negative for MSI (n=10 for each) with the use of high-density oligonucleotide microarrays harboring >44,000 probe sets. Correspondence analysis of the expression patterns of isolated MSI-associated genes revealed that the transcriptome of MSI+ CRCs is clearly distinct from that of MSI- CRCs. Such MSI-associated genes included that for AXIN2, an important component of the WNT signaling pathway. AXIN2 was silenced, apparently as a result of extensive methylation of its promoter region, specifically in MSI+ CRC specimens. Forced expression of AXIN2, either by treatment with 5'-azacytidine or by transfection with AXIN2 cDNA, resulted in rapid cell death in an MSI+ CRC cell line. These data indicate that epigenetic silencing of AXIN2 is specifically associated with carcinogenesis in MSI+ CRCs.
- Mayo Clinic United States
- Japan Science and Technology Agency Japan
Adult, Aged, 80 and over, DNA, Complementary, Cell Death, DNA Repair, DNA Methylation, Diamines, Epigenesis, Genetic, Cytoskeletal Proteins, Axin Protein, Cell Line, Tumor, Azacitidine, Cluster Analysis, CpG Islands, Benzothiazoles, Carrier Proteins, Colorectal Neoplasms, Adaptor Proteins, Signal Transducing, Aged, Cell Proliferation
Adult, Aged, 80 and over, DNA, Complementary, Cell Death, DNA Repair, DNA Methylation, Diamines, Epigenesis, Genetic, Cytoskeletal Proteins, Axin Protein, Cell Line, Tumor, Azacitidine, Cluster Analysis, CpG Islands, Benzothiazoles, Carrier Proteins, Colorectal Neoplasms, Adaptor Proteins, Signal Transducing, Aged, Cell Proliferation
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