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Epigenetic changes in multiple genes are emerging as an important mechanism for tumour cells to acquire resistance to chemotherapy. In the present work, we test the hypothesis that epigenetic organisation in cancer cells can be affected by cytostatic drugs. Colorectal cancer cells were cultured for several weeks in the presence of 6-thioguanine. Bisulphite sequencing of the CpG-rich promoter regions of two expressed genes showed a significantly increased frequency of methylated CpG sites in drug-treated cells, as compared with controls: 4.7% and 1.7%, respectively, for the HPRT gene; and 11.1% and 8.2% for CDX1. Essentially, all of the increase for the CDX1 gene was in a four CpG sub-region previously found to correlate with gene activity (P=0.006). This pattern of sparse promoter methylation fits with a recently proposed 'seeding' two-step mechanism leading up to gene inactivation in cancer cells. Taken together, our findings suggest activation in cancer cells of an epigenetic process enabling a tumour to generate drug-resistant variant cells.

Original publication




Journal article


Eur J Cancer

Publication Date





947 - 954


Antimetabolites, Antineoplastic, Colorectal Neoplasms, DNA Methylation, Drug Resistance, Neoplasm, Epigenesis, Genetic, Homeodomain Proteins, Humans, Hypoxanthine Phosphoribosyltransferase, Lymphocytes, Promoter Regions, Genetic, Sulfites, Thioguanine, Tumor Cells, Cultured