Methods for detecting epigenetic modifications
View Patent ↗A method of detecting a predisposition to, or the incidence of, cancer in a sample comprises detecting an epigenetic change in at least one gene selected from an NDRG4/NDRG2 subfamily gene, GATA4, OSMR, GATA5, SFRP1, ADAM23, JPH3, SFRP2, APC, MGMT, TFPI2, BNIP3, FOXE1, SYNE1, S0X17, PHACTR3 and JAM3, wherein detection of the epigenetic change is indicative of a predisposition to, or the incidence of, cancer. Also described are pharmacogenetic methods for determining suitable treatment regimens for cancer and methods for treating cancer patients, based around selection of the patients according to the methods of the invention. The present invention is also concerned with improved methods of collecting, processing and analyzing samples, in particular body fluid samples. These methods may be useful in diagnosing, staging or otherwise characterizing various diseases. The invention also relates to methods for identifying, diagnosing, staging or otherwise characterizing cancers, in particular gastrointestinal cancers such as colorectal cancers, gastric cancers and oesophageal cancers. The methods of the invention relate, inter alia, to isolating and analyzing the human DNA component from faecal samples and blood-based samples.
1. A method of detecting a predisposition to, or the incidence of, colorectal cancer in a sample taken from a human, the sample comprising genomic DNA from colorectal cells, the method comprising:
(a) creating modified genomic DNA by treating the genomic DNA from colorectal cells from the sample with a reagent which selectively modifies unmethylated cytosine residues in the DNA contained in the sample to produce detectable modified residues but which does not modify methylated cytosine residues;
(b) determining the methylation status of the promoter region of the NDRG4 gene comprising the nucleotide sequence of SEQ ID NO: 524, comprising hybridizing to the promoter region of the NDRG4 gene comprising the nucleotide sequence of SEQ ID NO: 524 a primer and/or probe that specifically hybridizes to the treated genomic DNA depending on its methylation status; and
(c) detecting hypermethylation of the promoter region of the NDRG4 gene comprising the nucleotide sequence of SEQ ID NO: 524, and correlating the detected hypermethylation with a predisposition to, or the incidence of, colorectal cancer in said sample taken from a human.
2. The method of claim which comprises determining methylation status in a panel of genes comprising NDRG4 and at least one gene selected from the group consisting of GATA4, OSMR, GATA5, SFRP1, ADAM23, JPH3, SFRP2, APC, MGMT, TFPI2, BNIP3, FOXE1, SYNE1, SOX17, PHACTR3 and JAM3.
3. The method of claim 1 wherein the sample comprises a tissue sample or a bodily fluid sample.
4. The method of claim 3 wherein the bodily fluid sample comprises a faecal sample.
5. The method of claim 3 wherein the tissue sample comprises a colon or rectal or appendix sample.
6. The method of claim 3 wherein the bodily fluid sample comprises a blood sample or a derivative thereof.
7. The method according to claim 1 where said primer and/or probe is selected from primers comprising SEQ ID NO: 7-10, 13-18, 58, 59, 62, 63, 65, 67, 69, 70, 72, 73, 75, 76, 78, 80, 81, 83, 84, 86, 89, 92, 93 or 570, and probes comprising SEQ ID NO: 19, 57, 60, 61, 64, 66, 68, 71, 74, 77, 79, 82, 85, 87, 88, 91 or 94.
8. The method of claim 1 wherein the reagent is a bisulfite reagent.