Evaluation of INK4A promoter methylation using pyrosequencing and circulating cell-free DNA from patients with hepatocellular carcinoma
G Huang, JD Krocker, JL Kirk, SN Merwat… - Clinical Chemistry and …, 2014 - degruyter.com
G Huang, JD Krocker, JL Kirk, SN Merwat, H Ju, RD Soloway, LR Wieck, A Li…
Clinical Chemistry and Laboratory Medicine (CCLM), 2014•degruyter.comAbstract Background: Hyper-methylation of CpG dinucleotides in the promoter region of
inhibitor of cyclin-dependent kinase 4A (INK4A) has been reported in 60%–80% of
hepatocellular carcinoma (HCC). As INK4A promoter hypermethylation event occurs early in
HCC progression, the quantification of INK4A promoter methylation in blood sample may
represent a useful biomarker for non-invasive diagnosis and prediction of response to
therapy. Methods: We examined INK4A promoter methylation using circulating cell-free DNA …
inhibitor of cyclin-dependent kinase 4A (INK4A) has been reported in 60%–80% of
hepatocellular carcinoma (HCC). As INK4A promoter hypermethylation event occurs early in
HCC progression, the quantification of INK4A promoter methylation in blood sample may
represent a useful biomarker for non-invasive diagnosis and prediction of response to
therapy. Methods: We examined INK4A promoter methylation using circulating cell-free DNA …
Abstract
Background: Hyper-methylation of CpG dinucleotides in the promoter region of inhibitor of cyclin-dependent kinase 4A (INK4A) has been reported in 60%–80% of hepatocellular carcinoma (HCC). As INK4A promoter hypermethylation event occurs early in HCC progression, the quantification of INK4A promoter methylation in blood sample may represent a useful biomarker for non-invasive diagnosis and prediction of response to therapy.
Methods: We examined INK4A promoter methylation using circulating cell-free DNA (ccfDNA) in a total of 109 serum specimens, including 66 HCC and 43 benign chronic liver diseases. Methylation of the individual seven CpG sites was examined using pyrosequencing.
Results: Our results showed that there were significantly higher levels of methylated INK4A in HCC specimens than controls and that the seven CpG sites had different levels of methylation and might exist in different PCR amplicons. The area under receiver operating characteristic (ROC) curve was 0.82, with 65.3% sensitivity and 87.2% specificity at 5% (LOD), 39.0% sensitivity and 96.5% specificity at 7% LOD, and 20.3% sensitivity and 98.8% specificity at 10% LOD, respectively.
Conclusions: Our results support additional studies incorporating INK4A methylation testing of ccfDNA to further validate the diagnostic, predictive, and prognostic characteristics of this biomarker in HCC patients. The knowledge of the existence of epi-alleles should help improve assay design to maximize detection.
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