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Correlation of postoperative recurrence in hepatocellular carcinoma with demethylation of repetitive sequences
- Source :
- Oncogene. 21(5)
- Publication Year :
- 2001
-
Abstract
- Restriction landmark genomic scanning (RLGS) was utilized to identify novel genomic alterations in hepatocellular carcinoma (HCC). Thirty-one HCC samples were examined by RLGS. Two high intensity spots were common to several RLGS profiles of different HCCs. Nucleotide sequencing and homology search analysis showed that these spots represented repetitive sequences, Human tandem repeat sequence (Genbank, L09552) and centromeric NotI cluster (Genbank, Y10752). These intensified signals were attributable to the occurrence of demethylated areas in the recognition sequence of the NotI site of the corresponding fragments. The intensity of these spots in the RLGS profile reflects their degree of demethylation, which was significantly correlated with postoperative recurrence, even in patients regarded as belonging to the good prognosis group by conventional prognostic factors. Multivariate analysis showed that the intensities of the two spots retained independent prognostic value. This is a new type of predictive factor for HCC based on epigenetic changes in hepatocarcinogenesis, and in the future it is expected to be of great value in making preoperative diagnosis and selecting postoperative therapy.
- Subjects :
- Adult
Male
Cancer Research
Carcinoma, Hepatocellular
Restriction landmark genomic scanning
Molecular Sequence Data
Restriction Mapping
Biology
medicine.disease_cause
Homology (biology)
Disease-Free Survival
Recognition sequence
Genetics
medicine
Humans
Epigenetics
Postoperative Period
Repeated sequence
Molecular Biology
Aged
Liver Neoplasms
Sequence Analysis, DNA
DNA Methylation
Middle Aged
medicine.disease
Prognosis
Treatment Outcome
Liver
Tandem Repeat Sequences
Hepatocellular carcinoma
GenBank
Cancer research
Female
Neoplasm Recurrence, Local
Carcinogenesis
Subjects
Details
- ISSN :
- 09509232
- Volume :
- 21
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Oncogene
- Accession number :
- edsair.doi.dedup.....4c3266a9813c410f73f301017ca16008