Epigenetic analysis of childhood acute lymphoblastic leukemia
| Autor: | Farida Latif, Thomas L. Dunwell, Eamonn R. Maher, Mike Griffiths, Luke B. Hesson, Anna T. Brini, Raffaella Chiaramonte, Vladimir I. Kashuba, Daniel Catchpoole, Veronika I. Zabarovska, Eugene R. Zabarovsky, Tatiana V. Pavlova |
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| Rok vydání: | 2009 |
| Předmět: |
Cancer Research
Molecular Sequence Data Biology Epigenesis Genetic Cell Line Tumor Gene expression medicine Humans Epigenetics Gene Silencing Molecular Biology Childhood Acute Lymphoblastic Leukemia Gene Oligonucleotide Array Sequence Analysis Genetics Thyroid hormone receptor Base Sequence Gene Expression Regulation Leukemic Gene Expression Profiling Cancer Methylation DNA Methylation Precursor Cell Lymphoblastic Leukemia-Lymphoma medicine.disease Chromosome 3 Cancer research Chromosomes Human Pair 3 |
| Zdroj: | Epigenetics. 4(3) |
| ISSN: | 1559-2308 |
| Popis: | We used a chromosome 3 wide NotI microarray for identification of epigenetically inactivated genes in childhood acute lymphoblastic leukemia (ALL). Three novel genes demonstrated frequent methylation in childhood ALL. PPP2R3A (protein phosphatase 2, regulatory subunit B", alpha) was frequently methylated in T (69%) and B (82%)-ALL. Whilst FBLN2 (fibulin 2) and THRB (thyroid hormone receptor, beta) showed frequent methylation in B-ALL (58%; 56% respectively), but were less frequently methylated in T-ALL (17% for both genes). Recently it was demonstrated that BNC1 (Basonuclin 1) and MSX1 (msh homeobox 1) were frequently methylated across common epithelial cancers. In our series of childhood ALL BNC1 was frequently methylated in both T (77%) and B-ALL (79%), whilst MSX1 showed T-ALL (25%) specific methylation. The methylation of the above five genes was cancer specific and expression of the genes could be restored in methylated leukemia cell lines treated with 5-aza-2'-deoxycytidine. This is the first report demonstrating frequent epigenetic inactivation of PPP2R3A, FBLN2, THRB, BNC1 and MSX1 in leukemia. The identification of frequently methylated genes showing cancer specific methylation will be useful in developing early cancer detection screens and for targeted epigenetic therapies. |
| Databáze: | OpenAIRE |
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