Distinct patterns of global promoter methylation in early stage chronic lymphocytic leukemia. Issue 3 (18th December 2013)
- Record Type:
- Journal Article
- Title:
- Distinct patterns of global promoter methylation in early stage chronic lymphocytic leukemia. Issue 3 (18th December 2013)
- Main Title:
- Distinct patterns of global promoter methylation in early stage chronic lymphocytic leukemia
- Authors:
- Ronchetti, Domenica
Tuana, Giacomo
Rinaldi, Andrea
Agnelli, Luca
Cutrona, Giovanna
Mosca, Laura
Fabris, Sonia
Matis, Serena
Colombo, Monica
Gentile, Massimo
Recchia, Anna Grazia
Kwee, Ivo
Bertoni, Francesco
Morabito, Fortunato
Ferrarini, Manlio
Neri, Antonino - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Genomic and epigenomic studies of chronic lymphocytic leukemia (CLL) are reshaping our understanding of the disease and have provided new perspectives for a more individualized diagnosis and new potential therapeutic targets. In this study, the global promoter methylation profile was determined in highly purified B‐cells from 37 (Binet stage A) CLL patients, using high‐resolution methylation microarrays (27, 578 CpG). Overall, the methylation pattern correlated with the major biological (ZAP‐70 and CD38), and molecular (<italic>IGHV</italic> mutation) markers, distinguishing CLL cases according to <italic>IGHV</italic> mutational status. Cell adhesion molecules were enriched in the signature of unmutated (UM) versus mutated (M‐) CLL. Moreover, in M‐CLL CpG hyper‐methylation in three genes, including <italic>SPG20</italic>, was significantly anti‐correlated with the corresponding gene expression level. Finally, the correlation between the methylation pattern and clinical parameters was investigated. Notably, out of 42 methyl‐probes that were significantly associated with progression free survival (PFS), hyper‐methylation of <italic>SPG20</italic> was also positively associated with PFS. These data support the notion that epigenetic changes have clinical impact in CLL and may contribute to the identification of novel candidate disease‐associated genes potentially useful to predict the<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Genomic and epigenomic studies of chronic lymphocytic leukemia (CLL) are reshaping our understanding of the disease and have provided new perspectives for a more individualized diagnosis and new potential therapeutic targets. In this study, the global promoter methylation profile was determined in highly purified B‐cells from 37 (Binet stage A) CLL patients, using high‐resolution methylation microarrays (27, 578 CpG). Overall, the methylation pattern correlated with the major biological (ZAP‐70 and CD38), and molecular (<italic>IGHV</italic> mutation) markers, distinguishing CLL cases according to <italic>IGHV</italic> mutational status. Cell adhesion molecules were enriched in the signature of unmutated (UM) versus mutated (M‐) CLL. Moreover, in M‐CLL CpG hyper‐methylation in three genes, including <italic>SPG20</italic>, was significantly anti‐correlated with the corresponding gene expression level. Finally, the correlation between the methylation pattern and clinical parameters was investigated. Notably, out of 42 methyl‐probes that were significantly associated with progression free survival (PFS), hyper‐methylation of <italic>SPG20</italic> was also positively associated with PFS. These data support the notion that epigenetic changes have clinical impact in CLL and may contribute to the identification of novel candidate disease‐associated genes potentially useful to predict the clinical outcome of early stage CLL patients. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Genes, chromosomes & cancer. Volume 53:Issue 3(2014:Mar.)
- Journal:
- Genes, chromosomes & cancer
- Issue:
- Volume 53:Issue 3(2014:Mar.)
- Issue Display:
- Volume 53, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 53
- Issue:
- 3
- Issue Sort Value:
- 2014-0053-0003-0000
- Page Start:
- 264
- Page End:
- 273
- Publication Date:
- 2013-12-18
- Subjects:
- Cancer -- Genetic aspects -- Periodicals
616.994042 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2264 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/gcc.22139 ↗
- Languages:
- English
- ISSNs:
- 1045-2257
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4111.763000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3082.xml