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CpG island methylation of tumor-related genes in three primary central nervous system lymphomas in immunocompetent patients
We have determined the promoter CpG island methylation status of O 6-methylguanine-DNA methyltransferase ( MGMT), glutathione-S-transferase P1 ( GSTP1) , death-associated protein kinase ( DAPK) , p14 ARF, thrombospondin-1 ( THBS1) , tissue inhibitor of metalloproteinase-3 gene ( TIMP-3) , p73, p16 I...
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Published in: | Cancer genetics and cytogenetics 2003-04, Vol.142 (1), p.21-24 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We have determined the promoter CpG island methylation status of O
6-methylguanine-DNA methyltransferase (
MGMT), glutathione-S-transferase P1 (
GSTP1)
, death-associated protein kinase (
DAPK)
, p14
ARF, thrombospondin-1 (
THBS1)
, tissue inhibitor of metalloproteinase-3 gene (
TIMP-3)
, p73, p16
INK4A,
RB1, and
TP53 genes in three primary central nervous system lymphomas (PCNSL). Five genes (
GSTP1, DAPK, TIMP-3, p16
INK4A, and
RB1) were hypermethylated in two samples, whereas
MGMT, THBS1, and
p73 were aberrantly methylated in only one sample. No case presented CpG island methylation for the
p14
ARF and
TP53 genes. These findings concur with previous data suggesting a frequent inactivation of
p16
INK4A and very limited involvement of
TP53 in PCNSL and also provide insights into the epigenetic molecular involvement of other tumor-related genes in this neoplasm. |
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ISSN: | 0165-4608 1873-4456 |
DOI: | 10.1016/S0165-4608(02)00799-9 |