Title: Abnormal methylation of the common PARK2 and PACRG promoter is associated with downregulation of gene expression in acute lymphoblastic leukemia and chronic myeloid leukemia
Authors: Agirre, Xabier ×
Román-Gómez, José
Vázquez, Iria
Jiménez-Velasco, Antonio
Garate, Leire
Montiel-Duarte, Cristina
Artieda, Paula
Cordeu, Lucia
Lahortiga, Idoya
Calasanz, María José
Heiniger, Anabel
Torres, Antonio
Minna, John D
Prósper, Felipe #
Issue Date: Feb-2006
Series Title: International Journal of Cancer vol:118 issue:8 pages:1945-53
Abstract: The PARK2 gene, previously identified as a mutated target in patients with autosomal recessive juvenile parkinsonism (ARJP), has recently been found to be a candidate tumor suppressor gene in ovarian, breast, lung and hepatocellular carcinoma that maps to the third common fragile site (CFS) FRA6E. PARK2 is linked to a novel described PACRG gene by a bidirectional promoter containing a defined CpG island in its common promoter region. We have studied the role of promoter hypermethylation in the regulation of PARK2 and PACRG expression in different tumor cell lines and primary patient samples. Abnormal methylation of the common promoter of PARK2 and PACRG was observed in 26% of patients with acute lymphoblastic leukemia and 20% of patients with chronic myelogenous leukemia (CML) in lymphoid blast crisis, but not in ovarian, breast, lung, neuroblastoma, astrocytoma or colon cancer cells. Abnormal methylation resulted in downregulation of PARK2 and PACRG gene expression, while demethylation of ALL cells resulted in demethylation of the promoter and upregulation of PARK2 and PACRG expression. By FISH, we demonstrated that a lack of PARK2 and PACRG expression was due to biallelic hypermethylation and not to deletion of either PARK2 or PACRG in ALL. In conclusion, our results demonstrate for the first time that the candidate tumor suppressor genes PARK2 and PACRG are epigenetically regulated in human leukemia, suggesting that abnormal methylation and regulation of PARK2 and PACRG may play a role in the pathogenesis and development of this hematological neoplasm.
ISSN: 0020-7136
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Molecular Genetics Section (-)
× corresponding author
# (joint) last author

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