학술논문

Hypermethylation of secreted frizzled-related proteins predicts poor prognosis in non-M3 acute myeloid leukemia
Document Type
Report
Source
OncoTargets and Therapy. Annual, 2017, Vol. 10, p3635, 10 p.
Subject
Cellular proteins -- Health aspects
Cellular signal transduction -- Genetic aspects -- Health aspects
Gene expression -- Health aspects
Acute myelocytic leukemia -- Genetic aspects -- Development and progression -- Care and treatment
Language
English
ISSN
1178-6930
Abstract
Objective: Secreted frizzled-related proteins (SFRPs) as Wnt signaling antagonists have been found to be dysregulated by promoter hypermethylation in several cancers including acute myeloid leukemia (AML). This study aimed to investigate the methylated status of SFRPs promoter region and its clinical relevance in Chinese non-M3 AML patients. Methods: SFRPs methylation in 139 primary non-M3 AML patients was determined using methylation-specific real-time quantitative polymerase chain reaction. Results: The frequency of aberrant methylation was as follows: 30.2% for SFRP1, 27.3% for SFRP2, 5.0% for SFRP4, and 1.4% for SFRP5. Hypermethylation of at least one SFRP gene occurred in 51.8% (72/139) of non-M3 AML patient samples, which was significantly higher compared to normal control (0/21) (P Conclusion: These findings suggested that hypermethylation of SFRP1/2 was a frequent event and silenced SFRP1/2 expression in AML. Moreover, hypermethylation of SFRPs promoter was an adverse risk factor for OS in Chinese non-M3 AML patients. Keywords: SFRPs, methylation, RQ-MSP, non-M3 AML, prognosis
Introduction Acute myeloid leukemia (AML), the most common type of leukemia in adults, is a group of heterogeneous malignant disorders characterized by clonal proliferation and differentiation arrest of myeloid progenitor [...]