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Differential Methylation Pattern of ID4, SFRP1, and SHP1 between Acute Myeloid Leukemia and Chronic Myeloid Leukemia
- Authors
- Uhm, Kyung-Ok; Lee, Eun Soo; Lee, Yun Mi; Park, Jeong Seon; Kim, Seok Jin; Kim, Byung Soo; Kim, Hyeon Soo; Park, Sun-Hwa
- Issue Date
- Jun-2009
- Publisher
- KOREAN ACAD MEDICAL SCIENCES
- Keywords
- Leukemia, Myeloid, Acute; Chronic, BCR-ABL Positive; DNA Methylation
- Citation
- JOURNAL OF KOREAN MEDICAL SCIENCE, v.24, no.3, pp 493 - 497
- Pages
- 5
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- JOURNAL OF KOREAN MEDICAL SCIENCE
- Volume
- 24
- Number
- 3
- Start Page
- 493
- End Page
- 497
- ISSN
- 1011-8934
1598-6357
- Abstract
- To gain insight into the differential mechanism of gene promoter hypermethylation in acute and chronic leukemia, we identified the methylation status on one part of 5'CpG rich region of 8 genes, DAB2IP, DLC-1, H-cadherin, 04, Integrin alpha 4, RUNX3, SFRP1, and SHP1 in bone marrows from acute myeloid leukemia (AML) and chronic myeloid leukemia (CIVIL) patients. Also, we compared the methylation status of genes in AML and CML using methylation-specific PCR (MSP). The frequencies of DNA methylation of ID4, SFRP1, and SHP1 were higher in AML patients compared to those in CIVIL patients. In contrast, no statistical difference between AML and CIVIL was detected for other genes such as DLC-1, DAB2IP, H-Cadherin, Integrin,74, and RUNX3. Taken together, these results suggest that these methylation-control led genes may have different roles in AML and CIVIL, and thus, may act as a biological marker of AML.
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Related Researcher
- Kim, Hyeon Soo
- College of Medicine (Department of Anatomy)