Methylation status of CpG islands in secreted frizzled-related protein gene promoter region of malignant hematopoietic cell lines.
- Author:
Cheng-Bo XU
1
,
2
;
Jian-Zhen SHEN
;
Song-Fei SHEN
;
Hai-Ying FU
;
Xue-Mei WU
;
Dan-Sen WU
;
Yi-Fang ZHU
;
Lu CHEN
Author Information
1. Department of Hematology, Union Hospital, Fujian Medical University
2. Fujian Institute of Hematology, Fuzhou 350001, Fujian Province, China.
- Publication Type:Journal Article
- MeSH:
Cell Line, Tumor;
CpG Islands;
DNA Methylation;
Hematologic Neoplasms;
genetics;
Humans;
Intercellular Signaling Peptides and Proteins;
genetics;
Membrane Proteins;
genetics;
Promoter Regions, Genetic;
Proto-Oncogene Proteins;
genetics
- From:
Journal of Experimental Hematology
2009;17(6):1487-1491
- CountryChina
- Language:Chinese
-
Abstract:
To investigate the methylation status of CpG islands of the secreted frizzled-related protein (SFRP) gene promoter region in malignant hematopoietic cell lines, and to explore the possible relationship of CpG abnormal methylation status with pathogenic mechanism of hematologic malignancies. Methylation-specific PCR was used to detect the status of SFRP gene promoter region in nine malignant hematopoietic cell lines and peripheral blood mononuclear cells from healthy people. The results indicated that hypermethylation of 2 genes coding for SFRP1 and 2 were present in nine malignant hematopoietic cell lines, however, methylation and unmethylation of SFRP4 were both detected in CA46, HL60 and U937 cell lines, and SFRP5 in U266 as well. None of the normal mononuclear cells showed methylation of SFRP 1-5 genes. It is concluded that the hypermethylation of SFRP genes is related to the evolution of malignant hematopoiesis. Methylation of SFRP genes may serve as potential independent biomarkers for early detection of hematologic malignancies.