Figure 1
Figure 1. Methylation of SFRP promoters in AML cell lines and childhood patients with AML. (A) MSP (top) and real-time RT-PCR (bottom) analysis of SFRP promoter methylation and expression in 6 AML cell lines. M and U represent PCR products with primers specific for the methylated and unmethylated sequences, respectively. SFRP mRNA levels were normalized to GAPDH and compared with the mean expression levels of 3 normal BM samples. Results are presented as mean ± SE from triplicate assays. Note that SFRP promoter methylation was associated with mRNA down-regulation in these cell lines. (B) Semiquantitative RT-PCR analysis of SFRP expression in MV4-11 cells after treatment with the DNA demethylating agent 5′-AZA. Amplification of GAPDH cDNA served as internal control. (C) Representative MSP analysis of the 4 SFRP promoters in 5 childhood patients with AML (AML-1 to -5). The results of positive (LP1 and HeLa cell lines) and negative (NPB, normal peripheral blood) controls are also shown.

Methylation of SFRP promoters in AML cell lines and childhood patients with AML. (A) MSP (top) and real-time RT-PCR (bottom) analysis of SFRP promoter methylation and expression in 6 AML cell lines. M and U represent PCR products with primers specific for the methylated and unmethylated sequences, respectively. SFRP mRNA levels were normalized to GAPDH and compared with the mean expression levels of 3 normal BM samples. Results are presented as mean ± SE from triplicate assays. Note that SFRP promoter methylation was associated with mRNA down-regulation in these cell lines. (B) Semiquantitative RT-PCR analysis of SFRP expression in MV4-11 cells after treatment with the DNA demethylating agent 5′-AZA. Amplification of GAPDH cDNA served as internal control. (C) Representative MSP analysis of the 4 SFRP promoters in 5 childhood patients with AML (AML-1 to -5). The results of positive (LP1 and HeLa cell lines) and negative (NPB, normal peripheral blood) controls are also shown.

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