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As a typical tumor suppressor gene, transcriptional silencing of ras-association domain family 1, isoform A (
RASSF1A
) is caused by biallelic methylation or the condition that one allele is methylated and then the other allele lost by allelic loss, as second hit.
RASSF1A
is inactivated epigenetically and thus down-regulated in many solid tumors. In summary, for the first time, we analyzed the expression status of
RASSF1A
in a cohort of 56
de novo
acute myeloid leukemia (AML) patients using quantitative real-time polymerase chain reaction. Results of our study indicate that patients with AML exhibited no differences in the
RASSF1A
gene expression comparing to normal controls. In conclusion, expression status of
RASSF1A
remained intact in our target samples, indicating that
RASSF1A
expression variation does not participate in the pathogenesis and the progression of AML.