Article ID Journal Published Year Pages File Type
5527770 Leukemia Research 2017 6 Pages PDF
Abstract

•RASSF6 and RASSF10 were frequently hypermethylated at diagnosis in adult ALL.•RASSF6 frequently methylated B-ALL; whereas, RASSF10 in T-ALL.•First to report RASSF6 methylation at a high frequency in pre-B ALL patients.•Methylation of RASSF6 was significantly associated with inferior OS in pre-B ALL.•Hypermethylation of RASSF6 can serve as a useful prognosis biomarker in pre-B-ALL.

BackgroundThe Hypermethylation of Ras association domain family (RASSF) often plays a key role in malignant progression of solid tumors; however, their impact on the prognosis and survival of adult ALL patients remain elusive.MethodsThe frequency of the promoter methylation pattern of RASSF6 and RASSF10 were analyzed in the peripheral blood (PB) samples taken at the time of diagnosis of 45 ALL patients. The methylation-specific PCR (MSP) assay was used to detect the DNA methylation patterns.ResultsRASSF6 was frequently hypermethylated in patients diagnosed with pre-B-ALL (90.9%) and B-ALL (87.5%), followed by T-ALL (66.7%); whereas, RASSF10 methylation was more confined to T-ALL (80%) as compared to B-ALL (25%) and pre-B ALL (9.1%) patients. Moreover, hypermethylation of RASSF6 was significantly associated with a poor prognosis and shorter overall survival (OS) in patients with pre-B-ALL (log-rank test; P = 0.041).ConclusionRASSF6 and RASSF10 were frequently hypermethylated in the samples at the time of diagnosis of adult ALL patients. Our study represents the first report of methylation of RASSF6 at a high frequency in patients with pre-B ALL. Furthermore, hypermethylation of RASSF6 was significantly associated with inferior overall survival in pre-B ALL patients. It may suggest that the frequent epigenetic inactivation of RASSF6 plays an important role in the pathogenesis and progression of pre-B-ALL.

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