Hypermethylation of Wnt antagonist gene promoters and activation of Wnt pathway in myelodysplastic marrow cells

被引：19

作者：

Masala, Erico ^{[1
]}

Valencia, Ana ^{[1
]}

Buchi, Francesca ^{[1
]}

Nosi, Daniele ^{[2
]}

Spinelli, Elena ^{[1
]}

Gozzini, Antonella ^{[1
]}

Sassolini, Francesca ^{[1
]}

Sanna, Alessandro ^{[1
]}

Zecchi, Sandra ^{[2
]}

Bosi, Alberto ^{[1
]}

Santini, Valeria ^{[1
]}

机构：

[1] Univ Florence, Funct Unit Haematol, AOU Careggi, I-50134 Florence, Italy

[2] Univ Florence, Dept Human Anat, I-50134 Florence, Italy

来源：

LEUKEMIA RESEARCH | 2012年 / 36卷 / 10期

关键词：

MDS; Methylation; Wnt pathway; Wnt antagonists; beta-Catenin; Azacitidine; ACUTE MYELOID-LEUKEMIA; SIGNALING PATHWAY; METHYLATION; MDS;

D O I：

10.1016/j.leukres.2012.05.023

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

We observed aberrant gene methylation of Wnt antagonists: sFRP1, sFRP2, sFRP4, sFRP5 and DKK1 in marrow cells of 55 MDS cases. Methylation of Wnt antagonist genes was associated with activation of the Wnt signaling pathway, consistent with the up-regulation of the Wnt downstream genes TCF1 and LEF1. Azacitidine exposure induced demethylation of Wnt-antagonist gene promoters and reduction of the non-phosphorylated beta-catenin (NPBC) which is prevalent during Wnt pathway inactivation. Presence of >= 5% of bone marrow blasts was associated with methylation of sFRP1 and DKK1 and with methylation of more than two of the five Wnt antagonist genes. (C) 2012 Elsevier Ltd. All rights reserved.

引用

页码：1290 / 1295

页数：6

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