Possible regulation of Wilms’ tumour gene 1 (WT1) expression by the paired box genes PAX2 and PAX8 and by the haematopoietic transcription factor GATA‐1 in human acute myeloid leukaemias

生物 造血 转录因子 旅客8 威尔姆斯瘤 癌症研究 髓样 下调和上调 骨髓 关贸总协定 逆转录聚合酶链式反应 基因 基因表达 实时聚合酶链反应 干细胞 免疫学 遗传学
作者
Jan Siehl,Eckhard Thiel,Karin Heufelder,Emilian Snarski,Stefan Schwartz,Volker Mailänder,Ulrich Keilholz
出处
期刊:British Journal of Haematology [Wiley]
卷期号:123 (2): 235-242 被引量:32
标识
DOI:10.1046/j.1365-2141.2003.04622.x
摘要

Summary. Overexpression of the embryonic transcription factor, Wilms’ tumour protein 1 (WT1), is common in acute myeloid leukaemias (AML). Mutations of Wilms’ tumour gene 1 ( WT1 ) in AML are rare and WT1 expression may be increased by other transcription factors. PAX2 , PAX8 and GATA‐1 are known physiological regulators of WT1 . In the present study, we analysed either bone marrow or blood samples of 43 AML patients for the expression levels of WT1 , PAX2 , PAX8 and GATA‐1 by real‐time reverse transcription polymerase chain reaction (LightCycler). Bone marrow samples of patients without haematological malignancies and stem cell preparation samples from healthy donors and lymphoma patients served as controls. PAX2 expression was found in 11 of 43 AML samples, with a clear correlation of PAX2 with WT1 expression levels observed. PAX8 expression was found in two additional samples. GATA‐1 expression was detectable in 41 of 43 AML samples and also in all control samples; no significant differences between these groups were observed and no correlation of GATA‐1 expression with WT1 expression levels was apparent. In conclusion, PAX2 , and possibly PAX8 , appears to be a candidate for the upregulation of WT1 in a proportion of AML, whereas GATA‐1 expression cannot be explained as an inducer of WT1 . In two‐thirds of leukaemias from our series, the basis of WT1 upregulation cannot be explained by the simple upregulation of the known WT1 activators.
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