Siehl Jan M, Reinwald Mark, Heufelder Karin, Menssen Hans D, Keilholz Ulrich, Thiel Eckhard
Med. Klinik III (Hematology, Oncology and Transfusion Medicine), Charité Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12200 Berlin, Germany.
Ann Hematol. 2004 Dec;83(12):745-50. doi: 10.1007/s00277-004-0941-0. Epub 2004 Aug 31.
WT1 is a transcription factor involved in differentiation and proliferation of acute myeloid leukemia (AML) blasts and is expressed in 90% of cases, as determined by nested reverse transcription polymerase chain reaction (RT-PCR). It is proposed to be a key molecule in leukemia promotion. To assess the relevance of WT1 expression, we analyzed blood and bone marrow samples from 58 AML patients (37 at diagnosis, 8 in hematological remission, and 13 at relapse) for the level of WT1 expression, using quantitative real-time RT-PCR. In addition, 21 randomly chosen samples were also analyzed for the quantitative expression of the main WT1 splice variants. As expected, samples from patients at the time of diagnosis or relapse showed significantly higher WT1 expression compared to samples from patients in remission or control samples. No striking difference in expression levels was found between various French-American-British (FAB) subtypes. The level of WT1 expression observed in patients at the time of initial diagnosis was similarly high in patients at relapse. Expression of the four main isoforms (E5+/KTS+, E5-/KTS+, E5+/KTS-, and E5-/KTS-) was found in all samples with significantly higher expression levels of the E5+ variants. Together, these findings support the potential of WT1 as a target for novel treatment approaches in AML.
WT1是一种转录因子,参与急性髓系白血病(AML)原始细胞的分化和增殖,通过巢式逆转录聚合酶链反应(RT-PCR)测定,90%的病例中可检测到其表达。它被认为是白血病进展中的关键分子。为了评估WT1表达的相关性,我们使用定量实时RT-PCR分析了58例AML患者(37例诊断时、8例血液学缓解期和13例复发期)的血液和骨髓样本中WT1的表达水平。此外,还对21个随机选择的样本进行了主要WT1剪接变体的定量表达分析。正如预期的那样,与缓解期患者的样本或对照样本相比,诊断时或复发时患者的样本显示出显著更高的WT1表达。在不同的法美英(FAB)亚型之间未发现表达水平的显著差异。初诊时患者中观察到的WT1表达水平在复发患者中同样很高。在所有样本中均发现了四种主要异构体(E5+/KTS+、E5-/KTS+、E5+/KTS-和E5-/KTS-)的表达,其中E5+变体的表达水平显著更高。这些发现共同支持了WT1作为AML新型治疗方法靶点的潜力。