Tsukamoto Norifumi, Karasawa Masamitsu, Tanaka Yoko, Yokohama Akihiko, Uchiumi Hideki, Matsushima Takafumi, Murakami Hirokazu, Nojima Yoshihisa
Third Department of Internal Medicine, Gunma University School of Medicine, Maebashi, Gunma, Japan.
Int J Hematol. 2003 Nov;78(4):362-9. doi: 10.1007/BF02983563.
The AML1/ETO fusion gene is expressed in virtually all patients with t(8;21)(q22;q22) acute myelogenous leukemia (AML). Long-term complete remission (CR) of AML with t(8;21) has been observed despite the presence of residual AML1/ ETO fusion transcripts, although detection may depend on the sensitivity of the methods used. We examined a patient with recurrent AML who showed the t(8;21)(q22;q22) chromosomal abnormality following a CR of 15 years. The blast cells at the time of recurrence expressed the AML1/ETO fusion transcript, and the breakpoint of the AML1 gene was located on intron 5. Southern blot analysis of the DNA extracted from bone marrow slides that had been made and stored for 15 years revealed the same rearrangement pattern of the AML1 gene. Furthermore, the junction sequences between the AML1 and the ETO genes, analyzed by long-distance inverse polymerase chain reaction, proved to be completely identical. These findings can be interpreted in two ways: (1) The initial leukemia clone persisted and finally relapsed after 15 years in the dormant state. (2) AML developed in different subclones having the same AML1/ETO junctional sequences but with additional genetic changes (second hit).
AML1/ETO融合基因在几乎所有t(8;21)(q22;q22)急性髓性白血病(AML)患者中均有表达。尽管存在残留的AML1/ETO融合转录本,但t(8;21) AML患者仍可实现长期完全缓解(CR),不过检测可能取决于所用方法的敏感性。我们研究了一名复发性AML患者,该患者在15年的CR后出现了t(8;21)(q22;q22)染色体异常。复发时的原始细胞表达AML1/ETO融合转录本,且AML1基因的断点位于第5内含子。对15年前制作并保存的骨髓玻片提取的DNA进行Southern印迹分析,结果显示AML1基因的重排模式相同。此外,通过长距离反向聚合酶链反应分析的AML1和ETO基因之间的连接序列完全相同。这些发现可以有两种解释:(1)初始白血病克隆持续存在,最终在休眠状态下15年后复发。(2)AML在具有相同AML1/ETO连接序列但有额外基因改变(二次打击)的不同亚克隆中发生。