Tzoanopoulos Dimitrios, Speletas Matthaios, Arvanitidis Konstantinos, Veiopoulou Christina, Kyriaki Sofia, Thyphronitis George, Sideras Paschalis, Kartalis Georgios, Ritis Konstantinos
First Division of Internal Medicine, Democritus University of Thrace, Regional Hospital of Alexandroupolis, Alexandroupolis, Greece.
Br J Haematol. 2002 Oct;119(1):46-53. doi: 10.1046/j.1365-2141.2002.03829.x.
Chronic myeloid leukaemia (CML) is a malignant clonal disorder of the haematopoietic stem cell. Treatment of CML patients with interferon alpha (IFN-alpha) has induced haematological and cytogenetic remission. Interferons transcriptionally activate target genes through the JAK-STAT and interferon regulated factors (IRFs) family pathways. Interferon regulated factor-1 (IRF-1) is a transcriptional activator of genes critical for cell growth, differentiation and apoptosis. The skipping of exons 2 or 2 and 3 of IRF-1 in patients with myelodysplastic syndromes and acute myelogenous leukaemia suggests that this factor may have a critical role in leukaemogenesis. The role of IRF-1 in CML is currently unknown. Therefore, mutational analysis of IRF-1 was performed and its expression pattern was also studied in CML patients. We studied IRF-1 in peripheral blood mononuclear cells of 21 patients in chronic phase CML. No point mutations were identified at the cDNA level. Surprisingly, fourfold reduction of full-length IRF-1 mRNA expression was established in 17/21 patients compared with normal individuals. Low expression of full-length IRF-1 was observed in conjunction with high levels of aberrantly spliced mRNAs, reported for the first time. In three patients who were also analysed during blastic transformation, further reduction of full-length IRF-1 mRNA was observed. These findings demonstrate that, in CML patients, IRF-1 can produce high levels of aberrant spliced mRNAs with subsequent reduction in the levels of full-length IRF-1 mRNA. This observation is consistent with the notion that exon skipping may constitute another mechanism of tumour suppressor gene inactivation in this disease.
慢性粒细胞白血病(CML)是一种造血干细胞的恶性克隆性疾病。用α干扰素(IFN-α)治疗CML患者可诱导血液学和细胞遗传学缓解。干扰素通过JAK-STAT和干扰素调节因子(IRF)家族途径转录激活靶基因。干扰素调节因子-1(IRF-1)是对细胞生长、分化和凋亡至关重要的基因的转录激活因子。骨髓增生异常综合征和急性髓性白血病患者中IRF-1的外显子2或外显子2和3的跳跃表明该因子可能在白血病发生中起关键作用。IRF-1在CML中的作用目前尚不清楚。因此,我们对IRF-1进行了突变分析,并研究了其在CML患者中的表达模式。我们研究了21例慢性期CML患者外周血单个核细胞中的IRF-1。在cDNA水平未发现点突变。令人惊讶的是,与正常个体相比,17/21例患者中全长IRF-1 mRNA表达降低了四倍。首次报道,在全长IRF-1低表达的同时观察到高水平的异常剪接mRNA。在3例也在急变期进行分析的患者中,观察到全长IRF-1 mRNA进一步降低。这些发现表明,在CML患者中,IRF-1可产生高水平的异常剪接mRNA,随后全长IRF-1 mRNA水平降低。这一观察结果与外显子跳跃可能构成该疾病中肿瘤抑制基因失活的另一种机制的观点一致。