Sauerbrey A, Stammler G, Zintl F, Volm M
Department of Paediatrics, University of Jena, Germany.
Br J Haematol. 1996 Jul;94(1):99-104. doi: 10.1046/j.1365-2141.1996.d01-1753.x.
In a retrospective analysis, acute lymphoblastic leukaemia (ALL) blast cells of 102 children were investigated for the expression of the retinoblastoma susceptibility (RB)-1 gene at mRNA level by dot blot hybridization and semiquantitative RT-PCR. 56 patients were analysed by dot blot hybridization and 35 representative patients out of this group by semiquantitative RT-PCR. Two additional groups of patients (23 patients with initial and 23 patients with relapsed ALL) were also investigated by semiquantitative RT-PCR. RB-1 gene expression was detectable in all investigated ALL at different levels. According to the relative mRNA expression the patients were discriminated by the median value in groups with low or high RB-1 expression. The Kaplan-Meier estimates showed that patients with low RB-1 expression had a lower probability of remaining in first remission (P = 0.03) and a significantly higher risk to succumb to their disease (P = 0.03). Furthermore, the comparison of the results between initial and relapsed ALL showed that the relapses had significantly lower RB-1 mRNA expression (P = 0.02). The overall survival of the patients was shorter in both groups when RB-1 gene expression was low. A multivariate analysis, including age, sex, immunological subtype, initial white blood cell count and RB-1 expression, identified RB-1 as an independent prognostic predictor (P = 0.017) in addition to the initial white blood cell count (P = 0.00001). In conclusion, low RB-1 expression is an unfavourable prognostic predictor in initial and relapsed childhood ALL. The RB-1 gene expression in relapsed ALL is significantly lower than in initial ALL.
在一项回顾性分析中,通过斑点杂交和半定量逆转录聚合酶链反应(RT-PCR),在mRNA水平上研究了102例儿童急性淋巴细胞白血病(ALL)原始细胞中视网膜母细胞瘤易感(RB)-1基因的表达。56例患者通过斑点杂交进行分析,该组中的35例代表性患者通过半定量RT-PCR进行分析。另外两组患者(23例初发ALL患者和23例复发ALL患者)也通过半定量RT-PCR进行了研究。在所有研究的ALL中均能检测到不同水平的RB-1基因表达。根据相对mRNA表达,通过RB-1低表达或高表达组的中值对患者进行区分。Kaplan-Meier估计显示,RB-1低表达的患者首次缓解的概率较低(P = 0.03),死于疾病的风险显著更高(P = 0.03)。此外,初发ALL和复发ALL结果的比较表明,复发患者的RB-1 mRNA表达显著更低(P = 0.02)。当RB-1基因表达低时,两组患者的总生存期均较短。多因素分析包括年龄、性别、免疫亚型、初发白细胞计数和RB-1表达,确定RB-1除了初发白细胞计数(P = 0.00001)外,还是一个独立的预后预测指标(P = 0.017)。总之,RB-1低表达是儿童初发和复发ALL的不良预后预测指标。复发ALL中的RB-1基因表达显著低于初发ALL。