Hernández A, Hernández P, Corral L, Muñiz A, Alaez C, Espinosa E, Fernández O, Martinez G
Instituto de Hematologia e Inmunologia, Cuidad de La Habana, Cuba.
Ann Hematol. 1993 Feb;66(2):81-3. doi: 10.1007/BF01695889.
We performed Southern-blot analysis of the p53 gene in 41 consecutive patients with typical chronic myelocytic leukemia (CML). In two of them, we were able to study cells during both the chronic and the accelerated phases. Only one of the 29 chronic-phase samples had rearrangement of the p53 gene, whereas three of the nine accelerated-phase samples and one of the five patients in blast crisis exhibited rearrangements. Gene deletion was observed in two patients, one in accelerated phase and the other in blast crisis. One patient with a nonrearranged p53 gene in chronic phase showed rearrangement after progression to the accelerated phase. On the other hand, one patient in accelerated phase exhibited rearrangements which disappeared after reversion to chronic phase with successful treatment. Our findings support the opinion that alterations of the p53 gene may play an important role in CML evolution.
我们对41例连续性典型慢性粒细胞白血病(CML)患者的p53基因进行了Southern印迹分析。其中2例患者,我们能够在慢性期和加速期均对细胞进行研究。29例慢性期样本中只有1例p53基因发生重排,而9例加速期样本中有3例以及5例急变期患者中有1例出现重排。在2例患者中观察到基因缺失,1例处于加速期,另1例处于急变期。1例慢性期p53基因未重排的患者在病情进展至加速期后出现重排。另一方面,1例加速期患者出现的重排在成功治疗后病情逆转至慢性期时消失。我们的研究结果支持以下观点,即p53基因改变可能在CML演变中起重要作用。