Xue Y Q
Jiangsu Institute of Hematology, Suzhou.
Zhonghua Yi Xue Za Zhi. 1993 Apr;73(4):209-12, 252-3.
Cytogenetic and molecular studies were made in 4 patients with Ph negative chronic myelogenous leukemia (CML) and 4 patients with CML with unusual Ph translocation. Chromosome analysis was performed on direct preparations and short-term cultures of bone marrow cells by R and G bandings. Southern blot analysis of DNA from leukemia cells was made using 4.5kb bcr-u and 1.5kb bcr-HE probes. Four patients with Ph negative CML had normal karyotypes. Among them, 3 had rearrangement of bcr, and 1 expected germ line pattern only. In the 4 patients with CML with unusual Ph translocation who had bcr rearrangement, one had a masked Ph chromosome originating from a translocation t(3;22) (p22;q11), the other three had one of the following complex Ph translocations: t(9;22;13) (q34;q11;q21), t(3;14;22) (p21;q32;q11) and t(X;9;22;12) (q22; q34; q11; q24). Our data confirmed that Ph negative CML could be divided into two different subsets: Ph-bcr+ CML and Ph-bcr-CML and that whatever the type of translocation may be, CML with unusual Ph translocation and Ph positive CML had a common molecular pathological basis.
对4例Ph阴性慢性粒细胞白血病(CML)患者和4例伴有异常Ph易位的CML患者进行了细胞遗传学和分子研究。通过R和G显带技术对骨髓细胞的直接制片和短期培养物进行染色体分析。使用4.5kb bcr-u和1.5kb bcr-HE探针,对白血病细胞的DNA进行Southern印迹分析。4例Ph阴性CML患者的核型正常。其中,3例bcr发生重排,1例仅呈现预期的种系模式。在4例伴有异常Ph易位且bcr重排的CML患者中,1例有一条源自t(3;22)(p22;q11)易位的隐匿性Ph染色体,另外3例有以下复杂Ph易位之一:t(9;22;13)(q34;q11;q21)、t(3;14;22)(p21;q32;q11)和t(X;9;22;12)(q22;q34;q11;q24)。我们的数据证实,Ph阴性CML可分为两个不同的亚组:Ph-bcr+CML和Ph-bcr-CML,并且无论易位类型如何,伴有异常Ph易位的CML和Ph阳性CML具有共同的分子病理基础。