Rajasekariah P, Garson O M
Pathology. 1981 Apr;13(2):197-203. doi: 10.3109/00313028109081660.
The bone marrow chromosomes of 15 patients with Ph1+ chronic granulocytic leukaemia were studied, using both G- and C-banding. In all cases the Ph1 chromosome was formed by the translocation between chromosomes 9 and 22 and the material from chromosome 22 was found to be translocated randomly onto one or other of the pair of 9 chromosomes. Preliminary results suggest that when the translocation was on the 9 chromosome having a smaller C-band, additional abnormalities occurred in blastic transformation, whereas when the 9 chromosome with the larger C-band was involved in the translocation, additional abnormalities were not found in blastic transformation. These observations require confirmation from a larger series. C-banding also showed that there was a greatly increased heteromorphism of the C-band areas of the chromosome pair 9 in this disease, and an increased heteromorphism in the C-bands of chromosome pair 1, when compared with a control group.
对15例Ph1+慢性粒细胞白血病患者的骨髓染色体进行了研究,采用了G带和C带技术。在所有病例中,Ph1染色体是由9号和22号染色体之间的易位形成的,并且发现22号染色体的物质随机易位到一对9号染色体中的一条上。初步结果表明,当易位发生在C带较小的9号染色体上时,在原始细胞转化时会出现额外的异常,而当易位涉及C带较大的9号染色体时,在原始细胞转化中未发现额外的异常。这些观察结果需要更多病例的证实。C带还显示,与对照组相比,该疾病中9号染色体对的C带区域的异质性大大增加,1号染色体对的C带异质性也增加。