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两名慢性粒细胞白血病患者中的一种复杂的三向易位(4;9;22)

A three way complex translocation (4; 9; 22) in two patients with chronic myelocytic leukemia.

作者信息

Sheth Frenny J, Sheth Jayesh J, Verhest Alain

机构信息

FRIGE (Foundation for Research in Genetics and Endocrinology) Genetic Centre, 20/1, Bima Nagar, Satellite, Ahmedabad-380 015, India.

出版信息

J Cancer Res Ther. 2005 Apr-Jun;1(2):108-10. doi: 10.4103/0973-1482.16711.

Abstract

Chronic myeloid leukemia (CML) is genetically characterized by the reciprocal translocation of chromosome 9 and 22, t(9;22)(q34;q11) which results in the fusion of BCR/ABL gene observed on the derivative chromosome 22 called Philadelphia (Ph') chromosome. About 5-8% of Philadelphia positive patients with CML show various complex translocations involving third chromosome in addition to chromosome 9 and 22. In present report we discuss two cases with CML referred at our centre. At the time of initial diagnosis and after 9 months of treatment, one of the patients showed 100% presence of Philadelphia positive in bone marrow culture. During follow-up in an accelerated state, his cytogenetic study revealed a complex translocation (4;9;22)(q25;q34;q11) along with an additional Philadelphia and marker chromosome. The second patient showed a complex (4;9;22)(q25;q34;q11) translocation at the time of diagnosis. He was on hydroxyurea and his follow-up cytogenetic study after the course of chemotherapy showed no changes. Further confirmation of complex translocation was done by FISH study using bcr/abl and whole chromosome 9 probes. Though the additional genes involved in complex variant Ph' rearrangements have not been characterized, both patients are healthy till 3 to 5 years of initial diagnosis. This could be attributed to the benign effect resulted from reciprocal translocation with no loss or gain of the genetic material.

摘要

慢性粒细胞白血病(CML)的遗传学特征是9号和22号染色体相互易位,即t(9;22)(q34;q11),这导致在衍生的22号染色体(称为费城染色体(Ph'染色体))上观察到BCR/ABL基因融合。约5-8%的费城染色体阳性CML患者除9号和22号染色体外,还表现出涉及第三条染色体的各种复杂易位。在本报告中,我们讨论了在我们中心转诊的2例CML患者。在初次诊断时以及治疗9个月后,其中1例患者骨髓培养中费城染色体阳性率为100%。在加速期随访期间,他的细胞遗传学研究显示存在复杂易位(4;9;22)(q25;q34;q11),同时还有一条额外的费城染色体和一条标记染色体。第2例患者在诊断时显示存在复杂的(4;9;22)(q25;q34;q11)易位。他接受羟基脲治疗,化疗疗程后的随访细胞遗传学研究显示无变化。使用bcr/abl和9号全染色体探针进行的荧光原位杂交(FISH)研究进一步证实了复杂易位。尽管参与复杂变异Ph'重排的其他基因尚未明确,但这2例患者自初次诊断起3至5年一直健康。这可能归因于相互易位产生的良性效应,没有遗传物质的丢失或增加。

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