首页> 美国卫生研究院文献>Oncology Letters >Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patient
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Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patient

机译:三向费城易位t(9; 10; 22)(q34; p11.2; q11.2)是甲磺酸伊马替尼耐药的慢性粒细胞白血病的继发性异常

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摘要

Chronic myelogenous leukemia (CML) is characterized by the Philadelphia (Ph) chromosome created by the reciprocal translocation t(9:22)(q34;q11), resulting in the chimeric gene breakpoint cluster region (BCR)-Abelson (ABL). Variant Ph chromosome translocations involving chromosomes other than 9 and 22 occur in 5–10% of CML cases. In the present study, a novel case of a Ph chromosome-positive CML in the chronic phase (CP) is reported, with a three-way Ph translocation involving three chromosomal regions, 9q34, 10p11.2 and 22q11.2, in addition to the loss of the Y chromosome, where the latter was a secondary abnormality. Since the majority of CML cases are currently treated with imatinib, variant rearrangements generally have no specific prognostic significance, although the mechanisms involved in resistance to therapy have yet to be investigated. The underlying mechanisms and prognostic implications of these cytogenetic abnormalities are discussed in the present study.
机译:慢性粒细胞性白血病(CML)的特征是由相互易位t(9:22)(q34; q11)创建的费城(Ph)染色体,导致嵌合基因断点簇区域(BCR)-Abelson(ABL)。 Ph染色体易位变异涉及9和22以外的染色体,发生在5-10%的CML病例中。在本研究中,报告了一个慢性期(CP)的Ph染色体阳性CML的新病例,除了三个染色体区域(9q34、10p11.2和22q11.2)外,还发生了三向Ph移位。 Y染色体的丢失,后者是继发性异常。由于目前大多数的CML病例都接受伊马替尼治疗,因此变异重排通常没有特异性的预后意义,尽管尚需研究抗药性的机制。这些细胞遗传学异常的潜在机制和预后意义在本研究中进行了讨论。

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