Threeway Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylateresistant chronic myeloid leukemia patient

Author: AlAchkar Walid   Wafa Abdulsamad   Ikhtiar Adnan   Liehr Thomas  

Publisher: Spandidos Publications

ISSN: 1792-1074

Source: Oncology Letters, Vol.5, Iss.5, 2013-05, pp. : 1656-1658

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

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 510% of CML cases. In the present study, a novel case of a Ph chromosomepositive CML in the chronic phase (CP) is reported, with a threeway 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.