Literature DB >> 14734225

A chronic myelocytic leukemia case bearing deletions on the three chromosomes involved in a variant t(9;22;11).

Luisa Anelli1, Francesco Albano, Antonella Zagaria, Arcangelo Liso, Maria Grazia Roberti, Mariano Rocchi, Giorgina Specchia.   

Abstract

Genomic deletions on the derivative chromosomes bearing the reciprocal fusion gene have recently been reported in chronic myelocytic leukemia (CML). We here describe a CML case with a variant rearrangement t(9;22;11)(q34;q11;q13) showing the loss of chromosome 11 sequences in addition to der(9) deletions. Known tumor suppressor genes involved in apoptosis and in the control of cell proliferation were found to be mapped to the lost sequences. Our findings indicate that genomic deletions may occur also on the third derivative chromosome in variant t(9;22).

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Year:  2004        PMID: 14734225     DOI: 10.1016/s0165-4608(03)00246-2

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  2 in total

1.  Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements.

Authors:  Francesco Albano; Luisa Anelli; Antonella Zagaria; Nicoletta Coccaro; Paola Casieri; Antonella Russo Rossi; Laura Vicari; Vincenzo Liso; Mariano Rocchi; Giorgina Specchia
Journal:  Mol Cancer       Date:  2010-05-25       Impact factor: 27.401

2.  A novel t(9;22;11) translocation involving 11q24 in a patient with chronic myeloid leukemia: A case report.

Authors:  Jaehyeon Lee; Dal Sik Kim; Hye Soo Lee; Sam Im Choi; Yong Gon Cho
Journal:  Oncol Lett       Date:  2017-02-01       Impact factor: 2.967

  2 in total

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