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Two Cases of Translocation t(3;6)(p14;p22): A Non Random Chromosomal Abnormality?

M Lessard1, G Flandrin1, F Valensi1

  • 1a Laboratoire Central d'Hématologie, Hopital Saint-Louis, Paris, France.

Leukemia & Lymphoma
|July 28, 2016
PubMed
Summary

This study identifies a rare chromosomal translocation, t(3;6)(p14;p22), in two leukemia patients. This finding suggests the translocation is nonrandom and linked to environmental exposures and secondary aberrations.

Keywords:
CMLacute megakaryoblastic leukemianon random chromosomal abnormalityt(3;6)translocation

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Area of Science:

  • Cytogenetics
  • Oncology
  • Molecular Biology

Background:

  • The short arm of chromosome 6 is implicated in chromosomal rearrangements in myelodysplastic syndromes/acute myeloid leukemia (MDS/ANLL) post-treatment.
  • Previous studies suggest a link between chemotherapy/radiotherapy and secondary chromosomal abnormalities in leukemia.

Purpose of the Study:

  • To report and analyze two novel cases of the uncommon chromosomal translocation t(3;6)(p14;p22).
  • To compare these cases with existing literature to determine if t(3;6) is a nonrandom event associated with specific exposures or genetic alterations.

Main Methods:

  • Karyotyping and chromosomal analysis were performed on bone marrow samples from two leukemia patients.
  • Case details, including medical history, treatment, and cytogenetic findings, were collected and compared with published data.

Main Results:

  • Two patients presented with t(3;6)(p14;p22), one with acute megakaryoblastic leukemia and another with chronic myeloid leukemia.
  • Both patients had a history of occupational exposure or prior treatment (chemo/radiotherapy, Hydroxyurea).
  • The translocation was associated with other secondary aberrations, including del(5)(q14q31) and -7, and involved known oncogene (pim-1) and fragile sites (3p14).

Conclusions:

  • The uncommon translocation t(3;6)(p14;p22) appears to be nonrandom.
  • This translocation may be a marker for secondary leukemia, potentially linked to mutagenic exposures and specific genetic alterations.