t(10;11)(p13-14;q14-21): a new recurrent translocation in T-cell acute lymphoblastic leukemias. Groupe Français de Cytogénétique Hématologique (GFCH)

Genes Chromosomes Cancer. 1991 Nov;3(6):411-5.

Abstract

A workshop held by the "Groupe Français de Cytogénétique Hématologique" has identified a t(10;11)(p13-14;q14-21) in four acute lymphoblastic leukemias of T-cell lineage. The immunophenotypes were consistent with immature thymocytes. This translocation is therefore a new candidate for a recurrent translocation in early T-cell leukemia. A similar translocation has been reported as a rare change in early pre-B lymphoid leukemias and also in myeloid leukemias. It is not known whether the similar cytogenetic changes involve different molecular breakpoints or whether the same rearrangement affects a multipotential stem cell capable of lymphoid and myeloid differentiation.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / analysis
  • Antigens, Neoplasm / analysis
  • Biomarkers, Tumor
  • Child
  • Chromosomes, Human, Pair 10 / ultrastructure*
  • Chromosomes, Human, Pair 11 / ultrastructure*
  • Female
  • Genetic Markers
  • Humans
  • Immunophenotyping
  • Leukemia-Lymphoma, Adult T-Cell / genetics*
  • Leukemia-Lymphoma, Adult T-Cell / immunology
  • Male
  • Neoplastic Stem Cells / immunology
  • Neoplastic Stem Cells / ultrastructure
  • Oncogenes
  • Translocation, Genetic*

Substances

  • Antigens, CD
  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • Genetic Markers