Z-138: a new mature B-cell acute lymphoblastic leukemia cell line from a patient with transformed chronic lymphocytic leukemia

Leuk Res. 1998 Apr;22(4):341-53. doi: 10.1016/s0145-2126(97)00191-4.

Abstract

We describe a new mature B-cell acute lymphoblastic leukemia (ALL) cell line designated Z-138 that was derived from a patient with chronic lymphocytic leukemia (CLL) whose disease underwent transformation to a rare, aggressive form of mature B-cell ALL. This cell line has an L3 morphology, ultrastructural characteristics of lymphoblasts, B-lineage surface markers and an immunoglobulin heavy-chain gene rearrangement identical to the rearrangement observed in the patient's blasts from whom the cell line was derived. Z-138 cells produce granulocyte-macrophage colony-stimulating factor (GM-CSF) and high levels of granulocyte-CSF (G-CSF), but they do not exhibit a proliferative response to either cytokine. Both the patient's lymphoblasts and Z-138 cells exhibited cytogenetic abnormalities including t(8;14), t(14;18) and a chromosome 11 abnormality similar to the t(11;14) of the parental cells, resulting in marked overexpression of cyclin D1 (BCL-1 (PRAD1)) mRNA in Z-138 cells. Since these karyotypic anomalies have been associated with low grade (t(14;18)), intermediate grade (t(11;14)) and high grade (t(8;14)) lymphomas, their development may be involved in the unusual aggressive transformation of this patient's CLL.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Blotting, Southern
  • Bone Marrow Cells / pathology
  • Burkitt Lymphoma / etiology*
  • Burkitt Lymphoma / immunology
  • Burkitt Lymphoma / pathology*
  • Cell Transformation, Neoplastic / pathology*
  • Cell Transformation, Viral
  • Chromosome Aberrations / genetics*
  • Chromosomes, Human, Pair 9 / genetics*
  • Clone Cells / chemistry
  • DNA / analysis
  • Fusion Proteins, bcr-abl / biosynthesis
  • Gene Rearrangement, B-Lymphocyte, Heavy Chain / genetics
  • Granulocyte Colony-Stimulating Factor / biosynthesis
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Herpesvirus 4, Human / isolation & purification
  • Humans
  • Immunoglobulin J-Chains / genetics
  • Immunophenotyping
  • Interleukin-1 / biosynthesis
  • Interleukin-6 / biosynthesis
  • Karyotyping
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology*
  • Lymphocyte Activation / drug effects
  • Male
  • Microscopy, Electron
  • RNA / analysis
  • Transforming Growth Factor beta / biosynthesis
  • Tumor Cells, Cultured / cytology*
  • Tumor Cells, Cultured / physiology
  • Tumor Cells, Cultured / virology
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Immunoglobulin J-Chains
  • Interleukin-1
  • Interleukin-6
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Granulocyte Colony-Stimulating Factor
  • RNA
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • DNA
  • Fusion Proteins, bcr-abl