Characteristics of novel myeloid precursor cell line, PC-MDS, established from a bone marrow of the patient with therapy-related myelodysplastic syndrome

Leuk Res. 2007 Aug;31(8):1097-1105. doi: 10.1016/j.leukres.2007.01.012. Epub 2007 Mar 12.

Abstract

We report on characteristics of the first human cell line, PC-MDS, derived from a bone marrow of a patient with therapy-related myelodysplastic syndrome (t-MDS) who had no overt post-MDS leukemia. Classic cytology analyses, immunophenotyping, cytogenetic and molecular genetic procedures were used for characterization of the cell line. PC-MDS cells are positive for the expression of CD13, CD15, CD30, CD33, and CD45 antigen. Positive cytochemical staining and immunophenotype analyses indicated that PC-MDS cells have some characteristics of the early myeloid precursor cell. The karyotype analysis of PC-MDS cell line revealed various numerical and structural changes including those typically associated with t-MDS: del(5)(q13)[7], der(5)t(5;11)(p11;q11)[13], -7[6], del(7)(q31)[2], +20[3], -20[4]. Evaluation of methylation status in a promoter region of p15, p16 and MGMT genes showed biallelic hypermethylation pattern of 5' promoter region only in MGMT gene. PC-MDS is the first t-MDS derived cell line, and based on its immunological, cytogenetic and molecular characterization could be a new tool in evaluation of complex biology of MDS and a model for methylation studies.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antineoplastic Agents / therapeutic use
  • Bone Marrow / pathology*
  • Cyclin-Dependent Kinase Inhibitor p15 / genetics
  • Cyclin-Dependent Kinase Inhibitor p15 / metabolism
  • DNA Methylation
  • DNA Modification Methylases / genetics
  • DNA Repair Enzymes / genetics
  • Genes, T-Cell Receptor / genetics
  • Genes, p16
  • Humans
  • Immunoglobulin Variable Region / genetics
  • Immunophenotyping
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Myelodysplastic Syndromes / pathology*
  • Myeloid Progenitor Cells / pathology*
  • Polymerase Chain Reaction
  • Tumor Cells, Cultured
  • Tumor Suppressor Proteins / genetics

Substances

  • Antineoplastic Agents
  • Cyclin-Dependent Kinase Inhibitor p15
  • Immunoglobulin Variable Region
  • Tumor Suppressor Proteins
  • DNA Modification Methylases
  • MGMT protein, human
  • DNA Repair Enzymes