A novel myeloid cell line, Marimo, derived from therapy-related acute myeloid leukemia during treatment of essential thrombocythemia: consistent chromosomal abnormalities and temporary C-MYC gene amplification

Cancer Genet Cytogenet. 1998 Jan 1;100(1):21-4. doi: 10.1016/s0165-4608(97)00017-4.

Abstract

A novel myeloid leukemia cell line, Marimo, was established from bone marrow cells of a patient with secondary acute myeloid leukemia (AML) that had developed during the treatment of essential thrombocythemia (ET) with busulfan. Karyotype at the ET phase was 46,XX,der(15)t(1;15) (q23;p12-13), but at the blastic phase changed to 44,XX,-5,del(8)(q22), add(17)(p11),+18, psu dic(18;9) (q23;p21) x 2 lacking t(1;15). In Marimo cells, C-MYC gene was temporarily amplified by double-minutes (dmin) but disappeared at 33 months, whereas t(10;14;11)(q22;q32;q13) and t(10;14)(q22;q32) were added in vitro psu dic(18;9) x 2 and add(17)(p11) were consistently found throughout the culture. These results suggest that this AML clone is not derived from ET but rather is therapy-related.

Publication types

  • Case Reports

MeSH terms

  • Cell Line
  • Chromosome Aberrations*
  • Female
  • Gene Amplification*
  • Genes, myc*
  • Humans
  • Leukemia, Myeloid, Acute / genetics*
  • Middle Aged
  • Neoplasms, Second Primary / genetics*
  • Thrombocytosis / drug therapy*