Establishment of a novel childhood acute myeloid leukaemia cell line, KOPM‐88, containing partial tandem duplication of the MLL gene and an in vivo model for childhood acute myeloid leukaemia using NOD/SCID mice

• Published in: British journal of haematology 2007-05, Vol.137 (3), p.221-232
• Main Authors: Hayashi, Mutsumi, Kondoh, Kensuke, Nakata, Yuji, Kinoshita, Akitoshi, Mori, Taijiro, Takahashi, Takao, Sakamoto, Michi‐ie, Yamada, Taketo
• Format: Article
• Language: English
• Subjects: animal model; Animals; Antigens, Surface - immunology; Biological and medical sciences; Cell Division - immunology; cell line; Cell Line, Tumor; Cell Transplantation - methods; Child; childhood acute myeloid leukaemia; Cytokines - immunology; Disease Models, Animal; Fatal Outcome; Flow Cytometry - methods; Gene Duplication; Gene Rearrangement - genetics; Hematologic and hematopoietic diseases; Histone-Lysine N-Methyltransferase; Humans; In Situ Hybridization, Fluorescence - methods; Leukemia, Myeloid, Acute - genetics; Leukemia, Myeloid, Acute - immunology; Leukemia, Myeloid, Acute - pathology; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis; Male; Medical sciences; Mice; Mice, Inbred NOD; Mice, SCID; MLL gene; Myeloid-Lymphoid Leukemia Protein - genetics; partial tandem duplication; Polymerase Chain Reaction - methods; Tandem Repeat Sequences - genetics
• ISSN: 0007-1048; 1365-2141
• DOI: 10.1111/j.1365-2141.2007.06553.x

Summary MLL gene rearrangement is common in both adult and childhood acute myeloid leukaemia (AML), and its role in oncogenesis has been investigated. While over 50 translocated‐partner genes have been identified so far, few studies have detailed the molecular mechanism of partial tandem duplication (PTD) of the MLL gene. The prognostic impact and contribution to leukaemogenesis of MLL‐PTD, especially in childhood cases, remain unknown. We have established a novel cell line containing MLL‐PTD derived from an 11‐year‐old patient with AML and designated as KOPM‐88. KOPM‐88 cells exhibited certain characteristics associated with the myeloid lineage including abundant primary granules in the cytoplasm and the expression of myeloperoxidase. The cell growth of KOPM‐88 was cytokine independent but was accelerated by granulocyte colony‐stimulating factor and granulocyte‐macrophage colony‐stimulating factor. MLL‐PTD of exon 2 to exon 6 and exon 2 to exon 8 was revealed using Southern blotting, fluorescence in situ hybridisation, and reverse transcription polymerase chain reaction/DNA sequencing. Furthermore, non‐obese diabetic/severe combined immunodeficient mice inoculated with KOPM‐88 cells exhibited leukaemic infiltrations in the bone marrow and hemiparalysis because of compression myelopathy. This is the first report of an in vivo animal model exhibiting the systemic involvement of childhood AML containing MLL‐PTD. KOPM‐88 cells and our murine model may be useful for investigating the pathogenesis of childhood AML associated with MLL gene rearrangement.