Author/Authors :
Kawashima، نويسنده , , Hiroyuki and Ogose، نويسنده , , Akira and Gu، نويسنده , , Wenguang and Nishio، نويسنده , , Jun and Kudo، نويسنده , , Naoko and Kondo، نويسنده , , Naoki and Hotta، نويسنده , , Tetsuo and Umezu، نويسنده , , Hajime and Tohyama، نويسنده , , Tsuyoshi and Nishijima، نويسنده , , Hirokazu and Iwasaki، نويسنده , , Hiroshi and Endo، نويسنده , , Naoto، نويسنده ,
Abstract :
We established a novel human myxofibrosarcoma cell line NMFH-1 and analyzed it with spectral karyotyping and comparative genomic hybridization (CGH). NMFH-1 cells are composed of two different types of cells, small, spindle-shaped mononuclear cells and bizarre multinucleated giant cells, which were maintained in vitro over 200 passages. Xenografted tumor showed typical features of myxofibrosarcoma, which included bizarre multinucleated giant cells. Cytogenetic analyses revealed complex abnormalities, including a t(17;22)(q2?2;q13), which has been found in dermatofibrosarcoma protuberans. Subsequent reverse-transcription polymerase chain reaction revealed that the cell line did not have the COL1A1-PDGFB gene fusion. Significant gains of the 1q12∼q23 and 8q13∼qter regions and loss of the 9p21∼pter and 13q12 regions often found in MFH were observed by CGH analysis. We investigated the origin of multinucleated giant cells in xenografted tumor through DNA in situ hybridization. In this system, the human-specific Alu sequence and the mouse L1 sequence were used as specific cell markers of identity. In situ hybridization revealed neoplastic proliferation of the multinucleated giant cells of human origin.
