作者: Makoto Emoto , Hiroshi Iwasaki , Masahiro Kikuchi , Koichi Shirakawa
DOI: 10.1002/1097-0142(19930515)71:10<3065::AID-CNCR2820711029>3.0.CO;2-D
关键词: Cell culture 、 Mesenchymal stem cell 、 Clone (B-cell biology) 、 Sarcoma 、 Monoclonal 、 Biology 、 Molecular biology 、 Pathology 、 Mixed Müllerian tumor 、 Cell type 、 Adenocarcinoma 、 Cancer research 、 Oncology
摘要: Background. To elucidate the relationship between epithelial and mesenchymal elements of malignant mixed Mullerian tumors (MMMT), authors examined biologic properties two clones different cell types (designated as FU-MMT-2-C1 FU-MMT-2-S1) established from a uterine MMMT line (FU-MMT-2), which they previously have reported. Methods Results. By morphologic immuno-cytochemical analyses, exhibited features adenocarcinoma cells, whereas FU-MMT-2-S1 showed characteristics sarcoma cells with myogenic differentiation. Some at confluence differentiated spontaneously into in vitro. In addition, transitional-type sarcomatous were observed areas differentiation by light electron microscopic study. Ultrastructurally, represented biphasic consisting features, proved to coexpress epithelial, mesenchymal, muscle markers double immunoenzymatic staining. However, no differentiations apparent clone FU-MMT-2-S1. produced tumor nude mice, histologic study mixture that resembled original tumor. Cytogenetic studies demonstrated these monoclonal origin because presence common karyotypic abnormalities both cells. amplified (approximately fourfold eightfold) c-myc oncogene was found cloned cells. Conclusions. The current results strongly support theory single suggest originated primitive capable differentiating or elements.