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Chondrocytic differentiation of peripheral neuroectodermal tumor cell line in nude mouse xenograft.

Abstract
We have established a cell line (KU-SN) from a peripheral neuroectodermal tumor originating in the left scapula of a 4-year-old girl. The original tumor was immunoreactive with antibodies for neurofilament proteins, neuron-specific enolase, vimentin, S100 protein, and beta 2-microglobulin. Dense core granules, 50-150 nm in diameter, were identified by electron microscopy. The cell line was established from tumor cells in metastatic lung fluid. KU-SN cells were immunoreactive with the antibodies for neurofilament proteins, vimentin, neuron-specific enolase, S100 protein, glial fibrillary acidic protein, cytokeratin, and carcinoembryonic antigen. Besides these neuronal features, KU-SN cells express type 2 collagen and insulin-like growth factor 1 receptor. The addition of insulin-like growth factor 1 (100 ng/ml) increased the growth rate of KU-SN cells 2.1-fold over control. Some cells were positive for Alcian blue and alkaline phosphatase staining. Cytogenetic analysis of KU-SN cells disclosed a reciprocal chromosomal translocation [t(11,22)]. Northern blot analysis of KU-SN cells demonstrated amplified expression of the c-myc gene but not the N-myc gene. When tumor cells were transplanted into nude mice, cartilage was formed. The cartilage was immunoreactive with the antibody for HLA-ABC, indicating that it was derived from the tumor cells, not from mouse tissue. Chondrocytic differentiation was not observed in xenografts of Ewing's sarcoma cell lines SK-ES or RD-ES or the peripheral neuroectodermal tumor cell line SK-N-MC. These results indicate that KU-SN cells represent primitive neural crest cells having the potential for chondrocytic differentiation.
AuthorsJ Goji, K Sano, H Nakamura, H Ito
JournalCancer research (Cancer Res) Vol. 52 Issue 15 Pg. 4214-20 (Aug 01 1992) ISSN: 0008-5472 [Print] United States
PMID1379122 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Neurofilament Proteins
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • Transforming Growth Factor beta
  • RNA
  • Insulin-Like Growth Factor I
  • Collagen
Topics
  • Animals
  • Base Sequence
  • Bone Neoplasms (genetics, pathology, ultrastructure)
  • Cartilage (cytology, pathology)
  • Cell Differentiation
  • Cell Division (drug effects)
  • Cell Line
  • Child, Preschool
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 22
  • Collagen (genetics)
  • Culture Techniques (methods)
  • Cytoplasmic Granules (ultrastructure)
  • Exons
  • Female
  • Genes, myc
  • Humans
  • Immunohistochemistry
  • Insulin-Like Growth Factor I (pharmacology)
  • Mice
  • Mice, Nude
  • Molecular Sequence Data
  • Neoplasm Transplantation
  • Neoplasms, Germ Cell and Embryonal (genetics, pathology, ultrastructure)
  • Neurofilament Proteins (analysis)
  • Oligodeoxyribonucleotides
  • Polymerase Chain Reaction (methods)
  • RNA (genetics, isolation & purification)
  • RNA, Messenger (analysis, genetics)
  • Transforming Growth Factor beta (pharmacology)
  • Translocation, Genetic
  • Transplantation, Heterologous

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