[The role of interferons in neuroblastoma. 1: Antiproliferative effects]. 1990

G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
Univ. Kinderklinik Tübingen, Abt. Hämatologie und Onkologie.

Antiproliferative effects of interferon alpha, beta and gamma were investigated on several human neuroblastoma cell lines using the soft agar colony forming assay and the MTT-test. Investigations were carried out in order to prove whether there is any relationship between antiproliferative effects, inhibition of N-myc expression and the 2-5A system. Growth of neuroblastoma cells was inhibited by all three kinds of interferons in a concentration-dependent manner, however, rather high concentrations were necessary in some cell lines. Expression of N-myc oncogen was not inhibited by interferon-beta and no relationship between antiproliferative effects and the 2-5A system was observed. A vector containing a small N-myc fragment in antisense direction was constructed and transferred into the interferon insensitive human neuroblastoma cell line LS. After transformation, LS cells became sensitive to interferon beta: Proliferation as well as N-myc expression were inhibited and these processes are most probably associated with activation of the 2-5A system.

UI MeSH Term Description Entries
D007372 Interferons Proteins secreted by vertebrate cells in response to a wide variety of inducers. They confer resistance against many different viruses, inhibit proliferation of normal and malignant cells, impede multiplication of intracellular parasites, enhance macrophage and granulocyte phagocytosis, augment natural killer cell activity, and show several other immunomodulatory functions. Interferon
D009447 Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) Neuroblastomas
D011518 Proto-Oncogene Proteins Products of proto-oncogenes. Normally they do not have oncogenic or transforming properties, but are involved in the regulation or differentiation of cell growth. They often have protein kinase activity. Cellular Proto-Oncogene Proteins,c-onc Proteins,Proto Oncogene Proteins, Cellular,Proto-Oncogene Products, Cellular,Cellular Proto Oncogene Proteins,Cellular Proto-Oncogene Products,Proto Oncogene Products, Cellular,Proto Oncogene Proteins,Proto-Oncogene Proteins, Cellular,c onc Proteins
D011994 Recombinant Proteins Proteins prepared by recombinant DNA technology. Biosynthetic Protein,Biosynthetic Proteins,DNA Recombinant Proteins,Recombinant Protein,Proteins, Biosynthetic,Proteins, Recombinant DNA,DNA Proteins, Recombinant,Protein, Biosynthetic,Protein, Recombinant,Proteins, DNA Recombinant,Proteins, Recombinant,Recombinant DNA Proteins,Recombinant Proteins, DNA
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D002460 Cell Line Established cell cultures that have the potential to propagate indefinitely. Cell Lines,Line, Cell,Lines, Cell
D005784 Gene Amplification A selective increase in the number of copies of a gene coding for a specific protein without a proportional increase in other genes. It occurs naturally via the excision of a copy of the repeating sequence from the chromosome and its extrachromosomal replication in a plasmid, or via the production of an RNA transcript of the entire repeating sequence of ribosomal RNA followed by the reverse transcription of the molecule to produce an additional copy of the original DNA sequence. Laboratory techniques have been introduced for inducing disproportional replication by unequal crossing over, uptake of DNA from lysed cells, or generation of extrachromosomal sequences from rolling circle replication. Amplification, Gene
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014407 Tumor Cells, Cultured Cells grown in vitro from neoplastic tissue. If they can be established as a TUMOR CELL LINE, they can be propagated in cell culture indefinitely. Cultured Tumor Cells,Neoplastic Cells, Cultured,Cultured Neoplastic Cells,Cell, Cultured Neoplastic,Cell, Cultured Tumor,Cells, Cultured Neoplastic,Cells, Cultured Tumor,Cultured Neoplastic Cell,Cultured Tumor Cell,Neoplastic Cell, Cultured,Tumor Cell, Cultured
D014410 Tumor Stem Cell Assay A cytologic technique for measuring the functional capacity of tumor stem cells by assaying their activity. It is used primarily for the in vitro testing of antineoplastic agents. Clonogenic Cell Assay, Tumor,Colony-Forming Units Assay, Tumor,Neoplasm Stem Cell Assay,Stem Cell Assay, Tumor,Colony Forming Units Assay, Tumor

Related Publications

G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
February 1995, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
December 1985, Virology,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
January 1984, Journal of interferon research,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
January 1981, Methods in enzymology,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
January 1988, Urologia internationalis,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
January 1989, Virologie,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
December 1984, Laboratory investigation; a journal of technical methods and pathology,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
January 1985, Voprosy virusologii,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
December 1986, Journal of interferon research,
G Bruchelt, and R Handgretinger, and K Schilbach-Stückle, and F H Schilling, and P Pollwein, and M Schwab, and J Treuner, and D Niethammer
January 1987, Voprosy virusologii,
Copied contents to your clipboard!