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Absence of IFNA and IFNB genes from human malignant glioma cell lines and lack of correlation with cellular sensitivity to interferons.
Miyakoshi, J; Dobler, K D; Allalunis-Turner, J; McKean, J D; Petruk, K; Allen, P B; Aronyk, K N; Weir, B; Huyser-Wierenga, D; Fulton, D.
Afiliação
  • Miyakoshi J; Department of Medicine, Cross Cancer Institute, Edmonton, Alberta, Canada.
Cancer Res ; 50(2): 278-83, 1990 Jan 15.
Article em En | MEDLINE | ID: mdl-2295067
ABSTRACT
We report that 5 of 19 human malignant glioma cell lines have neither interferon alpha (IFNA) nor interferon beta (IFNB) genes that are detectable by Southern blotting. Of 5 other of these malignant glioma lines that have a single IFNB gene copy, 3 lack the IFNA genes entirely and two have one copy. One of the lines that lacks the IFNA genes entirely but has one copy of the IFNB gene has a rearrangement near the IFNB gene that is most easily interpreted as an insertion of a large segment of DNA (at least 50 kilobases) the 3' end of which is less than 1.3 kilobases 5' to the known regulatory sequences of the IFNB gene. In spite of the rearrangement, IFNB-specific RNA is highly inducible in this line by poly(I)-poly(C). The ability of interferon alpha or interferon beta to inhibit cell growth does not depend upon the presence or absence of the respective gene. This finding adds solid tumors to those tumor cell lines (acute lymphocytic leukemia, chronic myelogeneous leukemia) previously determined to lack the IFNA and IFNB genes (Diaz et al., Proc. Natl. Acad. Sci. USA, 855259-5263, 1988).
Assuntos
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Base de dados: MEDLINE Assunto principal: Interferon Tipo I / Deleção Cromossômica / Glioma Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 1990 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Interferon Tipo I / Deleção Cromossômica / Glioma Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 1990 Tipo de documento: Article