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  • Digitale Medien  (4)
  • Immunofluorescence microscopy  (2)
  • Tumor suppressor gene  (2)
Materialart
  • Digitale Medien  (4)
Erscheinungszeitraum
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of cancer research and clinical oncology 106 (1983), S. 234-239 
    ISSN: 1432-1335
    Schlagwort(e): Osteosarcoma ; Collagen types ; Immunofluorescence microscopy ; Electron microscopy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Sixteen cases of typical highly malignant osteosarcoma were investigated by light, electron, and immunofluorescence microscopy to demonstrate the presence of collagen types I–III. It was shown that, in light-microscopically anaplastic areas of the tumor, collagen type III predominates, while only very few membranes of collagen type I are observed. Ultrastructurally, the cells are characterized by numerous free ribosomes in their cytoplasm and only a few membranes of granular endoplasmic reticulum (ER). In osteoblastic areas, collagen type I is increased, while type-III collagen is decreased. The cytoplasm of cells contains markedly more granular ER. An increasing mineralization of matrix is observed. In fibroblastic areas of the tumors, collagen types I and III are codistributed. Tumor cells have a fibroblast appearance with elongated nuclei and well developed granular ER. The chondroblastic areas, characterized by immature neoplastic cartilage, contain varying amounts of collagen type II. Chondroblast-like tumor cells have typical ring-shaped membranes of granular ER in their cytoplasm. The evidence of different collagen types in osteosarcomas lends additional support to the concept that a pluripotent mesenchymal cell is the stem cell of osteosarcomas.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Virchows Archiv 424 (1994), S. 357-360 
    ISSN: 1432-2307
    Schlagwort(e): Tumor suppressor gene ; p53 ; Macrophage ; Giant cell ; Cell cycle
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Accumulation of p53 has been reported in nearly all malignant human tumours. Macrophage derived giant cells of sarcoid granulomas in human lung tissue also show intense staining for p53 while normal alveolar macrophages remain unstained. Since sarcoid giant cells are not considered to be either pre-neoplastic nor to exhibit p53 gene mutations, two different physiological functions of p53 may be illustrated. Alveolar macrophages were isolated from rat lungs and cultured in vitro. Accumulation of p53 was observed by indirect immunohistochemistry after application of polyclonal rabbit serum directed against murine p53 (CM5). Antiproliferating cell nuclear antigen (PCNA) antibodies were used to study DNA synthesis. Most of the multinucleated giant cells derived from macrophages accumulated p53 in the cytoplasm, while only few nuclei were stained. PCNA was found in most giant cells nuclei. However, PCNA positivity was visible in few mononucleated macrophages. Isolated alveolar macrophages in vitro clearly divide and since nuclear division is a late event in the cell cycle, p53 may be involved in G1/S-control and in other cell-cycle-checkpoints between mitosis and cytokinesis.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Der Pathologe 15 (1994), S. 321-330 
    ISSN: 1432-1963
    Schlagwort(e): Schlüsselwörter Lunge ; Tumorsuppressorgene ; Onkogene ; Krebsentstehung ; Key words Lung ; Tumor suppressor gene ; Oncogene ; Cancerogenesis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Beschreibung / Inhaltsverzeichnis: Summary The recent results obtained from investigations based on molecular biological techniques have led to a better understanding of recurrent genetic causes important for the pathogenesis of tumors. Several genes have been identified as being involved in the development of cancer. In many cases, the activation of oncogenes or the inactivation of tumor-suppressor genes is the predominant reason for cancerogenic cell transformation. Functional dysregulation is frequently the consequence of mutations, resulting in an alteration of the primary structure of the DNA. As our understanding of the nature, function, and interaction of these genes evolves, new opportunities for early diagnosis, classification, prevention, and treatment of malignant tumors will arise. The present report summarizes the current molecular biological aspects of several oncogenes (erbB, ras, myc, raf, fos, jun, bcl, mdm 2, myb, kit CSF1R, met) and tumor suppressor genes (p 53, rb, mts) involved in lung-cancer development with respect to the pathology of lung tumors, including the importance of these genes as far as the clinical course of the disease is concerned.
    Notizen: Zusammenfassung Die Fortschritte der letzten Jahre, insbesondere auf dem Gebiet der molekularen Genetik, haben wesentlich zum besseren Verständnis der Genese und Progression von Tumoren beigetragen. Nach dem heutigen Erkenntnisstand besitzen morphologisch als tumorös charakterisierte Zellen unterschiedliche genetische Alterationen. Im Verlauf der Tumorprogression kann es zusätzlich zur Akkumulation weiterer genetischer Alterationen kommen. Nach den heute vorherrschenden Arbeitshypothesen sind für eine bösartige Entartung von Zellen 3–10, in der Regel unabhängige genetische Alterationen Voraussetzung. Die Veränderungen in der Erbsubstanz betreffen überwiegend solche Gene, die direkt oder indirekt das Wachstum, die Proliferation oder die Differenzierung der Zelle regulieren. Die für die Entstehung von Tumoren verantwortlichen Gene werden dabei in die Klassen der Onkogene und der Tumor Suppressor Gene oder Anti-Onkogene eingeteilt. Bei Onkogenen führt definitionsgemäß erst eine (Über-) Aktivierung des betreffenden (Proto-) Onkogens zu einer Entartung der Zelle – bei Tumor-Suppressor-Genen ist eine (Teil-) Inaktivierung des Gens Voraussetzung für eine Transformation der Zelle. Neben chromosomalen Abnormalitäten, die in der Regel größere Genomabschnitte betreffen und zum Teil bereits auf lichtmikroskopischer Ebene diagnostiziert werden, spielen bei der Genese und Progression von Lungentumoren gerade genetische Alterationen in Onko- oder Tumor-Suppressor-Genen eine zentrale Rolle. Die vorliegende Übersicht faßt Erkenntnisse über die Gene zusammen, die heute als Faktoren bei der Kanzerogenese von Lungentumoren Bedeutung erlangt haben.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of cancer research and clinical oncology 104 (1982), S. 171-180 
    ISSN: 1432-1335
    Schlagwort(e): Ewing's sarcoma ; Type IV collagen ; Factor-VIII-associated protein ; Endothelial differentiation ; Electron microscopy ; Immunofluorescence microscopy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Six cases of Ewing's sarcoma were investigated by electron and immunofluorescence microscopy. A layer of basement membrane-like deposits was found between typical principal and secondary tumor cells. To clarify the nature of these ultrastructural deposits, antibodies against collagen type IV were applied to frozen sections of corresponding tumor tissue. This reaction revealed type IV collagen as a regular component of basement membranes in nonneoplastic tumor capillaries, but it was equally able to localize collagen type IV between single tumor cells in capillary-free areas. With the same method, factor-VIII-associated protein, predominantly found in endothelial cells, could be demonstrated in some tumor cells. These results demonstrate that, in addition to anaplastic cells, some tumor cells are found in Ewing's sarcoma that share certain differentiating features with the endothelial cell.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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