Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Gliosarcoma: an immunohistochemical study.

J W Grant1, P V Steart, A Aguzzi

  • 1Institut für Pathologie, Universitäts-Krankenhaus, Zürich, Switzerland.

Acta Neuropathologica
|January 1, 1989
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Analysis of co-isogenic prion protein deficient mice reveals behavioral deficits, learning impairment, and enhanced hippocampal excitability.

BMC biology·2022
Same author

Gastric metastasis from cervix carcer: a case report.

Pathologica·2018
Same author

Decreased NOX2 expression in the brain of patients with bipolar disorder: association with valproic acid prescription and substance abuse.

Translational psychiatry·2017
Same author

Recurrent intracerebral haemorrhage after coitus: a case report of sporadic cerebral amyloid angiopathy in a younger patient.

European journal of neurology·2012
Same author

Recent developments in the pathogenesis, diagnosis, and therapy of prion diseases.

Dialogues in clinical neuroscience·2011
Same author

Prions: from neurografts to neuroinvasion.

Methods in molecular medicine·2011
Same journal

Mutation-specific neuropathologic signatures in MAPT-associated frontotemporal lobar degeneration.

Acta neuropathologica·2026
Same journal

Molecular changes during AT/RT progression associated with epithelial-mesenchymal transition and extracellular matrix changes.

Acta neuropathologica·2026
Same journal

Prion-like transmission and propagation of human β-amyloid to the bank vole rodent model.

Acta neuropathologica·2026
Same journal

Inhibition of tRNA fragments dysregulated in human mTLE exacerbates pathology and seizure activity.

Acta neuropathologica·2026
Same journal

VMA21 deficiency leads to autophagic dysregulation and altered vesicle trafficking in X-linked myopathy with excessive autophagy.

Acta neuropathologica·2026
Same journal

Donor-specific pathological features associate with genetic background, lesion type distribution, and clinical heterogeneity in multiple sclerosis.

Acta neuropathologica·2026
See all related articles

Gliosarcomas, tumors with neuro-ectodermal and mesenchymal parts, likely originate from fibroblasts or mesenchymal cells. Immunohistochemistry reveals distinct glial and sarcoma components, supporting a fibroblast origin for the sarcomatous element.

Area of Science:

  • Oncology
  • Pathology
  • Immunohistochemistry

Background:

  • Gliosarcomas are rare brain tumors with both glial and mesenchymal components.
  • The histogenesis of the sarcomatous element in gliosarcomas remains a subject of debate.
  • Previous studies suggested various origins, including endothelial, adventitial fibroblasts, or histiocytes.

Purpose of the Study:

  • To investigate the origin of the sarcomatous component in gliosarcomas.
  • To utilize a panel of antibodies for immunohistochemical analysis.
  • To compare the immunohistochemical profile with known cellular origins.

Main Methods:

  • Examined eight gliosarcomas using ten monoclonal and polyclonal antibodies.
  • Assessed expression of glial fibrillary acid protein, factor 8-related antigen, Ulex europeus agglutinin, vimentin, fibronectin, desmin, neurofilament protein, alpha-1-antitrypsin, alpha-1-chymotrypsin, and MAC 387.

Related Experiment Videos

  • Analyzed the immunohistochemical staining patterns in both gliomatous and sarcomatous areas.
  • Main Results:

    • Glial fibrillary acid protein expression was confined to the gliomatous component.
    • Factor 8-related antigen and Ulex europeus agglutinin stained only vascular endothelium, not tumor cells.
    • Vimentin and fibronectin were extensively expressed in sarcomatous areas.
    • Alpha-1-antitrypsin and alpha-1-chymotrypsin were expressed in many sarcoma cells, with some co-expressing the monocyte/macrophage marker MAC 387.
    • A storiform pattern was observed in four cases.

    Conclusions:

    • The immunohistochemical findings suggest that the sarcomatous component of gliosarcomas originates from fibroblasts or pluripotent mesenchymal cells.
    • The results support analogies with fibrous histiocytomas, which are thought to arise from fibroblasts or perivascular adventitial cells.
    • The distinct expression patterns differentiate the glial and sarcomatous elements, clarifying histogenesis.