UMMS Affiliation

Worcester Foundation for Biomedical Research; Cancer Center; Department of Neurology; Department of Biochemistry and Molecular Pharmacology; Department of Surgery

Date

2-1-1997

Document Type

Article

Subjects

Animals; Glioma; Male; Neoplasm Invasiveness; Proto-Oncogene Proteins; Rats; Rats, Inbred WKY; Receptor Protein-Tyrosine Kinases; Receptor, trkA; Receptors, Nerve Growth Factor; Tumor Cells, Cultured

Disciplines

Biochemistry, Biophysics, and Structural Biology | Medical Cell Biology | Molecular and Cellular Neuroscience | Neurology | Surgery

Abstract

We stably expressed the nerve growth factor receptor trkA or a truncated trkA lacking the kinase domain (trkA delta) in a highly tumorigenic rat glioma cell line, C6. Survival of rats with large intrastriatal inocula of C6trkA cells was significantly longer than for rats bearing C6 or C6trkA delta cells. Histological studies revealed that C6trkA cells were much less invasive than C6 or C6trkA delta cells and had a greater rate of apoptosis. There was no apparent induction of differentiation of C6 cells by trkA. Therefore, unlike what is observed in neuroblastomas, trkA decreases tumorigenicity by modulating invasiveness and tumor cell death independent of inducing differentiation. This novel mechanism suggests a new therapeutic strategy for malignant gliomas.

Rights and Permissions

Citation: Cancer Res. 1997 Feb 1;57(3):532-6.

Related Resources

Link to article in PubMed

Journal Title

Cancer research

PubMed ID

9012486

 
 

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