Co-expression of Fas and Fas ligand in human non-astrocytic glial tumors |
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Authors: | B. Frankel Sharon L. Longo Timothy C. Ryken |
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Affiliation: | (1) Molecular Neurosurgery Laboratory, Department of Neurosurgery, SUNY Health Science Center at Syracuse, 750 East Adams St., Rm. 3118 Wsk. Hall, Syracuse, NY 13210, USA Tel.: +1-315-464-5556, Fax: +1-315-464-5504, US;(2) Division of Neurosurgery, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA, US |
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Abstract: | The study of Fas (APO-1/CD95) and Fas ligand (FasL) expression in human glial neoplasms has been primarily restricted to astrocytomas. Using immunohistochemistry, we analyzed 35 non-astrocytic glial neoplasms (12 WHO grade II ependymomas, 15 grade II oligodendrogliomas, and 8 grade III oligodendrogliomas) for these factors. A significant correlation was found between Fas and FasL expression within the same tumors (P = 0.001). Western blotting was used to corroborate these findings in 7 of these tumors (3 ependymomas and 4 oligodendrogliomas). Theoretically, the co-expression of Fas and FasL should render gliomas susceptible to suicidal and fratricidal elimination. Their progressive nature, however, suggests that gliomas have acquired mechanisms to prevent Fas-mediated apoptosis. Expression of the anti-apoptotic protooncogene bcl-2 is one potential way in which Fas/FasL-bearing gliomas can escape this fate. Although expression of Bcl-2 protein was found in 6 of 12 (50%) grade II ependymomas, 5 of 15 (33%) grade II oligodendrogliomas, and 6 of 8 (75%) grade III oligodendrogliomas, no correlation between Fas/FasL co-expression and Bcl-2 production could be demonstrated, indicating that protection from Fas-mediated apoptosis probably involves other mechanisms. Received: 10 November 1998 / Revised: 15 March 1999 / Accepted: 24 March 1999 |
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Keywords: | Fas Fas ligand Bcl-2 Ependymoma Oligodendroglioma |
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