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Proceedings Paper

PDT-induced apoptosis: investigations using two malignant brain tumor models
Author(s): Lothar D. Lilge; Keir Menzies; Stuart K. Bisland; Annie Lin; Brian C. Wilson
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Paper Abstract

PDT included necrosis in brain tissue and an intracranial tumor has been quantified for various photosensitizers, and it has been shown to be dependent on the sub-cellular localization of these photosensitizers. In quantifying non- necrotic biological endpoints, such as PDT induced apoptosis, the expression and translation of apoptosis inhibiting or promoting genes is of considerable importance. We studied the susceptibility of two glioblastoma cell lines to under go apoptotic cell death following photodynamic treatment with either Photofrin or delta-aminolevulinic acid (delta) ALA) in vivo. Murine 9L Gliosarcoma cells or human U87 Glioblastoma cells were implanted into the cortex of rats, and following 12 or 14 days of growth respectively, subjected to either Photofrin-mediated PDT or ALA-mediated PDT. 9L gliosarcoma cells express the phosphatase Tensin homologue (PTEN) tumor suppressor gene while in U87 cells PTEN is mutated. Differences in the Photofrin mediated PDT induced apoptosis were noted between the two different cell lines in vivo, suggesting that Photofrin mediated PDT may be dependent on apoptotic pathways. ALA induced PPIX showed higher selectivity towards 9L than Photofrin mediated PDT. These studies suggests that PDT could be used as an effective treatment for intracranial neoplasm. Endogenous photosensitizers such as ALA could be used to promote apoptosis in tumor cells due to PDT treatment and thereby minimize the extent of necrotic infarction in the surrounding normal brain.

Paper Details

Date Published: 6 June 2002
PDF: 7 pages
Proc. SPIE 4612, Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy XI, (6 June 2002); doi: 10.1117/12.469343
Show Author Affiliations
Lothar D. Lilge, Ontario Cancer Institute/Princess Margaret Hospital and Univ. of Toronto (Canada)
Keir Menzies, Ontario Cancer Institute/Princess Margaret Hospital and Univ. of Toronto (Canada)
Stuart K. Bisland, Ontario Cancer Institute/Princess Margaret Hospital and Univ. of Toronto (Canada)
Annie Lin, Ontario Cancer Institute/Princess Margaret Hospital and Univ. of Toronto (Canada)
Brian C. Wilson, Ontario Cancer Institute/Princess Margaret Hospital and Univ. of Toronto (Canada)


Published in SPIE Proceedings Vol. 4612:
Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy XI
Thomas J. Dougherty, Editor(s)

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