Pc 4 photodynamic therapy of U87-derived human glioma in the nude rat

被引:27
作者
George, JE
Ahmad, Y
Varghai, D
Li, XL
Berlin, J
Jackowe, D
Jungermann, M
Wolfe, MS
Lilge, L
Totonchi, A
Morris, RL
Peterson, A
Lust, WD
Kenney, ME
Hoppel, CL
Sun, JY
Oleinick, NL
Dean, D
机构
[1] Case Western Reserve Univ, Dept Neurol Surg, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Surg, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Anat, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Dept Chem, Cleveland, OH 44106 USA
[6] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[7] Case Western Reserve Univ, Dept Radiat Oncol, Cleveland, OH 44106 USA
[8] Case Western Reserve Univ, Dept Stat, Cleveland, OH 44106 USA
关键词
athymic; cancer; glioblastoma multiforme; photosensitizer; phthalocyanine; mass spectrometry; brain tumor; biophotonics;
D O I
10.1002/lsm.20185
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background and Objectives: As a potential therapy for malignant glioma, we tested the phthalocyanine photosensitizer Pc 4 for: (1) rapid clearance from the vasculature, (2) specificity for glioma, and (3) tumoricidal photosensitizing capability. Study Design/Materials and Methods: Parenchymal injection of U87 cells into athymic rat brains (N = 100) was followed after 12 days by tail vein injection of 0.5 mg/kg Pc 4. After 1 day, the tumor was illuminated with either 5 (N = 11) or 30 (N = 16) J/cm(2) red light at 672 nm. Sacrifice was 1 day later. The brains from these 27 animals underwent H&E (necrosis) and TUNEL assay (apoptosis) histology. Pc 4 concentration of explanted brains and tumors (N = 16), and all blood samples (N = 52) were determined by HPLC-MS 1 day post Pc 4 administration. Results: Tumor-specific apoptosis was almost uniformly seen; however, necrosis was found mostly in the high-light-dose group. Pc 4 concentration in bulk tumor averaged 3.8 times greater than in normal brain. Conclusions: These results warrant expanding this preclinical study to seek effective baseline Pc 4 drug- and light-doses and infusion-to-photoirradiation timing that would be necessary for a Pc 4-mediated PDT clinical trial for glioma patients. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:383 / 389
页数:7
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