1. Photosensitization of cells with different metastatic potentials by liposome-delivered Zn(II)-phthalocyanine
- Author
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Giulio Jori, Spiridione Garbisa, Elena Reddi, and Giuliana Valduga
- Subjects
Radiation-Sensitizing Agents ,Cancer Research ,Cell Membrane Permeability ,Indoles ,Mice, Nude ,Isoindoles ,Mice ,chemistry.chemical_compound ,Adenosine Triphosphate ,Lactate dehydrogenase ,Organometallic Compounds ,Animals ,Neoplasm Metastasis ,Cytotoxicity ,Drug Carriers ,Liposome ,Photosensitizing Agents ,biology ,Chemistry ,Deoxyglucose ,Succinate dehydrogenase ,Cell Membrane ,Biological Transport ,DNA, Neoplasm ,Neoplasms, Experimental ,Rats ,Photochemotherapy ,Oncology ,Biochemistry ,Zinc Compounds ,Cell culture ,Liposomes ,Biophysics ,biology.protein ,Phototoxicity ,Intracellular - Abstract
The phototoxicity of liposome-incorporated Zn(II)-phthalocyanine (ZnPc) and its water-soluble tetrasulphonated derivative (ZnPcTS) was studied in the tumorigenic but nonmetastatic (RE4) and the highly metastatic (4R) transformed rat embryo fibroblasts. Upon irradiation with 585–605 nm light in the presence of ZnPc, the cell survival drastically decreased, while it was unaffected by ZnPcTS. Enzymatic assays showed that ZnPc induced about a 60% decrease in the activity of the mitochondrial enzymes NADH and succinate dehydrogenase after 3 min of irradiation, while no significant reduction in the activity of lactate dehydrogenase and lysosomal N-acetyl-β-glucosaminidase was observed. The transport of thymidine, deoxyglucose and α-aminoisobutyric acid through the plasma membrane was strongly inhibited after irradiation. Similarly, the intracellular ATP content was significantly reduced. The reduction of DNA biosynthesis showed a time dependence quite similar to the photo-induced decrease in cell survival. No repair of cellular functions affected by ZnPc was observed in the 2 cell lines. These results indicate that, under our experimental conditions, hydrophobic ZnPc exerts its cytotoxic activity mainly by impairing those functions localized in the plasma membrane of the cells. Int. J. Cancer 75:412–417, 1998. © 1998 Wiley-Liss, Inc.
- Published
- 1998
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