Heterogeneity of delta-aminolevulinic acid-induced protoporphyrin IX fluorescence in human glioma cells and leukemic lymphocytes

• Published in: Neurological research (New York) Vol. 22; no. 4; pp. 361 - 368
• Main Authors: Eléouet, S, Rousset, N, Carré, J, Vonarx, V, Vilatte, C, Louët, C, Lajat, Y, Patrice, T
• Format: Journal Article
• Language: English
• Published: England 01-06-2000
• Subjects: Adult; Aged; Aged, 80 and over; Aminolevulinic Acid - pharmacokinetics; Biopsy; Brain Neoplasms - metabolism; Brain Neoplasms - pathology; Brain Neoplasms - therapy; Female; Glioblastoma - metabolism; Glioblastoma - pathology; Glioblastoma - therapy; Humans; Kinetics; Leukemia, Lymphocytic, Chronic, B-Cell - metabolism; Leukemia, Lymphocytic, Chronic, B-Cell - pathology; Leukemia, Lymphocytic, Chronic, B-Cell - therapy; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - metabolism; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - therapy; Lymphocytes - metabolism; Male; Microscopy, Confocal; Microscopy, Fluorescence; Middle Aged; Photochemistry; Phototherapy; Protoporphyrins - biosynthesis; Tumor Cells, Cultured - metabolism; Tumor Cells, Cultured - pathology
• ISSN: 0161-6412
• DOI: 10.1080/01616412.2000.11740685

Delta-aminolevulinic acid (ALA)-PDT efficacy is particularly dependent on the quality of protoporphyrin IX (PpIX)-induced synthesis. The purpose of this study was to determine the ability of cells from two human cancer types to synthesise PpIX after ALA administration. Biopsies of glioma cells have been obtained from patients with glioblastomas that have or have not been given ALA IV (ex vivo incubation). Peripheral blood lymphocytes, obtained from leukemic patients, have also been ALA-incubated in vitro. In glioma cells, fluorescence heterogeneity was extensive either in ALA infused patients or in ex vivo ALA incubated cells. Mean intensities after 3 h were 110 cts (range 0-340) and 1000 cts (range 0-3600). Similar results were found in leukemic lymphocytes where cell fluorescence varied from 0 to 480 cts with a percentage of fluorescent cells varying with time and from one patient to another. Furthermore, PpIX was not detectable in two patients with CLL. These observations suggest that a marked heterogeneity of ALA uptake and/or PpIX synthesis exists in a given human cancer cell population particularly after systemic administration. Improvements for ALA transformation into PpIX are strongly recommended to ensure the efficacy of ALA/PpIX-PDT.