Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY
Volume 73, Issue 1-2, Pages 35-42Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotobiol.2003.09.009
Keywords
5-ALA; lung; photodynamic; tumour invasion; fluorescence
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5-ALA-induced protoporphyrin IX (PPIX) fluorescence kinetics was quantified by fluorescence microscopy in three-dimensional organ co-cultures of human bronchial epithelium, which were infiltrated by four different lung tumour cell lines (EPLC-M31, LCLC-103H, NCI-H125 and NCI-H841). Corresponding fluorescence measurements were performed in monolayer cultures of these tumour cell lines and BEAS-2B cells as a model for normal bronchial epithelium by flow cytometry. Significant differences of fluorescence intensities (FI) between the tumours were detected in organ co-cultures as well as in single cell measurements. Relative FI values in organ co-cultures (FIEPLC-32M1 > FILCLC-H103 > FINCI-H125 > FINCI-H841) did not correspond to the measurements in single cells (FILCLGH103 > FINCI-H125 > FINCI-H841 > FIEPLC-32M1). Histology of organ co-cultures revealed different patterns of invasion and tumour cell densities depending on the tumour type. After correction of Fi in the co-cultures to tumour cell density the correlation coefficient for fluorescence values between both models increased considerably. Thus, additionally to distinctive features of 5-ALA metabolism, patterns of tumour invasion may be a factor determining 5-ALA-induced fluorescence. Considering these results, a pronounced heterogeneity of 5-ALA-induced fluorescence might be expected in different bronchial tumours in vivo. This could interfere with the diagnostic reliability of 5-ALA-induced fluorescence for early tumour detection. (C) 2003 Elsevier B.V. All rights reserved.
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