Kimani, Stanley G.; Phillips, James B.; Bruce, James I.; MacRobert, Alexander J. and Golding, Jon P.
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|DOI (Digital Object Identifier) Link:||http://doi.org/10.1111/j.1751-1097.2011.01022.x|
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Photodynamic therapy (PDT) is an increasingly popular anticancer treatment that uses photosensitizer, light, and tissue oxygen to generate cytotoxic reactive oxygen species (ROS) within illuminated cells. Acting to counteract ROS-mediated damage are various cellular antioxidant pathways. In this study, we combined PDT with specific antioxidant inhibitors to potentiate PDT cytotoxicity in MCF-7 cancer cells. We used disulphonated aluminium phthalocyanine photosensitizer plus various combinations of the antioxidant inhibitors: diethyl-dithiocarbamate (DDC, a Cu/Zn-SOD inhibitor), 2-Methoxyestradiol (2-ME, a Mn-SOD inhibitor), L-buthionine sulfoximine (BSO, a glutathione synthesis inhibitor) and 3-amino-1,2,4-Triazole (3-AT, a catalase inhibitor). BSO, singly or in combination with other antioxidant inhibitors, significantly potentiated PDT cytotoxicity, corresponding with increased ROS levels and apoptosis. The greatest potentiation of cell death over PDT alone was seen when cells were pre-incubated for 24 hours with 300 ?M BSO plus 10 mM 3-AT (1.62-fold potentiation) or 300 ?M BSO plus 1 ?M 2-ME (1.52-fold), or with a combination of all four inhibitors (300 ?M BSO, 10 mM 3-AT, 1 ?M 2-ME, 10 ?M DDC: 1.4-fold). Because many of these inhibitors have already been clinically tested, this work facilitates future in vivo studies.
|Item Type:||Journal Article|
|Copyright Holders:||2011 The Authors|
Science > Life, Health and Chemical Sciences
Other Departments > Research, Scholarship and Quality Office
|Interdisciplinary Research Centre:||Biomedical Research Network (BRN)
Centre for Earth, Planetary, Space and Astronomical Research (CEPSAR)
|Depositing User:||Jon Golding|
|Date Deposited:||16 Nov 2011 13:35|
|Last Modified:||29 May 2016 15:10|
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