4.4 Article

Assessment of natural antioxidants' effect on PDT cytotoxicity through fluorescence microscopy image analysis

Journal

LASERS IN SURGERY AND MEDICINE
Volume 54, Issue 2, Pages 311-319

Publisher

WILEY
DOI: 10.1002/lsm.23469

Keywords

antioxidants; photodynamic therapy; polyphenols; prostate cancer

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This study evaluated the enhancement of PDT cytotoxicity by combining it with a rich natural antioxidant mixture from Pinus halepensis bark extract in pro-oxidant concentrations. The results showed that P. halepensis bark extract increased intracellular ROS levels in a concentration-dependent manner, leading to cytotoxic effects on LNCaP prostate cancer cells and potential as an anticancer agent in prostate cancer treatment. Additionally, the combination of P. halepensis bark extract with m-THPC-PDT demonstrated an enhancement in cellular death levels, suggesting its potential as a supplementary agent to improve prostate cancer PDT treatment.
Background and Objectives Photodynamic therapy (PDT) is a cancer treatment modality mediated by reactive oxygen species (ROS). However, the intracellular antioxidant defense system antagonizes PDT-generated ROS, impeding PDT efficacy. This study aimed to evaluate the enhancement of PDT cytotoxicity by its combination with natural antioxidants in pro-oxidant concentrations. Methods A rich natural antioxidant mixture originating from Pinus halepensis bark extract was studied for its potential to enhance the efficacy of m-tetrahydroxyphenylchlorin (m-THPC)-PDT on LNCaP prostate cancer cells, in vitro. Various P. halepensis concentrations, at two different incubation times, were used in combination with m-THPC-PDT. Assessment of cellular viability and intracellular ROS levels evaluated the treatments' outcome. A novel method was developed for the assessment of the intracellular ROS levels, based on image analysis and data extraction from fluorescence microscopy images. Results P. halepensis bark extract increased the intracellular ROS levels in a concentration-dependent but not in an incubation-dependent manner. The higher concentrations used (>= 50 mu g/ml) reduced cellular viability even by 50%. One hour pretreatment with 30 mu g/ml P. halepensis before m-THPC-PDT exceeded the levels of cellular death by approximately 15%. Conclusions The results provided evidence of the cytotoxic effect of P. halepensis bark extract on LNCaP cells, showing the potential of P. halepensis to be used as an anticancer agent in prostate cancer treatment. The results also provided evidence of enhancement of m-THPC-PDT by P. halepensis bark extract showed the potential to be used as a supplementary agent to improve prostate cancer PDT treatment.

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