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GJIC Enhances the phototoxicity of photofrin‐mediated photodynamic treatment by the mechanisms related with ROS and Calcium pathways
Authors:Dengpan Wu  Lixia Fan  Chengfang Xu  Zhen Liu  Yuan Zhang  Lucy Liu  Qin Wang  Liang Tao
Affiliation:1. Department of Pharmacology, Pharmacy School of Xuzhou Medical College, Xuzhou, P.R. China;2. Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Pharmacy School of Xuzhou Medical College, Xuzhou, P.R. China;3. Department of Pharmacology, Zhongshan School of Medicine, Sun Yat‐Sen University, Guangzhou, P.R. China;4. Department of Gynaecology and Obstetrics, the Third Affiliated Hospital of Sun Yat‐Sen University, Guangzhou, P.R. China;5. Department of Cell & Systems Biology, University of Toronto, Ontario, Canada;6. +8620 87335468+8620 87332318
Abstract:Despite initially positive responses, recurrences after Photodynamic treatment (PDT) can occur and there is need for improvement in the effectiveness of PDT. Our study uniquely showed that there was a significantly gap junctional intercellular communication (GJIC)‐dependent PDT cytotoxicity. The presence of GJIC composed of Connexin 32 increased the PDT phototoxicity in transfected HeLa cells and in the xenograft tumors, and the enhanced phototoxicity of Photofrin‐mediated PDT by GJIC was related with ROS and calcium pathways. Our study indicates the possibility that up‐regulation or maintenance of gap junction functionality may be used to increase the efficacy of PDT.
figure

The phototoxicity effect of Photofrin was substantially greater in Dox‐treated cells, which expressed the Cx32 and formed the GJ, than Dox‐untreated.

Keywords:photodynamic treatment  photofrin  gap junction intercellular communication  reactive oxygen species  calcium  hela cell line
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