Synthesis,and biological evaluation of 2-(4-aminophenyl)benzothiazole derivatives as photosensitizing agents |
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Authors: | Wan-Ping Hu Yin-Kai Chen Chao-Cheng Liao Hsin-Su Yu Yi-Min Tsai Shu-Mei Huang Feng-Yuan Tsai Ho-Chuan Shen Long-Sen Chang Jeh-Jeng Wang |
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Affiliation: | 1. Department of Biotechnology, College of Life Science, Kaohsiung Medical University, Kaohsiung, Taiwan;2. Department of Dermatology, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;3. Center of Excellence for Environmental Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;4. Division of Environmental Health and Occupational Medicine, National Health Research Institutes, Miaoli, Taiwan;5. Institute of Biomedical Science, National Sun Yat-Sen University, Kaohsiung, Taiwan;6. Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung City 807, Taiwan |
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Abstract: | Photodynamic therapy (PDT) employing exogenous photosensitizers is currently being approved for treatment of basal cell carcinoma (BCC). 2-(4-Aminophenyl)benzothiazoles (6) consist of chromophoric structure and absorb light in the UVA (315–400 nm). These results encouraged us to design and synthesize a diversity of 2-phenylbenzothiazoles (6). Studies on the apoptotic mechanism involved in photosensitive effects induced by UVA-activated 6 in BCC cells are carried out in the present article. 6-UVA-treated cells displayed several features of apoptosis, including an increase in the sub-G1 population, a significantly increased annexin V binding, and activation of caspase-3. 6-UVA induced a decrease in mitochondrial membrane potential (Δψmt) and ATP via enhanced ROS generation and promoted phosphorylation of extracellular signal-regulated kinase (ERK) and p38 MAPK expression. These results suggest that 6-UVA elicits photosensitive effects in mitochondria processes which involve ERK and p38 activation, and ultimately lead to BCC cell apoptosis. |
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