Mechanism of Differential Susceptibility of Two (Canine Lung Adenocarcinoma) Cell Lines to 5-Aminolevulinic Acid-Mediated Photodynamic Therapy

被引:2
作者
Osaki, Tomohiro [1 ]
Kunisue, Narumi [2 ]
Ota, Urara [2 ]
Imazato, Hideo [2 ]
Ishii, Takuya [2 ]
Takahashi, Kiwamu [2 ]
Ishizuka, Masahiro [2 ]
Tanaka, Tohru [3 ]
Okamoto, Yoshiharu [1 ]
机构
[1] Tottori Univ, Fac Agr, Joint Dept Vet Clin Med, Tottori 6808553, Japan
[2] SBI Pharmaceut Co Ltd, Tokyo 1066020, Japan
[3] Neopharma Japan Co Ltd, Tokyo 1020071, Japan
关键词
photodynamic therapy; lung adenocarcinoma; tumor; canine carcinoma; NITRIC-OXIDE; PROTOPORPHYRIN IX; CANCER; GLUTATHIONE; SENSITIZERS; ALA; RESISTANCE; EFFICIENCY; CARCINOMA; ROLES;
D O I
10.3390/cancers13164174
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Photodynamic therapy (PDT) is a clinically approved, minimally invasive treatment for malignant tumors. Protoporphyrin IX (PpIX), derived from 5-aminolevulinic acid (5-ALA) as the prodrug, is one of the photosensitizers used in PDT. Recently, we reported a significant difference in response to 5-ALA-mediated PDT treatment in two canine primary lung adenocarcinoma cell lines (sensitive to PDT: HDC cells, resistant to PDT: LuBi cells). This study aimed to examine the difference in cytotoxicity of 5-ALA-mediated PDT in these cells. Although intracellular PpIX levels before irradiation were similar between HDC and LuBi cells, the percentage of ROS-positive cells and apoptotic cells in LuBi cells treated with 5-ALA-mediated PDT was significantly lower than that in HDC cells treated with 5-ALA-mediated PDT. A high dosage of the NO donor, DETA NONOate, significantly increased the cytotoxicity of 5-ALA-mediated PDT against LuBi cells. These results suggest that the sensitivity of 5-ALA-mediated PDT might be correlated with NO.
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页数:13
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