Hematoporphyrin derivative-mediated photodynamic therapy for human nasopharyngeal carcinoma: a comparative study with CNE2 and C666-1 cell lines in vitro.
- Author:
Xiao-Min YANG
1
;
Rong-Cheng LUO
;
Hong-Jing MA
;
Li-Bo LI
;
Xue-Mei DING
;
Xiao YAN
;
Cheng-Wei LÜ
;
Xiao-Ping ZHOU
Author Information
- Publication Type:Journal Article
- MeSH: Antineoplastic Agents; pharmacology; Cell Line, Tumor; Cell Survival; drug effects; radiation effects; Dose-Response Relationship, Drug; Dose-Response Relationship, Radiation; Hematoporphyrin Derivative; pharmacology; Hematoporphyrin Photoradiation; methods; Humans; Nasopharyngeal Neoplasms; pathology; Photochemotherapy; methods; Photosensitizing Agents; pharmacology
- From: Journal of Southern Medical University 2007;27(2):165-167
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate biological effect of hematoporphyrin derivative (HpD) photodynamic therapy (PDT) on in vitro cultured nasopharyngeal carcinoma (NPC) cell lines CNE2 and C666-1.
METHODSCNE2 and C666-1 cells cultured in vitro were incubated in a medium containing HpD at different concentrations (0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, and 4.0 microg/ml) for 4 h followed by exposure to different light doses (2, 5, 10, and 20 J/cm2) using a diode laser at 630 nm with power density of 20 mW/cm2. After 24 h of incubation with HpD-PDT, the survival rate of CNE2 and C666-1 cells were analyzed by MTT assay.
RESULTSHpD-PDT produced effective killing of CNE2 and C666-1 cells cultured in vitro, and the killing effects were positively correlated with HpD concentration and the irradiation dose. Exposure of CNE2 and C666-1 cells to irradiation dose of 20 J/cm2 resulted in the IC50 of 0.7 and 1.2 microg/ml, respectively (P<0.01). With the same HpD concentration and irradiation dose, the survival rate of C666-1 cells, however, was significantly higher than that of CNE2 cells (P<0.05).
CONCLUSIONHpD-PDT may result in effective killing of CNE2 and C666-1 cells cultured in vitro, although C666-1 cells are less sensitive to HpD-PDT than CNE2 cells.