Cyclooxygenase-2 is a possible target of treatment approach in conjunction with photodynamic therapy for various disorders in skin and oral cavity

被引:39
作者
Akita, Y
Kozaki, K [1 ]
Nakagawa, A
Saito, T
Ito, S
Tamada, Y
Fujiwara, S
Nishikawa, N
Uchida, K
Yoshikawa, K
Noguchi, T
Miyaishi, O
Shimozato, K
Saga, S
Matsumoto, Y
机构
[1] Aichi Med Univ, Sch Med, Dept Pathol, Aichi 4801195, Japan
[2] Aichi Med Univ, Sch Med, Dept Dermatol, Aichi 4801195, Japan
[3] Aichi Gakuin Univ, Sch Dent, Dept Oral & Maxillofacial Surg 2, Chikusa Ku, Aichi 4648650, Japan
[4] Aichi Gakuin Univ, Sch Dent, Dept Periodontol, Chikusa Ku, Aichi 4648650, Japan
关键词
COX-2; inhibitor; cyclooxygenase-2; oral mucosa; photodynamic therapy; skin;
D O I
10.1111/j.1365-2133.2004.06053.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Anti-cancer effects of cyclooxygenase (COX)-2 inhibitors have been reported, but not fully investigated in skin and oral diseases. 5-aminolaevulinic acid (ALA)-based photodynamic therapy (PDT) for treating those patients with skin and oral lesions is a highly sophisticated procedure, but the incidence of disease recurrence after treatment is rather significant. Objective To confirm that COX-2 could be a molecular target in adjunctive therapy to ALA-based PDT, we investigated (i) COX-2 expression in various skin and oral diseases, and (ii) the inhibitory effects on cellular growth of COX-2 selective inhibitor (nimesulide), ALA-based PDT and their combination on human oral squamous cell carcinoma (SCC) cell lines. Methods A total of 129 biopsy samples from the skin and oral mucosal lesions were tested immunohistochemically for COX-2 expression. Then the in vitro effects of nimesulide, ALA-based PDT, and their combination were determined on two SCC cell lines, HSC-2 and HSC-4. Three different methods (MTT assay, double-staining for annexin V and propidium iodide, caspase-3/CPP32 fluorometric protease assay) were applied for evaluation of their inhibitory effects on these two cell lines. Results Among the skin diseases, a considerable number of COX-2 high expressers were found in actinic keratosis (15 of 25, 60%), Bowen's disease (13 of 17, 76%) and extramammary Paget's disease (15 of 15, 100%). In contrast, only one of 33 (3%) basal cell carcinoma tumours was a COX-2 high expresser. Among the oral mucosal biopsies, the proportion of COX-2 high expressers increased gradually from hyperplasia (one of six, 17%) through mild dysplasia (five of eight, 63%) and moderate dysplasia (20 of 23, 87%) to severe dysplasia (two of two, 100%). Nimesulide had an inhibitory effect in vitro on HSC-2 (proven to be a COX-2 high expresser), but not on HSC-4 (a COX-2 non-expresser). While ALA-based PDT showed an inhibitory effect on both HSC-2 and HSC-4, most importantly the combination of nimesulide and ALA-based PDT demonstrated a significant synergistic effect on the cellular growth inhibition of only HSC-2, but not of HSC-4. Conclusions Our study strongly suggests that COX-2 can be one of the molecular targets in treating various skin and oral diseases. The results from our in vitro experiments also prompt us to develop a new protocol with a combination of COX-2 selective inhibitor and ALA-based PDT for more effective treatment of those diseases.
引用
收藏
页码:472 / 480
页数:9
相关论文
共 37 条
[21]   Inhibition of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced mouse lung tumor formation by FGN-1 (sulindac sulfone) [J].
Malkinson, AM ;
Koski, KM ;
Dwyer-Nieldl, LD ;
Rice, PL ;
Rioux, N ;
Castonguay, A ;
Ahnen, DJ ;
Thompson, H ;
Pamukcu, R ;
Piazza, GA .
CARCINOGENESIS, 1998, 19 (08) :1353-1356
[22]   Differential apoptotic pattern induced by photodynamic therapy and cisplatin in human squamous cell carcinoma cell line [J].
Matsumoto, Y ;
Muro, Y ;
Banno, S ;
Ohashi, M ;
Tamada, Y .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1996, 289 (01) :52-54
[23]  
Morton CA, 2001, ARCH DERMATOL, V137, P319
[24]   Histological changes and involvement of apoptosis after photodynamic therapy for actinic keratoses [J].
Nakaseko, H ;
Kobayashi, M ;
Akita, Y ;
Tamada, Y ;
Matsumoto, Y .
BRITISH JOURNAL OF DERMATOLOGY, 2003, 148 (01) :122-127
[25]   Apoptosis and necrosis induced with light and 5-aminolaevulinic acid-derived protoporphyrin IX [J].
Noodt, BB ;
Berg, K ;
Stokke, T ;
Peng, Q ;
Nesland, JM .
BRITISH JOURNAL OF CANCER, 1996, 74 (01) :22-29
[26]   Celecoxib, a cyclooxygenase 2 inhibitor as a potential chemopreventive to UV-induced skin cancer - A study in the hairless mouse model [J].
Orengo, IF ;
Gerguis, J ;
Phillips, R ;
Guevara, A ;
Lewis, AT ;
Black, HS .
ARCHIVES OF DERMATOLOGY, 2002, 138 (06) :751-755
[27]  
Oshima M, 2001, CANCER RES, V61, P1733
[28]   Expression of cyclo-oxygenase-2 in human tongue carcinoma and its precursor lesions [J].
Renkonen, J ;
Wolff, H ;
Paavonen, T .
VIRCHOWS ARCHIV, 2002, 440 (06) :594-597
[29]   Photodynamic therapy for the treatment of extramammary Paget's disease [J].
Shieh, S ;
Dee, AS ;
Cheney, RT ;
Frawley, NP ;
Zeitouni, NC ;
Oseroff, AR .
BRITISH JOURNAL OF DERMATOLOGY, 2002, 146 (06) :1000-1005
[30]   Cyclooxygenase-2 inhibitors in tumorigenesis (Part II) [J].
Taketo, MM .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (21) :1609-1620