Topical methotrexate pretreatment enhances the therapeutic effect of topical 5-aminolevulinic acid-mediated photodynamic therapy on hamster buccal pouch precancers

被引:10
作者
Yang, Deng-Fu [1 ]
Lee, Jeng-Woei [2 ]
Chen, Hsin-Ming [3 ,4 ]
Hsu, Yih-Chih [1 ,5 ,6 ]
机构
[1] Chung Yuan Christian Univ, Dept Biosci Technol, Taoyuan 32023, Taiwan
[2] Tzu Chi Univ, Dept Life Sci, Hualien, Taiwan
[3] Natl Taiwan Univ, Sch Dent, Grad Inst Oral Biol, Taipei 10764, Taiwan
[4] Natl Taiwan Univ Hosp, Coll Med, Dept Dent, Taipei, Taiwan
[5] Chung Yuan Christian Univ, Ctr Nanotechnol, Taoyuan, Taiwan
[6] Chung Yuan Christian Univ, Ctr Biomed Technol, Taoyuan, Taiwan
关键词
5-aminolevulinic acid; hamster buccal pouch precancer; methotrexate; oral precancerous Lesions; topical photodynamic therapy; ORAL VERRUCOUS HYPERPLASIA; AMINOLEVULINIC-ACID; LESIONS; AUTOFLUORESCENCE; ACCUMULATION; CRYOTHERAPY; CARCINOMA; CANCER; CELLS; ALA;
D O I
10.1016/j.jfma.2014.03.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Purpose: Topical 5-aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) is effective for treatment of human oral precancerous lesions. This animal study aimed to assess whether topical methotrexate (MTX) pretreatment could enhance the therapeutic effect of topical ALA-PDT on hamster buccal pouch precancerous lesions. Methods: Twenty hamster buccal pouch precancerous lesions were treated with either topical ALA-PDT with topical MTX pretreatment (topical MTX-ALA-PDT group, n = 10) or topical ALA-PDT alone (topical ALA-PDT group, n = 10). The intracellular protoporphyrin IX (PplX) level in another 12 precancerous lesions (n = 6 for either the topical MTX-ALA or topical ALA group) was monitored by fluorescence spectroscopy. Results: The intracellular PpIX reached its peak level in precancerous lesions 6.5 hours and 2.5 hours after topical ALA application for the topical MTX-ALA group (5.63-fold higher in the lesion than in the normal mucosa) and topical ALA group (2.42-fold higher in the lesion than in the normal mucosa), respectively. The complete response rate of precancerous lesions was 80% for the topical MTX-ALA-PDT group and 70% for the topical ALA-PDT group. In addition, the topical MTX-ALA-PDT group required a significantly lower mean treatment number (2.1 +/- 0.6) to achieve complete response than the topical ALA-PDT group (4.4 +/- 1.3, p < 0.001)). Moreover, the topical MTX-ALA-PDT group had a lower recurrence rate (12.5%) than the topical ALA-PDT group (28.6%). Conclusion: We conclude that topical MTX-pretreatment can increase intracellular PpIX production in hamster buccal pouch precancerous lesions and significantly improves the outcomes of the precancerous lesions treated with topical ALA-PDT. Copyright (C) 2014, Elsevier Taiwan LLC Et Formosan Medical Association. All rights reserved.
引用
收藏
页码:591 / 599
页数:9
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