Melanoma resistance to photodynamic therapy: new insights

被引:116
|
作者
Huang, Ying-Ying [1 ,2 ,3 ]
Vecchio, Daniela [1 ,2 ]
Avci, Pinar [1 ]
Yin, Rui [1 ,2 ,4 ]
Garcia-Diaz, Maria [1 ,5 ,6 ]
Hamblin, Michael R. [1 ,2 ,7 ]
机构
[1] Massachusetts Gen Hosp, Wellman Ctr Photomed, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Dermatol, Boston, MA 02115 USA
[3] Guangxi Med Univ, Dept Pathol, Nanning, Guangxi, Peoples R China
[4] Third Mil Med Univ, Southwest Hosp, Dept Dermatol, Chongqing, Peoples R China
[5] Ramon Llull Univ, IQS Sch Engn, Mol Engn Grp, Barcelona, Spain
[6] Univ Barcelona, Dept Biochem & Mol Biol, Barcelona, Spain
[7] Harvard MIT, Div Hlth Sci & Technol, Cambridge, MA USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
antitumor immune response; depigmentation; drug efflux systems; melanoma; melanosomes; photodynamic therapy; photosensitizers; resistance mechanisms; IN-SITU PHOTOIMMUNOTHERAPY; B16 PIGMENTED MELANOMA; METASTATIC MELANOMA; MALIGNANT-MELANOMA; CHLORIN E(6); SKIN; CELLS; HYPERICIN; REPAIR; DNA;
D O I
10.1515/hsz-2012-0228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Melanoma is the most dangerous form of skin cancer, with a steeply rising incidence and a poor prognosis in its advanced stages. Melanoma is highly resistant to traditional chemotherapy and radiotherapy, although modern targeted therapies such as BRAF inhibitors are showing some promise. Photodynamic therapy (PDT, the combination of photosensitizing dyes and visible light) has been tested in the treatment of melanoma with some promising results, but melanoma is generally considered to be resistant to it. Optical interference by the highly-pigmented melanin, the antioxidant effect of melanin, the sequestration of photosensitizers inside melanosomes, defects in apoptotic pathways, and the efflux of photosensitizers by ATP-binding cassette transporters have all been implicated in melanoma resistance to PDT. Approaches to overcoming melanoma resistance to PDT include: the discovery of highly active photosensitizers absorbing in the 700-800-nm near infrared spectral region; interventions that can temporarily reduce the amount or pigmentation of the melanin; compounds that can reverse apoptotic defects or inhibit drug-efflux of photosensitizers; and immunotherapy approaches that can take advantage of the ability of PDT to activate the host immune system against the tumor being treated.
引用
收藏
页码:239 / 250
页数:12
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