Photochemical activation of drugs for the treatment of therapy-resistant cancers

被引:27
作者
Weyergang, Anette [1 ]
Berstad, Maria E. B. [1 ]
Bull-Hansen, Bente [1 ]
Olsen, Cathrine E. [1 ,2 ]
Selbo, Pal K. [1 ,2 ]
Berg, Kristian [1 ]
机构
[1] Oslo Univ Hosp, Norwegian Radium Hosp, Inst Canc Res, Dept Radiat Biol, Montebello, Norway
[2] Oslo Univ Hosp, Norwegian Radium Hosp, Inst Canc Res, Canc Stem Cell Innovat Ctr SFI CAST, Oslo, Norway
关键词
GROWTH-FACTOR RECEPTOR; PHOTODYNAMIC THERAPY; ACQUIRED-RESISTANCE; INTERNALIZATION; MECHANISMS; DELIVERY; CELLS; EGFR; CYTOTOXICITY; DOXORUBICIN;
D O I
10.1039/c5pp00029g
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
Resistance to chemotherapy, molecular targeted therapy as well as radiation therapy is a major obstacle for cancer treatment. Cancer resistance may be exerted through multiple different mechanisms which may be orchestrated as observed in multidrug resistance (MDR). Cancer resistance may be intrinsic or acquired and often leaves patients without any treatment options. Strategies for alternative treatment modalities for resistant cancer are therefore highly warranted. Photochemical internalization (PCI) is a technology for cytosolic delivery of macromolecular therapeutics based on the principles of photodynamic therapy (PDT). The present report reviews the current knowledge of PCI of therapy-resistant cancers. In summary, PCI may be able to circumvent several of the major mechanisms associated with resistance towards chemotherapeutics including increased expression of drug efflux pumps, altered intracellular drug distribution and increased ROS scavenging. Current data also suggest PCI of targeted toxins as highly effective in cancers resistant to clinically available targeted therapy such as monoclonal antibodies (mAbs) and tyrosine kinase inhibitors (TKIs). PCI may therefore, in general, represent a future treatment option for cancers resistant to other therapies.
引用
收藏
页码:1465 / 1475
页数:11
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