Cell Death Pathways Associated with Photodynamic Therapy: An Update

被引:187
|
作者
Kessel, David [1 ]
Oleinick, Nancy L. [2 ,3 ]
机构
[1] Wayne State Univ, Sch Med, Detroit, MI 48202 USA
[2] Case Western Reserve Univ, Sch Med, Cleveland, OH USA
[3] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH USA
关键词
INDUCED APOPTOSIS; CYTOCHROME-C; LYSOSOMAL PHOTODAMAGE; ENDOPLASMIC-RETICULUM; PROAPOPTOTIC SIGNALS; PROSTATE-CANCER; AUTOPHAGY; BCL-2; EFFICACY; PHOTOSENSITIZER;
D O I
10.1111/php.12857
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
Photodynamic therapy (PDT) has the potential to make a significant impact on cancer treatment. PDT can sensitize malignant tissues to light, leading to a highly selective effect if an appropriate light dose can be delivered. Variations in light distribution and drug delivery, along with impaired efficacy in hypoxic regions, can reduce the overall tumor response. There is also evidence that malignant cells surviving PDT may become more aggressive than the initial tumor population. Promotion of more effective direct tumor eradication is therefore an important goal. While a list of properties for the ideal photosensitizing agent often includes formulation, pharmacologic and photophysical elements, we propose that subcellular targeting is also an important consideration. Perspectives relating to optimizing PDT efficacy are offered here. These relate to death pathways initiated by photodamage to particular subcellular organelles.
引用
收藏
页码:213 / 218
页数:6
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