A camptothecin prodrug induces mitochondria-mediated apoptosis in cancer cells with cascade activations.
Xiangjie LuoXiaoqin ChiYaying LinZhaoxuan YangHongyu LinJinhao GaoPublished in: Chemical communications (Cambridge, England) (2021)
Mitochondria are crucial regulators of the intrinsic pathway of apoptosis. Herein, we report a photosensitizer-conjugated camptothecin (CPT)-based prodrug for combinative chemo-photodynamic treatment of solid tumors with cascade activations. Upon light irradiation, our prodrug can effectively target the mitochondria of cancer cells, generate singlet oxygen to increase the level of reactive oxygen species (ROS) and trigger ROS-responsive release of CPT, which synergistically induce mitochondrial damage and cause the apoptosis of cancer cells, therefore achieving high therapeutic efficacy for solid tumors and minimized adverse effects to normal tissues. Our prodrug holds great promise as a potent and inspiring means for cancer treatment.
Keyphrases
- reactive oxygen species
- cancer therapy
- cell death
- oxidative stress
- drug delivery
- photodynamic therapy
- cell cycle arrest
- endoplasmic reticulum stress
- drug release
- dna damage
- endoplasmic reticulum
- transcription factor
- gene expression
- cell proliferation
- squamous cell carcinoma
- combination therapy
- locally advanced
- pi k akt