Dysregulation of mitophagy and mitochondrial homeostasis in cancer stem cells: Novel mechanism for anti-cancer stem cell-targeted cancer therapy

被引:21
|
作者
Praharaj, Prakash Priyadarshi [1 ]
Patro, Birija Sankar [2 ]
Bhutia, Sujit Kumar [1 ]
机构
[1] Natl Inst Technol Rourkela, Dept Life Sci, Canc & Cell Death Lab, Rourkela 769008, Odisha, India
[2] Bhabha Atom Res Ctr, Bioorgan Div, Mumbai, Maharashtra, India
关键词
biogenesis; cancer stem cells; mitochondrial fission; mitochondrial fusion; mitochondrial retrograde response; oxidative phosphorylation; targeted cancer therapy; EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER; OXIDATIVE-PHOSPHORYLATION; CONCISE GUIDE; PROTEOLYTIC CLEAVAGE; SIDE POPULATION; DRUG-RESISTANCE; MEMBRANE-FUSION; OVARIAN-CANCER; DYNAMICS;
D O I
10.1111/bph.15401
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the potential of cancer medicine, cancer stem cells (CSCs) associated with chemoresistance and disease recurrence are the significant challenges currently opposing the efficacy of available cancer treatment options. Mitochondrial dynamics involving the fission-fusion cycle and mitophagy are the major contributing factors to better adaptation, enabling CSCs to survive and grow better under tumour micro-environment-associated stress. Moreover, mitophagy is balanced with mitochondrial biogenesis to maintain mitochondrial homeostasis in CSCs, which are necessary for the growth and maintenance of CSCs and regulate metabolic switching from glycolysis to oxidative phosphorylation. In this review, we discuss different aspects of mitochondrial dynamics, mitophagy, and mitochondrial homeostasis and their effects on modulating CSCs behaviour during cancer development. Moreover, the efficacy of pharmacological targeting of these cellular processes using anti-CSC drugs in combination with currently available chemotherapeutic drugs improves the patient's survival of aggressive cancer types.
引用
收藏
页码:5015 / 5035
页数:21
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