A Review of Advances in Mitochondrial Research in Cancer

被引:2
作者
Li, Zhiru [1 ,2 ]
Zhang, Wu [3 ]
Guo, Shaowei [2 ]
Qi, Guoyan [3 ]
Huang, Jiandi [2 ,4 ]
Gao, Jin [5 ]
Zhao, Jing [6 ]
Kang, Lin [7 ]
Li, Qingxia [2 ]
机构
[1] North China Univ Sci & Technol, Grad Sch, Tangshan, Peoples R China
[2] Hebei Gen Hosp, Dept Oncol 4, Shijiazhuang, Peoples R China
[3] Hebei Med, Peoples Hosp Shijiazhuang, Ctr Treatment Myasthenia Gravis, Shijiazhuang, Peoples R China
[4] Hebei North Univ, Grad Sch, Zhangjiakou, Peoples R China
[5] Hebei Gen Hosp, Dept Thyroid & Breast Surg Ward, Shijiazhuang, Peoples R China
[6] Hebei Gen Hosp, Dept Oncol 6, Shijiazhuang, Peoples R China
[7] Hebei Gen Hosp, Dept Pathol, Shijiazhuang, Peoples R China
关键词
cancer; mitochondrial dysfunction; metabolic reprogramming; mitochondria-targeting; immune microenvironment; DNA MUTATIONS; AEROBIC GLYCOLYSIS; OXIDATIVE-PHOSPHORYLATION; TUMOR MICROENVIRONMENT; METABOLIC REQUIREMENTS; STROMAL CELLS; DYNAMICS; BREAST; PROGRESSION; TRANSPORT;
D O I
10.1177/10732748241299072
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAbnormalities in mitochondrial structure or function are closely related to the development of malignant tumors. Mitochondrial metabolic reprogramming provides precursor substances and energy for the vital activities of tumor cells, so that cancer cells can rapidly adapt to the unfavorable environment of hypoxia and nutrient deficiency. Mitochondria can enable tumor cells to gain the ability to proliferate, escape immune responses, and develop drug resistance by altering constitutive junctions, oxidative phosphorylation, oxidative stress, and mitochondrial subcellular relocalization. This greatly reduces the rate of effective clinical control of tumors.PurposeExplore the major role of mitochondria in cancer, as well as targeted mitochondrial therapies and mitochondria-associated markers.ConclusionsThis review provides a comprehensive analysis of the various aspects of mitochondrial aberrations and addresses drugs that target mitochondrial therapy, providing a basis for clinical mitochondria-targeted anti-tumor therapy.
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页数:13
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