The Role of Regulated Programmed Cell Death in Osteoarthritis: From Pathogenesis to Therapy

被引:52
作者
Liu, Suqing [1 ,2 ]
Pan, Yurong [1 ,2 ]
Li, Ting [1 ,3 ]
Zou, Mi [1 ,3 ]
Liu, Wenji [1 ,3 ]
Li, Qingqing [1 ,3 ]
Wan, Huan [1 ,3 ]
Peng, Jie [3 ]
Hao, Liang [1 ]
机构
[1] Nanchang Univ, Affifiliated Hosp 2, Dept Orthoped, Nanchang 330006, Peoples R China
[2] Nanchang Univ, Queen Marry Coll, Nanchang 330006, Peoples R China
[3] Nanchang Univ, Clin Med Coll 2, Nanchang 330006, Peoples R China
基金
中国国家自然科学基金; 英国科研创新办公室;
关键词
programmed cell death; osteoarthritis; pathogenesis; therapy; NF-KAPPA-B; HYPOXIA-INDUCIBLE FACTOR-2-ALPHA; STRESS-INDUCED APOPTOSIS; CHONDROCYTE APOPTOSIS; NITRIC-OXIDE; ER STRESS; MATRIX METALLOPROTEINASES; CARTILAGE DEGENERATION; KNEE OSTEOARTHRITIS; ARTICULAR-CARTILAGE;
D O I
10.3390/ijms24065364
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
Osteoarthritis (OA) is a worldwide chronic disease that can cause severe inflammation to damage the surrounding tissue and cartilage. There are many different factors that can lead to osteoarthritis, but abnormally progressed programmed cell death is one of the most important risk factors that can induce osteoarthritis. Prior studies have demonstrated that programmed cell death, including apoptosis, pyroptosis, necroptosis, ferroptosis, autophagy, and cuproptosis, has a great connection with osteoarthritis. In this paper, we review the role of different types of programmed cell death in the generation and development of OA and how the different signal pathways modulate the different cell death to regulate the development of OA. Additionally, this review provides new insights into the radical treatment of osteoarthritis rather than conservative treatment, such as anti-inflammation drugs or surgical operation.
引用
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页数:22
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