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Tumor necrosis factor-α: a key contributor to intervertebral disc degeneration
Author(s) -
Cheng Wang,
Xiaohua Yu,
Yiguo Yan,
Wei Yang,
Shujun Zhang,
YongXiao Xiang,
Jian Zhang,
Wenjun Wang
Publication year - 2016
Publication title -
acta biochimica et biophysica sinica
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmw112
Subject(s) - intervertebral disc , medicine , degeneration (medical) , tumor necrosis factor alpha , autophagy , degenerative disc disease , pathological , inflammation , pathology , signal transduction , necrosis , bioinformatics , apoptosis , cancer research , immunology , microbiology and biotechnology , biology , anatomy , biochemistry , alternative medicine
Intervertebral disc (IVD) degeneration (IDD) is the most common cause leading to low back pain (LBP), which is a highly prevalent, costly, and crippling condition worldwide. Current treatments for IDD are limited to treat the symptoms and do not target the pathophysiology. Tumor necrosis factor-α (TNF-α) is one of the most potent pro-inflammatory cytokines and signals through its receptors TNFR1 and TNFR2. TNF-α is highly expressed in degenerative IVD tissues, and it is deeply involved in multiple pathological processes of disc degeneration, including matrix destruction, inflammatory responses, apoptosis, autophagy, and cell proliferation. Importantly, anti-TNF-α therapy has shown promise for mitigating disc degeneration and relieving LBP. In this review, following a brief description of TNF-α signal transduction, we mainly focus on the expression pattern and roles of TNF-α in IDD, and summarize the emerging progress regarding its inhibition as a promising biological therapeutic approach to disc degeneration and associated LBP. A better understanding will help to develop novel TNF-α-centered therapeutic interventions for degenerative disc disease.

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