Evidence map›Paper›PMID 42609363›Full record

ReviewFrontiers in neuroscience2026

Targeting the nuclear factor kappa B pathway for the medical management of intervertebral disc degeneration.

Jiansen Wang, Kaixu Han, Dongfeng Li, Yukang Qin, Jing Zhang, Zhinan Ren, Lei Yu, Guangduo Zhu, Cheng Peng, Yingjie Hao

Abstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Jiansen WangDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Kaixu HanDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Dongfeng LiDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Yukang QinDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Jing ZhangDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Zhinan RenDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Lei YuDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Guangduo ZhuDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Cheng PengDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Yingjie HaoDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc degeneration (IVDD), a key contributor to low back pain, is driven by multiple predisposing factors, such as oxidative stress, inflammation, and mechanical stress, among others, severely impacting patients' quality of life. The nuclear factor kappa B (NF-κB) signaling pathway is crucial in the development of IVDD. This review examines the mechanisms of NF-κB activation, focusing on classical and non-classical pathways and their roles in IVDD progression. A variety of therapeutic approaches have been developed to target the NF-κB pathway, including NSAIDs, proteins, non-coding RNAs, hormones, natural chemicals, and sophisticated biomaterials. These interventions inhibit NF-κB activation, alleviating apoptosis, extracellular matrix (ECM) imbalance, and inflammation in the nucleus pulposus. In this review, we not only focus on summarizing the emerging biomaterials and natural medicines targeting NF-κB to treat IVDD in recent years, but also discuss the current challenges, such as limited drug delivery to the avascular disc and the need to elucidate non-classical NF-κB pathways, and outline future directions for clinical translation. These insights inject new vitality into the treatment of IVDD. Despite progress in targeting NF-κB, significant challenges remain in translating these therapies into clinical practice. Further exploring the potential of targeting the NF-κB pathway in the treatment of IVDD can promote the development of new IVDD treatments.

Indexed as

IVDDmedical managementnatural compoundsNF-κB pathwaynovel materials

Identifiers

PMID42609363
PMCPMC13478109

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.