Evidence map›Paper›PMID 36008968›Full record

ReviewBiomolecules2022

Role of Caspase Family in Intervertebral Disc Degeneration and Its Therapeutic Prospects.

Lei Li, Jiale He, Guangzhi Zhang, Haiwei Chen, Zhangbin Luo, Bo Deng, Yuan Zhou, Xuewen Kang

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  7. In Vitro and In Silico Cytotoxic Activity of Isocordoin fromInternational journal of molecular sciences · 2025
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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

8 authors at 2 institutions in 1 country.

Lei LiDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.ORCID 0000-0001-8520-2282
Jiale HeAffiliated Hospital of Xizang Minzu University, Xianyang 712082, China.ORCID 0000-0002-4181-4890
Guangzhi ZhangDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.ORCID 0000-0003-3193-0297
Haiwei ChenDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.ORCID 0000-0002-4095-6328
Zhangbin LuoDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.
Bo DengDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.
Yuan ZhouDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.
Xuewen KangDepartment of Orthopedics, Lanzhou University Second Hospital, Lanzhou 730000, China.
Lanzhou University Second Hospital · CNXizang Minzu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc degeneration (IVDD) is a common musculoskeletal degenerative disease worldwide, of which the main clinical manifestation is low back pain (LBP); approximately, 80% of people suffer from it in their lifetime. Currently, the pathogenesis of IVDD is unclear, and modern treatments can only alleviate its symptoms but cannot inhibit or reverse its progression. However, in recent years, targeted therapy has led to new therapeutic strategies. Cysteine-containing aspartate proteolytic enzymes (caspases) are a family of proteases present in the cytoplasm. They are evolutionarily conserved and are involved in cell growth, differentiation, and apoptotic death of eukaryotic cells. In recent years, it has been confirmed to be involved in the pathogenesis of various diseases, mainly by regulating cell apoptosis and inflammatory response. With continuous research on the pathogenesis and pathological process of IVDD, an increasing number of studies have shown that caspases are closely related to the IVDD process, especially in the intervertebral disc (IVD) cell apoptosis and inflammatory response. Therefore, herein we study the role of caspases in IVDD with respect to the structure of caspases and the related signaling pathways involved. This would help explore the strategy of regulating the activity of the caspases involved and develop caspase inhibitors to prevent and treat IVDD. The aim of this review was to identify the caspases involved in IVDD which could be potential targets for the treatment of IVDD.

Indexed as

Intervertebral DiscIntervertebral Disc DegenerationApoptosisCaspase InhibitorsCaspasesHumansCaspase InhibitorsCaspasesapoptosiscaspaseinflammationinhibitorintervertebral disc degeneration

Identifiers

PMID36008968
PMCPMC9406018
OpenAlexW4289985757

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.