Evidence map›Paper›PMID 40624664›Full record

ArticleJournal of nanobiotechnology2025

Quercetin nanoformulation-embedded hydrogel inhibits osteopontin mediated ferroptosis for intervertebral disc degeneration alleviation.

Jitian Li, Lemeng Ren, Lei Wan, Man Liu, Mingyu Zhao, Yazhou Lin, Jiancheng Zheng, Yun Tang, Yage Luo, Yan Ma and 5 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. [Research progress of hydrogel-based growth factors for treatment of intervertebral disc degeneration].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2025
    Review
  8. Article
  9. Review
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

15 authors.

Jitian Li *The Third Affiliated Hospital of Xinxiang Medical University, Clinical Medical Center of Tissue Engineering and Regeneration, Zhongyuan Regenerative Medicine Laboratory, Xinxiang Medical University, Xinxiang, 453000, China.
Lemeng Ren *Department of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China.
Lei Wan *Department of Osteology, The Second Affiliated Hospital of Luohe Medical College, Luohe, 462300, China.
Man LiuLaboratory of Molecular Biology, Luoyang Orthopedic Hospital of Henan Province (Orthopedic Hospital of Henan Province), Henan University of Chinese Medicine, Zhengzhou, 450000, China.
Mingyu ZhaoLaboratory of Molecular Biology, Luoyang Orthopedic Hospital of Henan Province (Orthopedic Hospital of Henan Province), Henan University of Chinese Medicine, Zhengzhou, 450000, China.
Yazhou LinDepartment of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China.
Jiancheng ZhengDepartment of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China.
Yun TangDepartment of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China.
Yage LuoLaboratory of Molecular Biology, Luoyang Orthopedic Hospital of Henan Province (Orthopedic Hospital of Henan Province), Henan University of Chinese Medicine, Zhengzhou, 450000, China.
Yan MaLaboratory of Molecular Biology, Luoyang Orthopedic Hospital of Henan Province (Orthopedic Hospital of Henan Province), Henan University of Chinese Medicine, Zhengzhou, 450000, China.
Lei WangThe Third Affiliated Hospital of Xinxiang Medical University, Clinical Medical Center of Tissue Engineering and Regeneration, Zhongyuan Regenerative Medicine Laboratory, Xinxiang Medical University, Xinxiang, 453000, China.
Peng CaoDepartment of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China.
Zhe ChenDepartment of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China. drchenzhe@live.com.ORCID http://orcid.org/0000-0002-9721-5301
Wenjie RenThe Third Affiliated Hospital of Xinxiang Medical University, Clinical Medical Center of Tissue Engineering and Regeneration, Zhongyuan Regenerative Medicine Laboratory, Xinxiang Medical University, Xinxiang, 453000, China. wjren1966@163.com.ORCID http://orcid.org/0000-0003-4711-2352
Fei WangDepartment of Orthopedics, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China. wangfeirj@163.com.ORCID http://orcid.org/0009-0009-4730-8591

Funding

Key Research and Development Project in Henan Province 231111310500National Key Research and Development Program of China 2023YFC2508806National Natural Science fund of China 82474554Scientific Research Project of Henan Zhongyuan Medical Science and Technology Innovation and Development Foundation ZYYC2023ZDthe Shanghai Bureau of Health 20214Y0132
6 · The paper itself

Abstract

Reactive oxygen species (ROS) play a pivotal role in multiple events during the progression of intervertebral disc degeneration (IDD). Hence, the precision treatment targets associated with ROS should be further explored to promote developing effective therapeutic strategies. In this study, by analyzing specimens from patients and RNA sequencing of ROS-induced human primary nucleus pulposus cells (NPCs), osteopontin (OPN) and ferroptosis were identified as critical molecular entities and cellular pathways implicated in ROS-mediated IDD. Subsequent animal models and cellular assays determined that ROS induced upregulation of OPN, which in turn triggered ferroptosis in NPCs and intervertebral discs, consequently leading to IDD. Building upon these findings, a comprehensive screening of molecular drug database revealed that quercetin, an antioxidant molecule compound, possesses the capacity to couple OPN, thereby mitigating OPN-induced ferroptosis and IDD. In addition, the compound of quercetin for targeting OPN was encapsulated in phenylboric acid modified dendrimer (G3-PBA) nanoparticles to improve its solubility, and then embedded in a ROS-degradable and injectable hydrogel, thereby achieving on-demand release of quercetin with the progression of IDD. Collectively, this study not only identified a novel therapeutic target, but also engineered an effective therapeutic strategy intended for the autonomous management of IDD.

Indexed as

FerroptosisHydrogelsIntervertebral Disc DegenerationOsteopontinQuercetinAnimalsAntioxidantsCells, CulturedHumansMaleNanoparticlesNucleus PulposusReactive Oxygen SpeciesAntioxidantsHydrogelsOsteopontinQuercetinReactive Oxygen SpeciesFerroptosisInjectable hydrogelIntervertebral disc degenerationOsteopontinQuercetin

Identifiers

PMID40624664
PMCPMC12235785

What OpenQuestion holds

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Registered trials

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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.