ReviewFrontiers in cell and developmental biology2026
The dual role of autophagy in cartilage degradation: from mechanisms to targeted therapeutics.
Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
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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.
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Who cites it
2 citing papers in PubMed.
- Non-Telomeric Role of RAP1 in Facilitating NF-κB Activation and Driving Hepatocellular Carcinoma Progression.IUBMB life · 2026Article
- Research progress of cuproptosis, ferroptosis, apoptosis, and autophagy in knee osteoarthritis.Frontiers in cell and developmental biology · 2026Review
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Autophagy is a highly conserved cellular degradation and recycling process that plays a pivotal role in maintaining cartilage homeostasis. Normal autophagy is essential for the survival of chondrocytes and the preservation of the extracellular matrix (ECM); however, a decline in autophagic function may lead to the accumulation of damaged organelles and macromolecules, thereby reducing chondrocyte vitality and promoting apoptosis, which in turn contributes to the development of osteoarthritis (OA). This review summarizes the biological processes of autophagy, the interaction between autophagy and cartilage degeneration, as well as the interplay between autophagy and cellular senescence, apoptosis, inflammation, and oxidative stress. Furthermore, we explore key autophagic targets for the regulation of OA and discuss autophagy-targeting therapies, including mTOR inhibitors, AMPK activators, and natural products that target autophagy, along with emerging strategies aimed at modulating autophagy. Finally, the article highlights the challenges in the development of autophagy-targeting drugs for OA treatment and presents important scientific issues that warrant further investigation to guide future research.
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Registered trials
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.