Extracecellulr vesicles (EVs) microRNAs (miRNAs) derived from mesenchymal stem cells (MSCs) in osteoarthritis (OA); detailed role in pathogenesis and possible therapeutics DOI Creative Commons
Seyede Sara Pakdaman Kolour,

Saeide Nematollahi,

Masoud Dehbozorgi

et al.

Heliyon, Journal Year: 2025, Volume and Issue: unknown, P. e42258 - e42258

Published: Jan. 1, 2025

Language: Английский

Osteoarthritis: pathogenic signaling pathways and therapeutic targets DOI Creative Commons
Qing Yao, Xiaohao Wu, Chu Tao

et al.

Signal Transduction and Targeted Therapy, Journal Year: 2023, Volume and Issue: 8(1)

Published: Feb. 3, 2023

Abstract Osteoarthritis (OA) is a chronic degenerative joint disorder that leads to disability and affects more than 500 million population worldwide. OA was believed be caused by the wearing tearing of articular cartilage, but it now commonly referred as whole-joint initiated with biochemical cellular alterations in synovial tissues, which histological structural changes ends up whole tissue dysfunction. Currently, there no cure for OA, partly due lack comprehensive understanding pathological mechanism initiation progression disease. Therefore, better signaling pathways key molecules involved pathogenesis crucial therapeutic target design drug development. In this review, we first summarize epidemiology including its prevalence, incidence burdens, risk factors. We then focus on roles regulation pathways, such Wnt/β-catenin, NF-κB, focal adhesion, HIFs, TGFβ/ΒΜP FGF regulators AMPK, mTOR, RUNX2 onset development OA. addition, factors associated MMPs, ADAMTS/ADAMs, PRG4, are discussed detail. Finally, provide updates current clinical therapies trials biological treatments drugs Research advances basic knowledge cartilage biology will have significant impact translational value developing strategies.

Language: Английский

Citations

564

A DNA tetrahedron-based ferroptosis-suppressing nanoparticle: superior delivery of curcumin and alleviation of diabetic osteoporosis DOI Creative Commons
Yong Li, Zhengwen Cai, Wenjuan Ma

et al.

Bone Research, Journal Year: 2024, Volume and Issue: 12(1)

Published: Feb. 29, 2024

Abstract Diabetic osteoporosis (DOP) is a significant complication that poses continuous threat to the bone health of patients with diabetes; however, currently, there are no effective treatment strategies. In diabetes, increased levels ferroptosis affect osteogenic commitment and differentiation mesenchymal stem cells (BMSCs), leading skeletal changes. To address this issue, we aimed target propose novel therapeutic approach for DOP. We synthesized ferroptosis-suppressing nanoparticles, which could deliver curcumin, natural compound, marrow using tetrahedral framework nucleic acid (tFNA). This delivery system demonstrated excellent curcumin bioavailability stability, as well synergistic properties tFNA. Both in vitro vivo experiments revealed nanoparticles enhance mitochondrial function by activating nuclear factor E2-related 2 (NRF2)/glutathione peroxidase 4 (GPX4) pathway, inhibiting ferroptosis, promoting BMSCs diabetic microenvironment, reducing trabecular loss, increasing formation. These findings suggest curcumin-containing DNA tetrahedron-based have promising potential DOP other ferroptosis-related diseases.

Language: Английский

Citations

74

Risk of metabolic abnormalities in osteoarthritis: a new perspective to understand its pathological mechanisms DOI Creative Commons
Guizheng Wei, Ke Lu, Muhammad Ihtisham Umar

et al.

Bone Research, Journal Year: 2023, Volume and Issue: 11(1)

Published: Dec. 6, 2023

Abstract Although aging has traditionally been viewed as the most important risk factor for osteoarthritis (OA), an increasing amount of epidemiological evidence highlighted association between metabolic abnormalities and OA, particularly in younger individuals. Metabolic abnormalities, such obesity type II diabetes, are strongly linked to they affect both weight-bearing non-weight-bearing joints, thus suggesting that pathogenesis OA is more complicated than mechanical stress induced by overweight. This review aims explore recent advances research on relationship risk, including impact abnormal glucose lipid metabolism, potential targeted therapeutic strategies.

Language: Английский

Citations

59

Iron homeostasis and ferroptosis in human diseases: mechanisms and therapeutic prospects DOI Creative Commons

Qin Ru,

Yusheng Li,

Lin Chen

et al.

Signal Transduction and Targeted Therapy, Journal Year: 2024, Volume and Issue: 9(1)

Published: Oct. 14, 2024

Iron, an essential mineral in the body, is involved numerous physiological processes, making maintenance of iron homeostasis crucial for overall health. Both overload and deficiency can cause various disorders human diseases. Ferroptosis, a form cell death dependent on iron, characterized by extensive peroxidation lipids. Unlike other kinds classical unprogrammed death, ferroptosis primarily linked to disruptions metabolism, lipid peroxidation, antioxidant system imbalance. Ferroptosis regulated through transcription, translation, post-translational modifications, which affect cellular sensitivity ferroptosis. Over past decade or so, diseases have been as part their etiology, including cancers, metabolic disorders, autoimmune diseases, central nervous cardiovascular musculoskeletal Ferroptosis-related proteins become attractive targets many major that are currently incurable, some regulators shown therapeutic effects clinical trials although further validation potential needed. Therefore, in-depth analysis its molecular mechanisms may offer additional strategies prevention treatment. In this review, we discuss significance contribution etiology development along with evidence supporting targeting approach. Importantly, evaluate recent promising interventions, providing guidance future targeted treatment therapies against

Language: Английский

Citations

56

Cardamonin alleviates chondrocytes inflammation and cartilage degradation of osteoarthritis by inhibiting ferroptosis via p53 pathway DOI

Ziheng Gong,

Yanjie Wang, Lan Li

et al.

Food and Chemical Toxicology, Journal Year: 2023, Volume and Issue: 174, P. 113644 - 113644

Published: Jan. 30, 2023

Language: Английский

Citations

55

The Role of Regulated Programmed Cell Death in Osteoarthritis: From Pathogenesis to Therapy DOI Open Access
Suqing Liu, Yurong Pan, Ting Li

et al.

International Journal of Molecular Sciences, Journal Year: 2023, Volume and Issue: 24(6), P. 5364 - 5364

Published: March 10, 2023

Osteoarthritis (OA) is a worldwide chronic disease that can cause severe inflammation to damage the surrounding tissue and cartilage. There are many different factors lead osteoarthritis, but abnormally progressed programmed cell death one of most important risk induce osteoarthritis. Prior studies have demonstrated death, including apoptosis, pyroptosis, necroptosis, ferroptosis, autophagy, cuproptosis, has great connection with In this paper, we review role types in generation development OA how signal pathways modulate regulate OA. Additionally, provides new insights into radical treatment osteoarthritis rather than conservative treatment, such as anti-inflammation drugs or surgical operation.

Language: Английский

Citations

42

Hypoxia and Matrix Metalloproteinase 13‐Responsive Hydrogel Microspheres Alleviate Osteoarthritis Progression In Vivo DOI
Tong Zhou, Hao Xiong, Shunyu Yao

et al.

Small, Journal Year: 2023, Volume and Issue: 20(19)

Published: Dec. 6, 2023

Abstract The occurrence of osteoarthritis (OA) is highly associated with the inflammatory hypoxic microenvironment. Yet currently no attention has been paid to fabricating hypoxia‐responsive platforms for OA treatment. Herein, an injectable hydrogel microsphere system (HAM‐SA@HCQ) focusing on inflamed joint prepared methacrylate‐modified sulfonated azocalix[4]arene (SAC4A‐MA), methacrylated hyaluronic acid (HA‐MA), and dithiol‐terminated matrix metalloproteinase 13 (MMP‐13) sensitive peptide via a microfluidic device photo crosslinking technique, followed by encapsulation anti‐inflammatory drug hydroxychloroquine (HCQ) through host–guest interaction. Owing hydrophobic deep cavity, phenolic units, azo bonds SAC4A‐MA, microspheres show strong loading capacity, prominent reactive oxygen species (ROS) scavenging capability, specific release ability. In tissue microenvironment, undergo degradation excessive MMP‐13 HCQ under hypoxia condition, which synergizes ROS‐scavenging calixarene inhibit response macrophages. After being injected into OA‐inflamed joint, HAM‐SA@HCQ can significantly attenuate oxidative stress, downregulate expression hypoxia‐induced factor‐1α cytokines, prevent cartilage from destroyed.

Language: Английский

Citations

29

Recent Advances in Cellular Signaling Interplay between Redox Metabolism and Autophagy Modulation in Cancer: An Overview of Molecular Mechanisms and Therapeutic Interventions DOI Creative Commons
Md. Ataur Rahman, Kazi Rejvee Ahmed,

Farzana Haque

et al.

Antioxidants, Journal Year: 2023, Volume and Issue: 12(2), P. 428 - 428

Published: Feb. 9, 2023

Autophagy is a fundamental homeostatic process in which certain cellular components are ingested by double-membrane autophagosomes and then degraded to create energy or maintain homeostasis survival. It typically observed nutrient-deprived cells as survival mechanism. However, it has also been identified crucial maintaining disease progression. Normal metabolism produces reactive oxygen (ROS) nitrogen species at low levels. increased production causes oxidative stress, can lead diabetes, cardiovascular diseases, neurological disorders, cancer. was recently shown that redox equilibrium via autophagy critical for responses stress. little understood about the molecular cancer processes connect control of autophagy. In cells, oncogenic mutations, carcinogens, metabolic reprogramming cause ROS generation Recent studies have suggested activates pathways promote development metastasis. Moreover, relationship between programming involved malignant phenotype. Currently, while signaling events governing how affects cascades well understood, very known related this review, we focus on current knowledge modulation role further stress progression regulation. Therefore, review focuses understanding oxidation/reduction fine-tune help understand govern cancer, either leading cell death strategies

Language: Английский

Citations

25

Undenatured type II collagen and its role in improving osteoarthritis DOI
Rong Xu, Jian Wu, Lin Zheng

et al.

Ageing Research Reviews, Journal Year: 2023, Volume and Issue: 91, P. 102080 - 102080

Published: Sept. 27, 2023

Language: Английский

Citations

25

Supramolecular self-assembly of EGCG-selenomethionine nanodrug for treating osteoarthritis DOI Creative Commons

Haichao Yu,

Zelong Song,

Jie Yu

et al.

Bioactive Materials, Journal Year: 2023, Volume and Issue: 32, P. 164 - 176

Published: Oct. 9, 2023

Osteoarthritis (OA) has emerged as a significant health concern among the elderly population, with increasing attention paid to ferroptosis-induced OA in recent years. However, prolonged use of nonsteroidal anti-inflammatory drugs or corticosteroids can lead series side effects and limited therapeutic efficacy. This study aimed employ Mannich condensation reaction between epigallocatechin-3-gallate (EGCG) selenomethionine (SeMet) efficiently synthesize polyphenol-based nanodrugs aqueous media for treating OA. Molecular biology experiments demonstrated that EGCG-based (ES NDs) could effectively reduce glutathione peroxidase 4 (GPX4) inactivation, abnormal Fe2+ accumulation, lipid peroxidation induced by oxidative stress, which ameliorated metabolic disorder chondrocytes other multiple pathological processes triggered ferroptosis. Moreover, imaging histopathological analysis destabilization medial meniscus model mice confirmed ES NDs exhibiting relieving The intra-articular delivery represents promising approach joint inflammatory diseases.

Language: Английский

Citations

25