دورية أكاديمية

Role of Forkhead Box O Transcription Factors in Oxidative Stress-Induced Chondrocyte Dysfunction: Possible Therapeutic Target for Osteoarthritis?

التفاصيل البيبلوغرافية
العنوان: Role of Forkhead Box O Transcription Factors in Oxidative Stress-Induced Chondrocyte Dysfunction: Possible Therapeutic Target for Osteoarthritis?
المؤلفون: Rikang Wang, Shuai Zhang, Rahul Previn, Di Chen, Yi Jin, Guangqian Zhou
المصدر: International Journal of Molecular Sciences, Vol 19, Iss 12, p 3794 (2018)
بيانات النشر: MDPI AG, 2018.
سنة النشر: 2018
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: chondrocyte dysfunction, osteoarthritis, FoxO, oxidative stress, autophagy, aging, articular cartilage, molecular target, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: Chondrocyte dysfunction occurs during the development of osteoarthritis (OA), typically resulting from a deleterious increase in oxidative stress. Accordingly, strategies for arresting oxidative stress-induced chondrocyte dysfunction may lead to new potential therapeutic targets for OA treatment. Forkhead box O (FoxO) transcription factors have recently been shown to play a protective role in chondrocyte dysfunction through the regulation of inflammation, autophagy, aging, and oxidative stress. They also regulate growth, maturation, and matrix synthesis in chondrocytes. In this review, we discuss the recent progress made in the field of oxidative stress-induced chondrocyte dysfunction. We also discuss the protective role of FoxO transcription factors as potential molecular targets for the treatment of OA. Understanding the function of FoxO transcription factors in the OA pathology may provide new insights that will facilitate the development of next-generation therapies to prevent OA development and to slow OA progression.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1422-0067
Relation: https://www.mdpi.com/1422-0067/19/12/3794; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms19123794
URL الوصول: https://doaj.org/article/8639a47ccd224ffe977f9ae31ea825d5
رقم الأكسشن: edsdoj.8639a47ccd224ffe977f9ae31ea825d5
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14220067
DOI:10.3390/ijms19123794