دورية أكاديمية

Therapeutic potential of ASK1 activators in cancer treatment: Current insights and future directions

التفاصيل البيبلوغرافية
العنوان: Therapeutic potential of ASK1 activators in cancer treatment: Current insights and future directions
المؤلفون: Bo Wang, Ying Ma, Yue Zhang, Xunzhe Yin
المصدر: Biomedicine & Pharmacotherapy, Vol 178, Iss , Pp 117214- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: ASK1, Apoptosis, Cancer, MAP3K, JNK signaling pathway, P38 MAPK signaling pathway, Therapeutics. Pharmacology, RM1-950
الوصف: Apoptosis signal-regulated kinase 1 (ASK1) is a member of the mitogen-activated protein kinase kinase (MAP3K) family, whose activation and regulation are intricately associated with apoptosis. ASK1 is activated in response to oxidative stress, among other stimuli, subsequently triggering downstream JNK, p38 MAPK, and mitochondria-dependent apoptotic signaling, which participate in the initiation of tumor cell apoptosis induced by various stimuli. Research has shown that ASK1 plays a crucial role in the apoptosis of lung cancer, breast cancer, and liver cancer cells. Currently, the investigation of effective ASK1 activators is a hot topic in research on tumor cell apoptosis. Synthetic compounds such as human β-defensin, triazolothiazide derivatives and heat shock protein 27 inhibitors; natural compounds such as quercetin, Laminarina japonica polysaccharide-1 peptide and theabrownin; and nanomedicines such as cerium oxide nanoparticles, magnetite FeO nanoparticles and silver nanoparticles can activate ASK1 and induce apoptosis in various tumor cells. This review extensively investigates the roles and activation mechanisms of ASK1, explores its impact on a variety of apoptotic signaling pathways, and discusses the potential therapeutic applications of various ASK1 activators in cancer treatment. In addition, this paper provides an in-depth discussion of the future development of this field and proposes a promising method for further research and clinical progress.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0753-3322
Relation: http://www.sciencedirect.com/science/article/pii/S0753332224010989; https://doaj.org/toc/0753-3322
DOI: 10.1016/j.biopha.2024.117214
URL الوصول: https://doaj.org/article/008d9042ae1647d8b83f1564007d11b2
رقم الأكسشن: edsdoj.008d9042ae1647d8b83f1564007d11b2
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:07533322
DOI:10.1016/j.biopha.2024.117214