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Formulation Redesigning of Itaconate Treats Periodontitis via Nrf2/TFAM-Mediated Reprogramming of Mitochondrial Metabolism
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作者 Yanqun Liu Baosheng Li +8 位作者 Jingyi Duan Tianyang Han Fengming Ye Huan Xia Yanzhen Ou Xiaoyu Li Qing Cai Weiyan Meng Shoujun Zhu 《SmartMat》 2025年第4期93-115,共23页
Periodontitis is the leading cause of tooth loss in adults.Unfortunately,inflammation remains poorly controlled and prone to relapse,even after removing the initial plaque biofilm.The unique metabolic properties of mi... Periodontitis is the leading cause of tooth loss in adults.Unfortunately,inflammation remains poorly controlled and prone to relapse,even after removing the initial plaque biofilm.The unique metabolic properties of mitochondria in the periodontal microenvironment provide a promising target for novel therapeutic strategies against periodontitis.Here,we integrate meta-bolomics and network biology to elucidate the potential role of nuclear factor E2-related factor 2/mitochondrial transcription factor(Nrf2/TFAM)in regulating mitochondrial metabolism in periodontitis.Based on this discovery,it is crucial to develop an innovative nanomedicine capable of effectively modulating the mitochondrial metabolism in periodontitis.Recently,itaconate(ITA),a key metabolite linking mitochondrial metabolism and inflammation,has emerged as a powerhouse in regulating immunity through Nrf2;however,its limited permeability hinders its application in biological systems.Therefore,we synthesize ITA-based nano cocktail(INC)with cell permeability and improved biological functions.At the cellular level,INC activates Nrf2/TFAM to remodel mitochondrial metabolism and regulate macrophage immune homeostasis.In mouse models of peri-odontitis,INC successfully reprograms mitochondrial metabolism within the gingiva,leading to an improved inflammatory microenvironment.Our study elucidates the role of INC in modulating mitochondrial metabolism,thereby offering an inno-vative therapeutic strategy for the management of periodontitis and other clinical conditions resulting from mitochondrial abnormalities. 展开更多
关键词 itaconate-based nano cocktail macrophages polarization mitochondrial metabolism nrf2/tfam PERIODONTITIS
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Nrf2与TFAM共同影响前列腺癌的发生发展 被引量:1
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作者 郝斌 苗志刚 +1 位作者 袁媛 季德才 《基因组学与应用生物学》 CAS CSCD 北大核心 2017年第12期5027-5032,共6页
为了研究人类核转录因子红细胞系2p45相关因子(nuclear factor erythrioid-2p45 related factor 2,Nrf2)与线粒体转录因子A(mitochondrial transcription factor A,TFAM)对前列腺癌发生发展的影响,本研究选取了本院2014年4月至2016年4... 为了研究人类核转录因子红细胞系2p45相关因子(nuclear factor erythrioid-2p45 related factor 2,Nrf2)与线粒体转录因子A(mitochondrial transcription factor A,TFAM)对前列腺癌发生发展的影响,本研究选取了本院2014年4月至2016年4月52例经手术切除或经病理穿刺得到的前列腺癌组织标本作为研究对象,通过免疫组化检测了Nrf2与TFAM在前列腺癌组织中的表达情况,并应用Spearman等级相关分析验证了Nrf2、TFAM表达强度与Gleason评分的关系以及Nrf2表达强度与TFAM表达强度之间的关系。研究发现,Nrf2表达强度与Gleason评分呈正相关关系(p=0.007),相关系数r=0.471,相关性具有统计学意义(p=0.007);TFAM表达强度与Gleason评分呈正相关关系,相关系数r=0.623,相关性具有统计学意义(p=0.000);Nrf2与TFAM二者表达情况呈正相关关系,相关系数r=0.482,相关性具有统计学意义(p=0.003)。我们的研究证明了Nrf2与TFAM二者是前列腺癌的发生发展的因素之一,且Nrf2与TFAM可能通过同一通路参与前列腺癌的发生发展。 展开更多
关键词 nrf2 tfam 前列腺癌
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