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热休克蛋白对缺氧缺血性脑损伤神经元凋亡的保护作用及机制 被引量:2
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作者 刘玲 《国外医学(儿科学分册)》 2003年第3期121-123,共3页
热休克蛋白(HSP)是机体在受到应激刺激后诱导产生的一组蛋白质,对细胞损伤具有保护作用。近年来较多文献报道HSP对缺氧缺血性脑损伤神经元的凋亡具有保护作用。本文就HSP的特点、脑缺氧缺血后神经元中HSP的表达及其对神经元凋亡的保护... 热休克蛋白(HSP)是机体在受到应激刺激后诱导产生的一组蛋白质,对细胞损伤具有保护作用。近年来较多文献报道HSP对缺氧缺血性脑损伤神经元的凋亡具有保护作用。本文就HSP的特点、脑缺氧缺血后神经元中HSP的表达及其对神经元凋亡的保护作用和机制进行综述。 展开更多
关键词 缺氧缺血性脑损伤 神经元凋亡 热休克蛋白 线粒体 应激激活激酶途径 p53基因 BAX基因 BCL-2基因 核转录因子
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Inflammation-and stress-related signaling pathways in hepatocarcinogenesis 被引量:19
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作者 Hayato Nakagawa Shin Maeda 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第31期4071-4081,共11页
It has been established that cancer can be promoted and exacerbated by inflammation.Hepatocellular carcinoma(HCC) is the fifth most common cancer worldwide,and its long-term prognosis remains poor.Although HCC is a co... It has been established that cancer can be promoted and exacerbated by inflammation.Hepatocellular carcinoma(HCC) is the fifth most common cancer worldwide,and its long-term prognosis remains poor.Although HCC is a complex and heterogeneous tumor with several genomic mutations,it usually develops in the context of chronic liver damage and inflammation,suggesting that understanding the mechanism(s) of inflammation-mediated hepatocarcinogenesis is essential for the treatment and prevention of HCC.Chronic liver damage induces a persistent cycle of necroinflammation and hepatocyte regeneration,resulting in genetic mutations in hepatocytes and expansion of initiated cells,eventually leading to HCC development.Recently,several inflammation-and stress-related signaling pathways have been identified as key players in these processes,which include the nuclear factor B,signal transducer and activator of transcription,and stress-activated mitogen-activated protein kinase pathways.Although these pathways may suggest potential therapeutic targets,they have a wide range of functions and complex crosstalk occurs among them.This review focuses on recent advances in our understanding of the roles of these signaling pathways in hepatocarcinogenesis. 展开更多
关键词 Hepatocellular carcinoma INFLAMMATION Nuclear factor-~B Mitogen-activated protein kinase Signal transducer and activator of transcription c-JunNH2-terminal kinase P38 Transforming growth factor-activated kinase 1 Apoptosis signal-regulating kinase 1
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氟斑牙发病分子信号通路研究进展
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作者 王欣蕊 白国辉 田源 《中华地方病学杂志》 CAS 北大核心 2023年第2期159-164,共6页
氟斑牙是儿童时期摄入过量氟化物而引起的慢性口腔氟中毒表现。目前氟斑牙发病的分子机制尚不明确。成釉细胞是牙齿组织中对氟化物最敏感的细胞,氟通过对分子信号通路中关键分子的作用,影响成釉细胞增殖和分泌功能,导致氟斑牙形成。本... 氟斑牙是儿童时期摄入过量氟化物而引起的慢性口腔氟中毒表现。目前氟斑牙发病的分子机制尚不明确。成釉细胞是牙齿组织中对氟化物最敏感的细胞,氟通过对分子信号通路中关键分子的作用,影响成釉细胞增殖和分泌功能,导致氟斑牙形成。本文综述了近年来分子信号通路[丝裂原活化蛋白激酶(MAPK)、转化生长因子-β(TGF-β)/Smad、Wnt、Foxo1/Runx2]及应激途径(内质网应激及氧化应激)与氟斑牙发生的关系,以期在分子层面上,深入了解氟斑牙的发病机制,为氟斑牙的防治提供新思路。 展开更多
关键词 氟中毒 信号通路 应激途径
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