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肺纤维化信号调控通路的研究进展 被引量:2

Research progress of signal transduction pathways of pulmonary fibrosis
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摘要 肺纤维化作为一种慢性肺部疾病,患者被确诊的时间普遍在疾病的中后期,因此失去了最佳治疗时间,从而增加了患者的病死率。如果能在早期发现肺纤维化疾病的发病趋势,识别疾病特征,就能在最佳治疗时间采取相应的治疗方案,减少患者的痛苦,增加存活率。本文以目前对肺纤维化的研究作为出发点,探讨疾病的发展过程,再结合相关信号调节通路,为尽早确诊疾病和制定治疗方案提供可能性。 Pulmonary fibrosis, a chronic lung disease, is always diagnosed at middle or later stage of the disease, of which mortality is increased due to missing the best treatment period. However, if the tendency and characteristics of pulmonary fibrosis are identified at earlier stage, the corresponding therapeutic schedule would be adopted for patients at the best treatment period, which would decrease their suffering and increase their survival rate. On the basis of the previous studies on pulmonary fibrosis, this paper explores the developing process of the diseases and the corresponding signaling pathways, which provides the possibility for diagnosing the disease and formulating the effective therapeutic schedule as early as possible.
出处 《国际呼吸杂志》 2018年第4期311-314,共4页 International Journal of Respiration
基金 广西科技厅项目(11-031-05-Z1) 广西教育厅广西研究生教育创新计划资助项目(JGY2014086) 广西教育厅研究生教育创新课题计划资助项目(YJSP201706) 广西中医药药效重点实验室建设项目(11-031-05)
关键词 肺纤维化 发病机制 信号通路 自噬 Pulmonary fibrosis Pathogenesis Signal pathway Autophagy
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  • 1刘永琦,李金田,李娟,张毅,颜春鲁,杨军,宋华平.黄芪对肺纤维化大鼠Th1/Th2型细胞因子平衡及自由基代谢的影响[J].免疫学杂志,2009,25(3):290-292. 被引量:45
  • 2Pardo A,Selman M. Role of matrix metaloproteases in idiopathic pulmonary fibrosis[J].Fibrogenesis Tissue Repair,2012,5(Suppl 1): S9.
  • 3Sakai N,Tager A M. Fibrosis of two: epithelial cellfibroblast interactions inpulmonary fibrosis[J].Biochim Biophys Acta,2013,1832(7): 911-921.
  • 4Raghu G,Collard H R,Egan J J,et al. An official ATS/ ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management[J]. Am J RespirCrit Care Med,2011,183(6): 788-824.
  • 5Keogh B A,Crystal R G. Alveolitis: the key to the interstitial lung disorders[J].Thorax,1982,37(1): 1-10.
  • 6Selman M,King T E,Pardo A,et al. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy[J].Ann Intern Med,2001,134 (2): 136-151.
  • 7Hyde D M,King T E Jr,McDermott T,et al. Idiopathic pulmonary fibrosis. Quantitative assessment of lung pathology. Comparison of a semiquantitative and a morphometric histopathologic scoring system[J].Am Rev Respir Dis,1992,146(4): 1042-1047.
  • 8Wu Z,Yang L,Cai L,et al. Detection of epithelial to mesenchymal transition in airways of a bleomycin induced pulmonary fibrosis model derived from an alpha-smooth muscle actin-Cre transgenic mouse[J].Respir Res,2007,8: 1.
  • 9King T E Jr,Schwarz M I,Brown K,et al. Idiopathic pulmonary fibrosis: relationship between histopathologic features and mortality[J].Am J RespirCrit Care Med,2001,164(6): 1025-1032.
  • 10Moeller A,Gilpin S E,Ask K,et al. Circulating fibrocytes are an indicator of poor prognosis in idiopathic pulmonary fibrosis[J].Am J Respir Crit Care Med,2009,179(7): 588-594.

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