金属蛋白酶-7在特发性肺纤维化中的作用机制及应用进展
Mechanisms and application progress of metalloproteinase-7 in idiopathic pulmonary fibrosis
郭春旭 1张子璇 1杜丽娟 2闫莉2
作者信息
- 1. 河北医科大学研究生院,石家庄 050000
- 2. 河北省人民医院呼吸与危重症医学科,石家庄 050000
- 折叠
摘要
特发性肺纤维化是一种预后不良的慢性纤维化性间质性肺疾病,病因不明,早期诊断、准确评估病情、及早进行临床干预,能够改善患者预后.基质金属蛋白酶-7是肺损伤后肺泡上皮细胞分泌的活性介质,对预测特发性肺纤维化的预后表现突出,也在靶向治疗上存在研究价值.基质金属蛋白酶-7区别于其他基质金属蛋白酶成员的结构及核苷酸组成的多态性,二者导致了其作用范围广泛,浓度上调高效.了解基质金属蛋白酶-7的临床应用及作用通路,探究抑制其浓度能否使特发性肺纤维化患者获益,可为早期控制疾病的发生发展提供新思路.
Abstract
Idiopathic pulmonary fibrosis is a chronic fibrotic interstitial lung disease with a poor prognosis and unknown etiology.Early diagnosis,accurate disease assessment,and timely clinical intervention can improve patient's outcomes.Matrix metalloproteinase-7 is an active mediator secreted by alveolar epithelial cells after lung injury.It is notable for its role in predicting the prognosis of idiopathic pulmonary fibrosis and has research value in targeted therapy.The structural and nucleotide composition polymorphisms that distinguish matrix metalloproteinase-7 from other matrix metalloproteinase members,lead its broad functional range and efficient up-regulation.By understanding the clinical applications and action pathways of matrix metalloproteinase-7,the study exploring whether inhibiting its concentration could benefit idiopathic pulmonary fibrosis patients could provide new insights for early disease control.
关键词
特发性肺纤维化/基质金属蛋白酶-7/金属蛋白酶组织抑制剂/作用机制/生物标志物Key words
idiopathic pulmonary fibrosis/matrix metalloproteinase-7/tissue inhibitors of metalloproteinases/mechanism of action/biomarkers引用本文复制引用
基金项目
河北省医学科学研究课题计划(20230300)
出版年
2024
国家科技期刊平台
NSTL
万方数据