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The Role of Lysophospholipid Metabolites LPC and LPA in the Pathogenesis of Chronic Obstructive Pulmonary Disease.
Zhou, Qiqiang; Chen, Yahong; Liang, Ying; Sun, Yongchang.
Affiliation
  • Zhou Q; Department of Respiratory and Critical Care Medicine, Peking University Third Hospital, Beijing 100191, China.
  • Chen Y; Department of Respiratory and Critical Care Medicine, Peking University Third Hospital, Beijing 100191, China.
  • Liang Y; Research Center for Chronic Airway Diseases, Peking University Health Science Center, Beijing 100191, China.
  • Sun Y; Department of Respiratory and Critical Care Medicine, Peking University Third Hospital, Beijing 100191, China.
Metabolites ; 14(6)2024 May 31.
Article in En | MEDLINE | ID: mdl-38921452
ABSTRACT
Chronic obstructive pulmonary disease (COPD) is a heterogeneous lung condition characterized by persistent respiratory symptoms and airflow limitation. While there are some available treatment options, the effectiveness of treatment varies depending on individual differences and the phenotypes of the disease. Therefore, exploring or identifying potential therapeutic targets for COPD is urgently needed. In recent years, there has been growing evidence showing that lysophospholipids, namely lysophosphatidylcholine (LPC) and lysophosphatidic acid (LPA), can play a significant role in the pathogenesis of COPD. Exploring the metabolism of lysophospholipids holds promise for understanding the underlying mechanism of COPD development and developing novel strategies for COPD treatment. This review primarily concentrates on the involvement and signaling pathways of LPC and LPA in the development and progression of COPD. Furthermore, we reviewed their associations with clinical manifestations, phenotypes, and prognosis within the COPD context and discussed the potential of the pivotal signaling molecules as viable therapeutic targets for COPD treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Metabolites Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Metabolites Year: 2024 Document type: Article Affiliation country: