Drug Design, Development and Therapy (Sep 2023)

Inhibition of LPA-LPAR1 and VEGF-VEGFR2 Signaling in IPF Treatment

  • Luo YL,
  • Li Y,
  • Zhou W,
  • Wang SY,
  • Liu YQ

Journal volume & issue
Vol. Volume 17
pp. 2679 – 2690

Abstract

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Ya-Li Luo,* Yan Li,* Wen Zhou, Si-Yu Wang, Yong-Qi Liu Gansu University Key Laboratory for Molecular Medicine and Chinese Medicine Prevention and Treatment of Major Diseases, Gansu University of Chinese Medicine, Lanzhou, 730000, People’s Republic of China*These authors contributed equally to this workCorrespondence: Yong-Qi Liu, School of Basic Medicine, Gansu University Key Laboratory for Molecular Medicine and Chinese Medicine Prevention and Treatment of Major Diseases, Gansu University of Chinese Medicine, Lanzhou, People’s Republic of China, Email [email protected]: Due to the complex mechanism and limited treatments available for pulmonary fibrosis, the development of targeted drugs or inhibitors based on their molecular mechanisms remains an important strategy for prevention and treatment. In this paper, the downstream signaling pathways mediated by VEGFR and LPAR1 in pulmonary cells and the role of these pathways in pulmonary fibrosis, as well as the current status of drug research on the targets of LPAR1 and VEGFR2, are described. The mechanism by which these two pathways regulate vascular leakage and collagen deposition leading to the development of pulmonary fibrosis are analyzed, and the mutual promotion of the two pathways is discussed. Here we propose the development of drugs that simultaneously target LPAR1 and VEGFR2, and discuss the important considerations in targeting and safety.Keywords: idiopathic pulmonary fibrosis, VEGFR2, LPAR1

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