Lysophosphatidic Acid Receptor Antagonists and Cancer: The Current Trends, Clinical Implications, and Trials.
Yu-Hsuan LinYueh-Chien LinChien-Chin ChenPublished in: Cells (2021)
Lysophosphatidic acid (LPA) is a bioactive lipid mediator primarily derived from membrane phospholipids. LPA initiates cellular effects upon binding to a family of G protein-coupled receptors, termed LPA receptors (LPAR1 to LPAR6). LPA signaling drives cell migration and proliferation, cytokine production, thrombosis, fibrosis, angiogenesis, and lymphangiogenesis. Since the expression and function of LPA receptors are critical for cellular effects, selective antagonists may represent a potential treatment for a broad range of illnesses, such as cardiovascular diseases, idiopathic pulmonary fibrosis, voiding dysfunctions, and various types of cancers. More new LPA receptor antagonists have shown their therapeutic potentials, although most are still in the preclinical trial stage. This review provided integrative information and summarized preclinical findings and recent clinical trials of different LPA receptor antagonists in cancer progression and resistance. Targeting LPA receptors can have potential applications in clinical patients with various diseases, including cancer.
Keyphrases
- papillary thyroid
- idiopathic pulmonary fibrosis
- clinical trial
- cell migration
- squamous cell
- cardiovascular disease
- squamous cell carcinoma
- lymph node metastasis
- randomized controlled trial
- fatty acid
- cell therapy
- drug delivery
- study protocol
- climate change
- signaling pathway
- human health
- binding protein
- double blind
- open label