Lysophosphatidic acid receptor antagonists and cancer: the current trends, clinical implications, and trials

YH Lin, YC Lin, CC Chen - Cells, 2021 - mdpi.com
Cells, 2021mdpi.com
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 …
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.
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