Inhibition of lysophosphatidic acid receptor 6 upregulated by the choline‐deficient l‐amino acid‐defined diet prevents hepatocarcinogenesis in mice. Issue 5 (8th February 2023)

• Record Type: Journal Article
• Authors: Gnocchi, Davide; Afonso, Marta B.; Cavalluzzi, Maria Maddalena; Lentini, Giovanni; Ingravallo, Giuseppe; Sabbà, Carlo; Rodrigues, Cecilia M. P.; Mazzocca, Antonio
• Is Part Of: Molecular carcinogenesis. Volume 62:Issue 5(2023)
• Page Start: 577
• Page End: 582
• Publication Date: 2023-02-08
• Subjects: hepatic metabolism -- hepatocellular carcinoma -- LPAR6 -- lysophosphatidic acid -- NAFLD -- NASH; Carcinogenesis -- Molecular aspects -- Periodicals; 616.994071
• DOI: 10.1002/mc.23516
• Languages: English
• ISSNs: 0899-1987

Abstract

Abstract: Hepatocellular carcinoma (HCC) is one of the most worrying tumors worldwide today, and its epidemiology is on the rise. Traditional pharmacological approaches have shown unfavorable results and exhibited many side effects. Hence, there is a need for new efficacious molecules with fewer side effects and improvements on traditional approaches. We previously showed that lysophosphatidic acid (LPA) supports hepatocarcinogenesis, and its effects are mainly mediated by LPA receptor 6 (LPAR6). We also reported that 9‐xanthylacetic acid (XAA) acts as an antagonist of LPAR6 to inhibit the growth of HCC. Here, we report that LPAR6 is involved in the choline‐deficient l ‐amino acid‐defined (CDAA) diet‐induced hepatocarcinogenesis in mice. Our data demonstrate that CDAA diet‐induced metabolic imbalance stimulates LPAR6 expression in mice and that XAA counteracts diet‐induced effects on hepatic lipid accumulation, fibrosis, inflammation, and HCC development. These conclusions are corroborated by results on LPAR6 gain and loss‐of‐function in HCC cells.