Ketone Bodies Inhibit Growth of Hepatoblastoma and Rhabdoid Tumor of the Kidney Cells.

BACKGROUND/AIM: The prognosis for high-risk pediatric cancers remains poor, necessitating the development of novel therapies. The ketogenic diet (KD) has shown efficacy in various adult cancers; however, its impact on pediatric solid tumors remains underexplored. This study investigated the impact of ketone bodies (KBs) on hepatoblastoma and rhabdoid tumor of the kidney.

MATERIALS AND

METHODS

Human hepatoblastoma cell line (Huh6), human rhabdoid tumors of the kidney cell lines (G401, WT-CLS1), and human foreskin derived fibroblast cell line (HFF) were used in this study. Cells were cultured in control media, glucose-free media, and glucose-free media supplemented with acetoacetate or β-hydroxybutyrate. Cell viability was assessed using the WST-8 assay. Intracellular ATP concentrations and the expression of KBs-metabolizing enzymes, Succinyl-CoA: 3-oxoacid CoA transferase (SCOT) and 3-hydroxybutyrate dehydrogenase-1 (BDH1), were evaluated using an ATP assay and qRT-PCR, respectively.

RESULTS

The WST-8 assay demonstrated Huh6, G401, and WT-CLS1 growth inhibition in glucose-free media, which was not rescued by KBs-supplemented media. The ATP assay showed decreased intracellular ATP levels in Huh6 and G401 but not in WT-CLS1. Expression levels of SCOT and BDH1 in Huh6, G401, and WT-CLS1 cells were significantly lower than those in HFF cells.

CONCLUSION

The growth of Huh6, G401, and WT-CLS1 cells was inhibited under glucose-free conditions and not rescued by KBs. The current results strongly suggest that KD is a highly promising treatment for patients with hepatoblastoma and rhabdoid tumor of the kidney.