Intestinal Candida albicans Promotes Hepatocarcinogenesis by Up-Regulating NLRP6

Hepatocellular carcinoma (HCC), a primary liver cancer, is closely associated with the gut microbiota. However, the role of gut fungi in the development of HCC remains unclear. The aim of this study was to explore the influence of intestinal Candida albicans on HCC. Here, We found that patients with HCC showed significantly decreased diversity of the gut mycobiome and increased abundance of C. albicans, compared to the patients with liver cirrhosis. The gavage of C. albicans in the WT models increased the tumor size and weight and influenced the plasma metabolome, which was indicated by alterations in 117 metabolites, such as L-carnitine and L-acetylcarnitine, and several KEGG enriched pathways, such as phenylalanine metabolism and citrate cycle. Moreover, the expression of nucleotide oligomerization domain-like receptor family pyrin domain containing 6 (NLRP6) in the intestinal tissues and primary intestinal epithelial cells of the WT mice interacted with C. albicans increased. Notably, the colonization of C. albicans had no effect on tumor growth in Nlrp6(-/-) mice. In conclusion, the abnormal colonization of C. albicans reprogrammed HCC metabolism and contributed to the progression of HCC dependent on NLRP6, which provided new targets for the treatment of HCC.

Automated summary

This study found that patients with hepatocellular carcinoma (HCC) had decreased diversity of the gut mycobiome and increased abundance of Candida albicans compared to patients with liver cirrhosis. The colonization of C. albicans in animal models promoted tumor growth and affected plasma metabolome. Furthermore, the expression of NLRP6 in the intestine was increased in the presence of C. albicans. However, C. albicans colonization had no effect on tumor growth in mice lacking NLRP6.