Phosphorylation by IKK? Promotes the Degradation of HMGCL via NEDD4 in Lung Cancer.

Inflammation and metabolic reprogramming are hallmarks of cancer. How inflammation regulates cancer metabolism remains poorly understood. In this study, we found that 3-hydroxy-3-methylglutaryl-CoA lyase (HMGCL), the enzyme that catalyzes the catabolism of leucine and promotes the synthesis of ketone bodies, was downregulated in lung cancer. Downregulation of HMGCL was associated ...
with a larger tumor size and a shorter overall survival time. In a functional study, overexpression of HMGCL increased the content of ?-hydroxybutyrate (?-HB) and inhibited the tumorigenicity of lung cancer cells, and deletion of HMGCL promoted de novo tumorigenesis in KP (KrasG12D;P53f/f) mice. Mechanistically, tumor necrosis factor ? (TNF?) treatment decreased the HMGCL protein level, and IKK? interacted with HMGCL and phosphorylated it at Ser258, which destabilized HMGCL. Moreover, NEDD4 was identified as the E3 ligase for HMGCL and promoted its degradation. In addition, mutation of Ser258 to alanine inhibited the ubiquitination of HMGCL by NEDD4 and thus inhibited the anchorage-independent growth of lung cancer cells more efficiently than did wild-type HMGCL. In summary, this study demonstrated a link between TNF?-mediated inflammation and cancer metabolism.
Mesh Terms:
Animals, I-kappa B Kinase, Inflammation, Lung Neoplasms, Lyases, Mice, Phosphorylation, Protein Serine-Threonine Kinases, Tumor Necrosis Factor-alpha, Ubiquitin-Protein Ligases, Ubiquitination
Int J Biol Sci
Date: Mar. 17, 2023
Download Curated Data For This Publication
246955
Switch View:
  • Interactions 6