PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 14, 2026Scientific Reports0 citationsOpen Access

Plasma acylcarnitine dysregulation associated with CPT1-mediated metabolism contributes to oral carcinogenesis

YKYeon-Hee KimSCSung Weon ChoiJLJong Ho Lee

Key Points

  • This research aims to explore the link between lipid metabolic alterations and oral carcinogenesis.
  • Conducted semi-targeted and targeted plasma metabolomic profiling in a cohort of 182 oral cancer patients and 364 healthy controls, followed by validation in an external cohort of 52 pairs.
  • Utilized machine learning approaches to identify plasma metabolites differentiating oral cancer patients from healthy controls.
  • Analyzed the expression of carnitine palmitoyltransferase 1 (CPT1) in tissues and pharmacologically inhibited CPT1 in oral cancer cells.
  • Three medium-chain acylcarnitines were significantly downregulated in oral cancer plasma (AUC = 0.941, 95% CI: 0.877–0.988).
  • Elevated CPT1 expression was observed in oral cancer tissues and cells, linking it to impaired lipid metabolism.
  • Pharmacological inhibition of CPT1 suppressed oral cancer cell growth and adjusted acylcarnitine levels.

Abstract

Growing evidence suggests that lipid metabolic reprogramming occurs in oral cancer (OC). We characterized circulating metabolic alterations associated with lipid metabolic reprogramming in OC. Semi-targeted and targeted plasma metabolomic profiling was performed in a discovery cohort (182 OC, 364 healthy controls HC) followed by independent external validation (52 OC, 52 HC). Machine learning approaches were used to identify plasma metabolites with strong discriminatory performance between patients with OC and healthy controls. Targeted validation confirmed consistent metabolic changes. Namely, three medium-chain acylcarnitines—decanoyl-, octanoyl-, and hexanoylcarnitine—were markedly downregulated in OC plasma, demonstrating consistent and reproducible discrimination during external validation (AUC = 0.941, 95% CI: 0.877–0.988). Pathway enrichment analysis further suggested altered β-oxidation and glycerophospholipid metabolism in OC. We also observed elevated carnitine palmitoyltransferase 1 (CPT1) expression in OC tissues and cells. Moreover, pharmacological inhibition of CPT1 suppressed OC cell growth and altered acylcarnitine profiles. These findings support an association between circulating acylcarnitine alterations and CPT1-related lipid metabolic reprogramming in OC. Furthermore, they provide biological context supporting the association between circulating metabolic alterations and CPT1-related lipid metabolic reprogramming in OC.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Kim et al. (2026) studied this question.

synapsesocial.com/papers/6a0567d2a550a87e60a20141https://doi.org/10.1038/s41598-026-52309-w
Ask AI
Helpful
Bookmark
Share
View Full Paper