Answers are grounded in this paper and cite their sources.
Review examines lysine L-lactylation's role in disease and potential therapies, highlighting its impact on metabolism and chromatin.
Lysine L‐lactylation (K L‐la ) is a newly identified metabolite‐derived post‐translational modification that directly bridges cellular metabolic states to chromatin regulation and protein function. Mounting evidence shows that K L‐la has pivotal roles in transcription regulation and diverse cellular processes and is implicated in multiple pathophysiological conditions. This review comprehensively examines K L‐la across both histone and non‐histone substrates in biology and disease. We first illustrate the historical development of K L‐la and distinguish it from its isomers. We then delineate the enzymes regulating K L‐la , examine its crosstalk with other PTMs, and discuss its roles in cell signalling and other biological processes. Particular emphasis is placed on mechanisms through which K L‐la contributes to various human diseases such as cancer, viral infections, neurodegenerative disorders, cardiovascular conditions, metabolic abnormalities and immune dysregulation. Finally, we provide an in‐depth analysis of emerging therapeutic strategies targeting K L‐la and highlight future directions for translating mechanistic insights into clinical applications.
No takes yet. Share an insight, caveat, or question.
Malik et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: