The Development of Sugar-Based Anti-Melanogenic Agents
Overview
Chemistry
Molecular Biology
Affiliations
The regulation of melanin production is important for managing skin darkness and hyperpigmentary disorders. Numerous anti-melanogenic agents that target tyrosinase activity/stability, melanosome maturation/transfer, or melanogenesis-related signaling pathways have been developed. As a rate-limiting enzyme in melanogenesis, tyrosinase has been the most attractive target, but tyrosinase-targeted treatments still pose serious potential risks, indicating the necessity of developing lower-risk anti-melanogenic agents. Sugars are ubiquitous natural compounds found in humans and other organisms. Here, we review the recent advances in research on the roles of sugars and sugar-related agents in melanogenesis and in the development of sugar-based anti-melanogenic agents. The proposed mechanisms of action of these agents include: (a) (natural sugars) disturbing proper melanosome maturation by inducing osmotic stress and inhibiting the PI3 kinase pathway and (b) (sugar derivatives) inhibiting tyrosinase maturation by blocking N-glycosylation. Finally, we propose an alternative strategy for developing anti-melanogenic sugars that theoretically reduce melanosomal pH by inhibiting a sucrose transporter and reduce tyrosinase activity by inhibiting copper incorporation into an active site. These studies provide evidence of the utility of sugar-based anti-melanogenic agents in managing skin darkness and curing pigmentary disorders and suggest a future direction for the development of physiologically favorable anti-melanogenic agents.
Rifampicin Repurposing Reveals Anti-Melanogenic Activity in B16F10 Melanoma Cells.
Lee Y, Hyun C Molecules. 2025; 30(4).
PMID: 40005210 PMC: 11858211. DOI: 10.3390/molecules30040900.
Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery.
Brito S, Baek M, Bin B Pharmaceutics. 2024; 16(11).
PMID: 39598527 PMC: 11597055. DOI: 10.3390/pharmaceutics16111403.
Li R, Wang Y, Liu Y, Li D, Tian Y, Liu X Animals (Basel). 2023; 13(16).
PMID: 37627399 PMC: 10451703. DOI: 10.3390/ani13162608.
Sangkaew O, Prombutara P, Roytrakul S, Yompakdee C Microbiol Spectr. 2023; :e0313922.
PMID: 36861996 PMC: 10100879. DOI: 10.1128/spectrum.03139-22.
Kim H, Hyun C Molecules. 2023; 28(1).
PMID: 36615308 PMC: 9822252. DOI: 10.3390/molecules28010115.