2. Academic Validation
  3. Glycosylation on breast cancer cell surface promotes the internalization and enhances therapeutic efficacy of cationic antimicrobial peptide L-K6

Glycosylation on breast cancer cell surface promotes the internalization and enhances therapeutic efficacy of cationic antimicrobial peptide L-K6

  • Toxicol Appl Pharmacol. 2025 Oct:503:117481. doi: 10.1016/j.taap.2025.117481.
Bo Wang 1,  Yiwei Zhao 2,  Qiuju Zhang 2,  Jiaqi Zhao 2,  Che Wang 3,  Dejing Shang 4
Affiliations

Affiliations

  • 1 Department of Medicinal Chemistry, School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China; Ningde Senior High School, Ningde 352101, China.
  • 2 Department of Medicinal Chemistry, School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China.
  • 3 Department of Medicinal Chemistry, School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian 116029, China; Liaoning Provincial Key Laboratory of Biotechnology and Drug Discovery, Liaoning Normal University, Dalian 116081, China. Electronic address: wangche126@lnnu.edu.cn.
  • 4 Liaoning Provincial Key Laboratory of Biotechnology and Drug Discovery, Liaoning Normal University, Dalian 116081, China; School of Life Science, Liaoning Normal University, Dalian 116081, China. Electronic address: djshang@lnnu.edu.cn.
PMID: 40684813 DOI: 10.1016/j.taap.2025.117481
Abstract

Cationic antimicrobial peptides (CAPs) have demonstrated Anticancer activity, which is thought to arise from interactions with negatively charged molecules on Cancer cell membranes. However, the precise cellular and molecular mechanisms underlying this process remain unclear. In this study, we investigated the role of negatively charged glycosylated molecules, located on the cell surface and endosomal membranes, in the internalization and Anticancer activity of L-K6, a synthetic lysine/leucine-rich CAP, using three human breast Cancer cell lines. Our findings revealed that sialic acid on cell membrane critically impacts L-K6's binding and internalization. Specifically, monosialotetrahexosylganglioside (GM1) and O-glycosylated Mucin-1 (bearing sialic acid) promoted L-K6 entry via caveolae-mediated endocytosis and macropinocytosis, whereas N-glycoproteins inhibited uptake. Furthermore, sialic acid on endosomal membranes enhanced L-K6 escape from endosomes, preventing intracellular degradation and enabling cytotoxic activity. Collectively, our results demonstrate that glycosylated molecules on breast Cancer cells regulate L-K6 internalization and cytotoxicity, providing a foundation for developing novel peptide-based Anticancer therapies targeting cell surface glycosylation.

Keywords

Breast cancer; Cationic antimicrobial peptide; Cell surface glycosylation; Endosome escape.

Figures
Products