A pioneer review on lactoferrin as versatile macromolecular ligand for targeting cancer: recent advances

Authors:
Publisher website
Google Scholar
Abstract
This study critically examines recent developments in the use of lactoferrin, a multi-functional iron-chelating glycoprotein, as a macromolecular ligand for precision cancer therapy. The study highlights the molecular mechanism of lactoferrin, nano-formulation based novel approaches, and its synergistic potential to surmount therapeutic limitations inherent to precision oncology. Lactoferrin, found in milk and mucosal secretions, exhibits intense anti-tumor, anti-inflammatory, and immunomodulatory activities. Lactoferrin binds with high affinity to cancer cell-specific receptors, such as transferrin and low-density lipoprotein receptor-related proteins, allowing for selective targeting and internalization and limiting off-target toxicity. Lactoferrin modulates oncogenic pathways like PI3K/Akt and MAPK, and potently inhibits tumor growth and metastasis. Pharmacokinetic profiles are enhanced and drug release is made tumor-directed by nanoformulations such as liposomes and polymeric nanoparticles, respectively, enhancing the efficacy of conventional chemotherapeutics. Lactoferrin penetration of biological barriers like the blood-brain barrier by receptor-mediated transcytosis offers new platforms for therapy of intractable cancers such as glioblastoma. Moreover, its immunomodulatory effects, such as the activation of NK cells and macrophage polarization to an M1 phenotype, enhance anti-tumor immunity, respectively, complementing immunotherapeutic approaches. The study also elaborates on the roles of lactoferrin in overcoming multidrug resistance through the modulation of efflux pumps like P-glycoprotein. The review thoroughly integrates molecular, preclinical, and clinical characteristics, highlighting lactoferrin's revolutionary potential in precision oncology by advanced nano formulations and synergistic immunomodulatory activity.

This publication has 142 references indexed in Scilit: