乳铁蛋白作为靶向癌症的多功能大分子配体的研究进展

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Nidhi Sharma, Nousheen Khatoon, Mohammad Adnan Raza, Suprit Dilip Saoji, Dilpreet Singh
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引用次数: 0

摘要

本研究严格审查了乳铁蛋白(一种多功能铁螯合糖蛋白)作为精确癌症治疗的大分子配体的最新进展。该研究强调了乳铁蛋白的分子机制,基于纳米配方的新方法,及其克服精确肿瘤学固有的治疗局限性的协同潜力。乳铁蛋白存在于牛奶和粘膜分泌物中,具有很强的抗肿瘤、抗炎和免疫调节活性。乳铁蛋白与癌细胞特异性受体(如转铁蛋白和低密度脂蛋白受体相关蛋白)具有高亲和力结合,允许选择性靶向和内化,并限制脱靶毒性。乳铁蛋白调节PI3K/Akt和MAPK等致癌途径,有效抑制肿瘤生长和转移。通过脂质体和聚合纳米颗粒等纳米制剂,增强了药代动力学特征,并使药物释放以肿瘤为导向,从而提高了传统化疗药物的疗效。乳铁蛋白通过受体介导的胞吞作用穿透血脑屏障等生物屏障,为治疗胶质母细胞瘤等难治性癌症提供了新的平台。此外,其免疫调节作用,如NK细胞和巨噬细胞极化到M1表型的激活,分别增强抗肿瘤免疫,补充免疫治疗方法。本研究还详细阐述了乳铁蛋白通过调节p -糖蛋白等外排泵在克服多药耐药中的作用。该综述全面整合了分子、临床前和临床特征,强调了乳铁蛋白在精密肿瘤学中的革命性潜力,其先进的纳米配方和协同免疫调节活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A pioneer review on lactoferrin as versatile macromolecular ligand for targeting cancer: recent advances.

This review critically evaluates the emerging role of lactoferrin, an iron-chelating glycoprotein, as a macromolecular ligand in precision cancer therapy. Lactoferrin exhibits potent anti-tumour, anti-inflammatory, and immunomodulatory properties and targets cancer cells via high-affinity binding to transferrin and LDL receptor-related proteins, enhancing selectivity and minimizing off-target toxicity. It modulates key oncogenic pathways such as PI3K/Akt and MAPK to suppress tumour growth and metastasis. Nanoformulations-like liposomes and polymeric nanoparticles-improve pharmacokinetics, enable targeted drug delivery, and enhance therapeutic efficacy. Lactoferrin's ability to cross biological barriers, including the blood-brain barrier via receptor-mediated transcytosis, offers promise for treating difficult cancers such as glioblastoma. Additionally, it enhances anti-tumour immunity by activating NK cells and polarizing macrophages to the M1 phenotype. Importantly, lactoferrin helps overcome multidrug resistance by modulating efflux pumps like P-glycoprotein. Integrating molecular insights with preclinical and clinical evidence, this review underscores lactoferrin's transformative potential in precision oncology through advanced nanoformulations and synergistic immunomodulatory mechanisms.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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