Molecular Pathway Modulation and Nanotechnology‐Based Therapeutic Strategies for Shikonin

纳米载体 药理学 化学 免疫疗法 药物输送 免疫系统 体内 细胞周期检查点 癌症研究 信号转导 细胞 细胞毒性 适体 医学 癌细胞 细胞周期 生物相容性 固体脂质纳米粒 癌症免疫疗法 细胞信号 纳米医学
作者
Haibo Wang,Qiwei Tian,Lu Yang,Shengzhe Huang,Gang Wang,Xin Yuan,Panbo Zhang,Hui Liu,Gang Huang,Hao Yang
出处
期刊:Advanced Healthcare Materials [Wiley]
卷期号:: e03750-e03750
标识
DOI:10.1002/adhm.202503750
摘要

ABSTRACT Chinese herbal medicine Radix lithospermi (Lithospermum erythrorhizon), a traditional medicinal herb widely utilized in China, yields Shikonin as a bioactive monomeric compound. Shikonin demonstrates multifaceted pharmacological profiles, encompassing analgesic, anti‐inflammatory, antineoplastic, and hemostatic activities. Notably, Shikonin has demonstrated significant inhibitory activity against a variety of malignancies, particularly offering promising strategies for addressing Nano‐based strategy, Pyruvate kinase M2 (PKM2), shikonin, tumor metabolism, and drug‐resistant cancers. This review systematically synthesizes the latest advancements in Shikonin's anti‐cancer efficacy, providing a theoretical foundation and future directions for its mechanisms, clinical applications, and nano‐based treatment optimizations. Shikonin acts as a selective PKM2 inhibitory agent, modulating tumor metabolism and regulating critical signaling pathways to mediate its antitumor activity. Shikonin exerts anticarcinogenic effects through suppressing neoplastic cell growth, triggering programmed cell death, halting cell cycle progression, enhancing autophagic activity, and inhibiting metastatic dissemination. However, the targetability, cellular permeability, and in vivo safety of Shikonin are critical limitations restricting its clinical application. Therefore, nano‐based therapeutic strategies involving Shikonin, where it is integrated with nanoparticles, nanocarriers, nanoliposomes, and other nanomaterials to enhance immunotherapy and targeted therapy outcomes. To address the current limitations, modifying nanocarriers with chemical groups, antibodies, peptides, or aptamers can improve the precision of tumor‐specific delivery of Shikonin. Bioengineered cell‐derived nanoscale vesicles for Shikonin delivery can enhance biocompatibility and reduce the risk of immune rejection. However, due to the inherent toxicity of Shikonin itself and its pharmacokinetic properties, the use of nano‐materials for its delivery is crucial. Nevertheless, the application of nano‐therapy with Shikonin is still at the stage of cellular and animal experiments. Extensive preclinical research is needed to evaluate the combination of Shikonin with advanced treatment modalities to determine the optimal synergistic effects and avoid adverse interactions. Due to the lack of clinical studies, enhancing clinical research on nano‐therapy will be a key focus for future research.
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