Department of Health Management, Shengjing Hospital of China Medical University, Shenyang, 110004, P. R. China.
Department of General Surgery, Shengjing Hospital of China Medical University, 36 Sanhao Street, Heping District, Shenyang, 110004, Liaoning Province, P. R. China.
Cell Biol Toxicol. 2024 Nov 20;40(1):101. doi: 10.1007/s10565-024-09943-9.
Gastric cancer (GC) is the fifth most common cancer worldwide, particularly prevalent in Asia, especially in China, where both its incidence and mortality rates are significantly high. Meanwhile, nanotechnology has demonstrated great potential in the treatment of GC. In particular, nanodrug delivery systems have improved therapeutic efficacy and targeting through various functional modifications, such as targeting peptides, tumor microenvironment responsiveness, and instrument-based methods. For instance, silica (SiO) has excellent biocompatibility and can be used as a drug carrier, with its porous structure enhancing drug loading capacity. Polymer nanoparticles regulate drug release rates and mechanisms by altering material composition and preparation methods. Lipid nanoparticles efficiently encapsulate hydrophilic drugs and promote cellular uptake, while carbon-based nanoparticles can be used in biosensors and drug delivery. Targets such as integrins, HER2 receptors, and the tumor microenvironment have been used to improve drug efficacy in GC treatment. Nanodrug delivery techniques not only enhance drug efficacy and delivery capabilities but also selectively target tumor cells. Currently, there is a lack of systematic summarization and synthesis regarding the relationship between nanodrug delivery systems and GC treatment, which to some extent hinders researchers and clinicians from efficiently searching for and referencing related studies, thereby reducing work efficiency. This study aims to systematically summarize the existing research on the relationship between nanodrug delivery systems and GC treatment, making it easier for professionals to search and reference, and thereby promoting further research on the role of nanodrug delivery systems and their clinical applications in GC. This review discusses the applications of functionalized nanocarriers in the treatment of GC in recent years, including surface modifications with targeted markers, the combination of phototherapy, chemotherapy, and immunotherapy, along with their advantages and challenges. It also examines the future prospects of targeted nanomaterials in GC treatment. The review particularly focuses on the combined application of nanocarriers in multiple treatment modalities, such as phototherapy, chemotherapy, and immunotherapy, demonstrating their potential in multimodal treatments. Furthermore, it thoroughly explores the specific challenges that nanocarriers face in GC treatment, such as biocompatibility, drug release control, and clinical translation issues, while providing a systematic outlook on future developments. Additionally, this study emphasizes the potential value and feasibility of nanocarriers in clinical applications, contrasting with most reviews that focus on basic research. Through these innovations, we offer new perspectives and directions for the development of nanotechnology in the treatment of GC.
胃癌(GC)是全球第五大常见癌症,尤其在亚洲流行,尤其是在中国,其发病率和死亡率都很高。同时,纳米技术在胃癌的治疗中显示出巨大的潜力。特别是,纳米药物递送系统通过各种功能修饰,如靶向肽、肿瘤微环境响应性和基于仪器的方法,提高了治疗效果和靶向性。例如,二氧化硅(SiO)具有极好的生物相容性,可以用作药物载体,其多孔结构提高了药物载药量。聚合物纳米粒子通过改变材料组成和制备方法来调节药物释放速率和机制。脂质纳米粒子有效地包封亲水性药物并促进细胞摄取,而基于碳的纳米粒子可用于生物传感器和药物递送。整合素、HER2 受体和肿瘤微环境等靶标已被用于提高 GC 治疗中的药物疗效。纳米药物递送技术不仅增强了药物的疗效和递送能力,而且还选择性地靶向肿瘤细胞。目前,关于纳米药物递送系统与 GC 治疗之间的关系缺乏系统的总结和综合,在某种程度上阻碍了研究人员和临床医生高效地搜索和参考相关研究,从而降低了工作效率。本研究旨在系统地总结纳米药物递送系统与 GC 治疗之间的现有研究,使专业人员更容易搜索和参考,从而促进纳米药物递送系统的作用及其在 GC 中的临床应用的进一步研究。本综述讨论了近年来功能化纳米载体在 GC 治疗中的应用,包括靶向标记物的表面修饰、光疗、化疗和免疫治疗的结合,以及它们的优点和挑战。还研究了靶向纳米材料在 GC 治疗中的未来前景。该综述特别关注纳米载体在多种治疗方式中的联合应用,如光疗、化疗和免疫治疗,展示了它们在多模态治疗中的潜力。此外,它还深入探讨了纳米载体在 GC 治疗中面临的具体挑战,如生物相容性、药物释放控制和临床转化问题,同时对未来发展进行了系统展望。此外,本研究强调了纳米载体在临床应用中的潜在价值和可行性,与大多数关注基础研究的综述形成对比。通过这些创新,我们为纳米技术在 GC 治疗中的发展提供了新的视角和方向。
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