披着羊皮的狼:用人血清白蛋白驯服癌症的耐药性?

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-03-19 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S500997
Iga Stukan, Anna Żuk, Kamila Pukacka, Julia Mierzejewska, Jakub Pawłowski, Bogusław Kowalski, Maria Dąbkowska
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引用次数: 0

摘要

人血清白蛋白(HSA)已成为一种很有前途的纳米药物载体,它具有独特的结构特性,可以克服癌症治疗中的关键挑战,特别是对化疗的耐药性。本文综述了基于白蛋白的纳米颗粒的细胞摄取,以及通过改善对癌细胞的靶向,增强其绕过耐药机制的能力的修饰,特别是多药耐药1型(MDR1)。在我们独特的方法中,我们整合了白蛋白的化学性质,它与癌细胞的相互作用,以及基于白蛋白的递送系统的表面修饰,这些系统能够绕过耐药机制,特别是与MDR1相关的机制,并精确地靶向癌细胞上的受体,以提高治疗效果。我们讨论了虽然成熟的白蛋白受体如gp60和gp18/30对细胞摄取和胞吞作用至关重要,但它们的生物学仍未被充分探索,限制了它们的翻译潜力。此外,我们还探索了新兴靶点的潜力,如分化簇44 (CD44)、分化簇(CD36)和转铁蛋白受体TfR1,以及使用二聚体形式的白蛋白(dHSA)进一步增强对耐药癌细胞的递送的优势。根据临床实例,包括白蛋白结合紫杉醇(Abraxane)的成功和新配方,如Pazenir和Fyarro(用于西罗莫司),我们确定了当前知识的空白,并提出了优化白蛋白系统的策略。总之,基于白蛋白的纳米颗粒,如果经过适当的修饰,有可能绕过多药耐药性,提高对癌细胞的靶向性。通过增强白蛋白有效递送治疗药物的能力,这些载体代表了解决肿瘤学最持久挑战之一的有希望的方法,具有改善癌症治疗结果的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Wolf in Sheep's Clothing: Taming Cancer's Resistance with Human Serum Albumin?

Human serum albumin (HSA) has emerged as a promising carrier for nanodrug delivery, offering unique structural properties that can be engineered to overcome key challenges in cancer treatment, especially resistance to chemotherapy. This review focuses on the cellular uptake of albumin-based nanoparticles and the modifications that enhance their ability to bypass resistance mechanisms, particularly multidrug resistance type 1 (MDR1), by improving targeting to cancer cells. In our unique approach, we integrate the chemical properties of albumin, its interactions with cancer cells, and surface modifications of albumin-based delivery systems that enable to bypass resistance mechanisms, particularly those related to MDR1, and precisely target receptors on cancer cells to improve treatment efficacy. We discuss that while well-established albumin receptors such as gp60 and gp18/30 are crucial for cellular uptake and transcytosis, their biology remains underexplored, limiting their translational potential. Additionally, we explore the potential of emerging targets, such as cluster of differentiation 44 (CD44), cluster of differentiation (CD36) and transferrin receptor TfR1, as well as the advantages of using dimeric forms of albumin (dHSA) to further enhance delivery to resistant cancer cells. Drawing from clinical examples, including the success of albumin-bound paclitaxel (Abraxane) and new formulations like Pazenir and Fyarro (for Sirolimus), we identify gaps in current knowledge and propose strategies to optimize albumin-based systems. In conclusion, albumin-based nanoparticles, when tailored with appropriate modifications, have the potential to bypass multidrug resistance and improve the targeting of cancer cells. By enhancing albumin's ability to efficiently deliver therapeutic agents, these carriers represent a promising approach to addressing one of oncology's most persistent challenges, with substantial potential to improve cancer treatment outcomes.

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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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