采用纳米技术和生物工程方法,提高间充质干细胞作为现成的多功能肿瘤递送载体的效力。

IF 10.9 1区 医学 Q1 CHEMISTRY, MEDICINAL
Mojtaba Taheri, Hossein Abdul Tehrani, Sadegh Dehghani, Mona Alibolandi, Ehsan Arefian, Mohammad Ramezani
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引用次数: 0

摘要

在癌基因驱动的癌症中靶向可操作的突变以及免疫肿瘤学的发展是影响癌症治疗模式并导致精准肿瘤学出现的两大革命。然而,肿瘤间和肿瘤内异质性是这两个癌症精准治疗领域面临的主要挑战。换句话说,在特定类型的癌症患者中找到一种通用的标志物或途径具有挑战性。因此,针对单一标志物或途径的单一靶向疗法无法有效对抗肿瘤异质性。间充质干细胞(MSCs)具有细胞疗法的有利特性,包括低免疫性、固有的肿瘤趋向性、直接分离和多线分化潜力。间充质干细胞可装载各种化疗药物和溶瘤病毒。这些固有特性与遗传操作的可能性相结合,使间叶干细胞成为一种多功能肿瘤递送载体,可用于体内选择性肿瘤递送各种化疗和生物治疗药物。间充质干细胞可用作生物工厂,在肿瘤部位局部生产化学或生物抗癌剂。间充质干细胞介导的免疫疗法可促进免疫治疗药物在肿瘤部位的特异性持续释放,并可达到治疗浓度,而无需重复全身给药的高治疗剂量。尽管将间叶干细胞用于各种癌症治疗方法的临床前研究唤起了人们的热情,但将间叶干细胞转化为临床应用却面临着严峻的挑战。本手稿以批判的视角回顾了临床前和临床研究,这些研究评估了间充质干细胞作为一种选择性肿瘤递送工具在基因治疗、免疫治疗和化疗等各种癌症治疗方法中的应用。然后,讨论了可提高间充质干细胞肿瘤靶向效力的新型纳米技术和生物工程方法,以及克服间充质干细胞在肿瘤部位低定位相关挑战的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanotechnology and bioengineering approaches to improve the potency of mesenchymal stem cell as an off-the-shelf versatile tumor delivery vehicle

Targeting actionable mutations in oncogene-driven cancers and the evolution of immuno-oncology are the two prominent revolutions that have influenced cancer treatment paradigms and caused the emergence of precision oncology. However, intertumoral and intratumoral heterogeneity are the main challenges in both fields of precision cancer treatment. In other words, finding a universal marker or pathway in patients suffering from a particular type of cancer is challenging. Therefore, targeting a single hallmark or pathway with a single targeted therapeutic will not be efficient for fighting against tumor heterogeneity. Mesenchymal stem cells (MSCs) possess favorable characteristics for cellular therapy, including their hypoimmune nature, inherent tumor-tropism property, straightforward isolation, and multilineage differentiation potential. MSCs can be loaded with various chemotherapeutics and oncolytic viruses. The combination of these intrinsic features with the possibility of genetic manipulation makes them a versatile tumor delivery vehicle that can be used for in vivo selective tumor delivery of various chemotherapeutic and biological therapeutics. MSCs can be used as biofactory for the local production of chemical or biological anticancer agents at the tumor site. MSC-mediated immunotherapy could facilitate the sustained release of immunotherapeutic agents specifically at the tumor site, and allow for the achievement of therapeutic concentrations without the need for repetitive systemic administration of high therapeutic doses. Despite the enthusiasm evoked by preclinical studies that used MSC in various cancer therapy approaches, the translation of MSCs into clinical applications has faced serious challenges. This manuscript, with a critical viewpoint, reviewed the preclinical and clinical studies that have evaluated MSCs as a selective tumor delivery tool in various cancer therapy approaches, including gene therapy, immunotherapy, and chemotherapy. Then, the novel nanotechnology and bioengineering approaches that can improve the potency of MSC for tumor targeting and overcoming challenges related to their low localization at the tumor sites are discussed.

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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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