癌症治疗的革命:miRNA-34 的纳米制剂--增强各种癌症免疫疗法的传递和疗效:综述。

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Nanoscale Advances Pub Date : 2024-09-20 DOI:10.1039/D4NA00488D
Marola Paula Fawzy, Hatem A. F. M. Hassan, Nada K. Sedky, Mohamed S. Nafie, Rana A. Youness and Sherif Ashraf Fahmy
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引用次数: 0

摘要

尽管近来癌症疗法取得了进展,但仍存在严重的毒副作用、非选择性靶向、对化疗和放疗的耐药性以及转移性肿瘤复发等挑战。因此,人们一直在努力探索创新的抗癌化合物,特别是在免疫疗法方面,这些化合物有可能提高癌症预防和治疗的生物安全性和有效性。其中一个探索途径涉及 miRNA-34 (miR-34)家族,众所周知,该家族能够抑制各种癌症的肿瘤发生。在几种人类癌症中观察到了 miR-34 的失调,由于它与公认的肿瘤抑制因子 p53 的协同作用,它被认为是一种肿瘤抑制微 RNA。然而,miR-34a 的治疗应用也面临挑战。这些挑战包括 miR-34a 容易被血清中的 RNase 降解,从而限制了其穿透毛细血管内皮到达靶细胞的能力,以及免疫反应性不良反应的报道。此外,还可能出现意想不到的副作用,例如由于与纳米载体表面的血清蛋白相互作用,治疗用 miRNA 在健康组织中积聚;由于剪切应力,纳米粒子在血液中分解;由于间质压力,纳米载体不能成功外渗到靶细胞。尽管存在这些挑战,miR-34a 仍然是一种很有希望的癌症治疗候选药物,miR-34 家族的其他成员也显示出抑制肿瘤细胞增殖的潜力。虽然 miR-34b/c 在体内的应用有限,但它们在肿瘤治疗方面值得进一步探索。最近,人们开发了利用纳米颗粒的程序,以应对与 miR-34 临床应用相关的挑战,并在体外和体内显示出疗效。本综述重点介绍了用于靶向癌细胞的 miR-34 纳米给药系统的新趋势,深入探讨了旨在增强 miR-34 的抗癌治疗活性和靶向精确性的新型纳米制剂。据目前所知,近期还没有类似的综述全面论述旨在优化 miR-34 在抗癌策略中的治疗潜力的各种纳米制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Revolutionizing cancer therapy: nanoformulation of miRNA-34 – enhancing delivery and efficacy for various cancer immunotherapies: a review

Despite recent advancements in cancer therapies, challenges such as severe toxic effects, non-selective targeting, resistance to chemotherapy and radiotherapy, and recurrence of metastatic tumors persist. Consequently, there has been considerable effort to explore innovative anticancer compounds, particularly in immunotherapy, which offer the potential for enhanced biosafety and efficacy in cancer prevention and treatment. One such avenue of exploration involves the miRNA-34 (miR-34) family, known for its ability to inhibit tumorigenesis across various cancers. Dysregulation of miR-34 has been observed in several human cancers, and it is recognized as a tumor suppressor microRNA due to its synergistic interaction with the well-established tumor suppressor p53. However, challenges have arisen with the therapeutic application of miR-34a. These include its susceptibility to degradation by RNase in serum, limiting its ability to penetrate capillary endothelium and reach target cells, as well as reports of immunoreactive adverse reactions. Furthermore, unexpected side effects may occur, such as the accumulation of therapeutic miRNAs in healthy tissues due to interactions with serum proteins on nano-vector surfaces, nanoparticle breakdown in the bloodstream due to shearing stress, and unsuccessful extravasation of nanocarriers to target cells owing to interstitial fluid pressure. Despite these challenges, miR-34a remains a promising candidate for cancer therapy, and other members of the miR-34 family have also shown potential in inhibiting tumor cell proliferation. While the in vivo applications of miR-34b/c are limited, they warrant further exploration for oncotherapy. Recently, procedures utilizing nanoparticles have been developed to address the challenges associated with the clinical use of miR-34, demonstrating efficacy both in vitro and in vivo. This review highlights emerging trends in nanodelivery systems for miR-34 targeting cancer cells, offering insights into novel nanoformulations designed to enhance the anticancer therapeutic activity and targeting precision of miR-34. As far as current knowledge extends, no similar recent review comprehensively addresses the diverse nanoformulations aimed at optimizing the therapeutic potential of miR-34 in anticancer strategies.

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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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