crispr / cas9基因编辑在癌症治疗中的前景与挑战:文献综述

D. Abdussadyk, A. Beisenova
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引用次数: 0

摘要

相关性:癌症仍然是哈萨克斯坦人死亡的主要原因之一,CRISPR/Cas9为治疗癌症提供了可能的解决方案。聚集的、有规律间隔的短回文重复序列/CRISPR相关蛋白9 (CRISPR/Cas9)是细菌用来切割外来入侵者的系统。该系统允许研究人员编辑癌细胞基因,因此被认为有望用于癌症治疗。该系统需要更多的试验,因此必须提高学生和潜在投资者对该技术的认识,并强调当前的挑战可能是研究人员的研究机会。该研究旨在分析和提供来自知名科学期刊的关于当前CRISPR/Cas9系统在癌症治疗中的使用的最新信息,供医学生和研究人员使用。这篇研究论文还强调了在癌症治疗的临床环境中实施CRISPR/Cas9所面临的挑战。方法:检索科学文献和数据库(PubMed和Nature Journal),分析CRISPR/Cas9系统在癌症治疗中的应用。结果:本研究结果表明,科学家应致力于改进Cas蛋白的类型和结构以及递送方法,包括非病毒递送方法(脂质体颗粒,杂交载体,金纳米颗粒和细胞外囊泡),以改善癌症治疗的现状。结论:CRISPR/Cas9是一项仍然充满挑战的重要技术,应该转化为研究机会。目前的挑战包括Cas核酸酶的形式和结构、工程的类型(体内与体外)以及递送方法的多样性。每种交付方式都有优缺点,需要进一步研究。特别是,未来的研究应集中在非病毒载体上,如脂质体基颗粒、细胞外囊泡、杂交囊泡和金纳米颗粒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE PROSPECTS AND CHALLENGES OF CRISPR/CAS9 GENE EDITING IN CANCER THERAPY: A LITERATURE REVIEW
Relevance: Cancer remains one of the leading causes of death in Kazakhstan, and CRISPR/Cas9 offers possible solutions to treat it. Clustered, regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9) is a system bacteria use to cleave foreign in-vaders. This system has been considered promising for cancer therapeutics by allowing researchers to edit cancer cell genes. The system requires more trials, so it is essential to raise awareness of this technique for stu-dents and potential investors and highlight the current challenges that could be research opportuni-ties for researchers. The study aimed to analyze and provide up-to-date information from reputable scientific journals on the current use of the CRISPR/Cas9 system in cancer therapeutics for medical students and researchers. This research paper also highlights the challenges associated with implementing CRISPR/Cas9 in clinical settings for cancer therapeutics. Methods: The scientific literature and databases (PubMed and the Nature Journal) were searched and analyzed using the CRISPR/Cas9 system in cancer therapy. Results: The results of this research indicate that scientists should focus on improving the types and structure of the Cas protein as well as the delivery methods, including the non-viral deliv-ery methods (liposome-based particles, hybrid vectors, gold nanoparticles, and extracellular vesicles) to contribute to improving the current status of cancer therapeutics. Conclusion: CRISPR/Cas9 is an important technique that is still fraught with challenges and should be turned into research opportunities. The current challenges include the form and structure of the Cas nuclease, the types of engineering (in vivo vs. ex vivo), and the varieties of delivery methods. Each delivery method type has pros and cons and requires further research. In particular, future studies should focus on non-viral vectors, such as liposome-based particles, extracellular vesi-cles, hybrid vesicles, and gold nanoparticles.
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