Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, South Africa.
Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, South Africa.
Biomed Pharmacother. 2024 Nov;180:117516. doi: 10.1016/j.biopha.2024.117516. Epub 2024 Sep 26.
CRISPR/Cas9 precision genome editing has revolutionized cancer treatment by introducing specific alterations to the cancer genome. But the therapeutic potential of CRISPR/Cas9 is limited by off-target effects, which can cause undesired changes to genomic regions and create major safety concerns. The primary emphasis lies in their implications within the realm of cancer photodynamic therapy (PDT), where precision is paramount. PDT is a promising cancer treatment method; nevertheless, its effectiveness is severely limited and readily leads to recurrence due to the therapeutic resistance of cancer stem cells (CSCs). With a focus on targeted genome editing into cancer cells during PDT and stem cell treatment (SCT), the review aims to further the ongoing search for safer and more accurate CRISPR/Cas9-mediated methods. At the core of this exploration are recent advancements and novel techniques that offer promise in mitigating the risks associated with off-target effects. With a focus on cancer PDT and SCT, this review critically assesses the landscape of off-target effects in CRISPR/Cas9 applications, offering a comprehensive knowledge of their nature and prevalence. A key component of the review is the assessment of cutting-edge delivery methods, such as technologies based on nanoparticles (NPs), to optimize the distribution of CRISPR components. Additionally, the study delves into the intricacies of guide RNA design, focusing on advancements that bolster specificity and minimize off-target effects, crucial elements in ensuring the precision required for effective cancer PDT and SCT. By synthesizing insights from various methodologies, including the exploration of innovative genome editing tools and leveraging robust validation methods and bioinformatics tools, the review aspires to chart a course towards more reliable and precise CRISPR-Cas9 applications in cancer PDT and SCT. For safe PDT and SCT integration in cancer therapy, CRISPR/Cas9 precision optimization is essential. Utilizing sophisticated molecular and computational techniques to address off-target effects is crucial to realizing the therapeutic promise of these technologies, which will ultimately lead to the development of individualized and successful cancer treatment strategies. Our long-term goals are to improve precision genome editing for more potent cancer therapy approaches by refining the way CRISPR/Cas9 is integrated with photodynamic and stem cell therapies.
CRISPR/Cas9 精确基因组编辑通过引入对癌症基因组的特定改变,彻底改变了癌症治疗。但 CRISPR/Cas9 的治疗潜力受到脱靶效应的限制,这些效应会导致基因组区域的非预期改变,并引发重大安全问题。主要重点在于其在癌症光动力疗法 (PDT) 中的应用,在该领域,精确至关重要。PDT 是一种有前途的癌症治疗方法;然而,由于癌症干细胞 (CSC) 的治疗抵抗,其有效性受到严重限制,并且容易导致复发。本综述重点关注 PDT 和干细胞治疗 (SCT) 期间靶向基因组编辑到癌细胞,旨在进一步寻找更安全、更准确的 CRISPR/Cas9 介导方法。这一探索的核心是最近的进展和新技术,这些技术为减轻脱靶效应相关风险提供了希望。本综述重点关注癌症 PDT 和 SCT,批判性地评估了 CRISPR/Cas9 应用中的脱靶效应,全面了解其性质和普遍性。综述的一个关键组成部分是评估前沿的递药方法,例如基于纳米颗粒 (NPs) 的技术,以优化 CRISPR 组件的分布。此外,该研究深入探讨了向导 RNA 设计的复杂性,重点介绍了提高特异性和最小化脱靶效应的进展,这是确保有效癌症 PDT 和 SCT 所需的精确性的关键因素。通过综合各种方法学的见解,包括探索创新的基因组编辑工具以及利用强大的验证方法和生物信息学工具,本综述旨在为癌症 PDT 和 SCT 中更可靠和精确的 CRISPR-Cas9 应用指明方向。为了实现安全的 PDT 和 SCT 与癌症治疗的整合,CRISPR/Cas9 精确优化至关重要。利用复杂的分子和计算技术来解决脱靶效应是实现这些技术治疗潜力的关键,这最终将导致个体化和成功的癌症治疗策略的发展。我们的长期目标是通过改进 CRISPR/Cas9 与光动力和干细胞疗法的整合方式,来提高精确基因组编辑,以实现更有效的癌症治疗方法。