State of the art CRISPR-based strategies for cancer diagnostics and treatment.

IF 9.5 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Emma Di Carlo, Carlo Sorrentino
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引用次数: 0

Abstract

Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology is a groundbreaking and dynamic molecular tool for DNA and RNA "surgery". CRISPR/Cas9 is the most widely applied system in oncology research. It is a major advancement in genome manipulation due to its precision, efficiency, scalability and versatility compared to previous gene editing methods. It has shown great potential not only in the targeting of oncogenes or genes coding for immune checkpoint molecules, and in engineering T cells, but also in targeting epigenomic disturbances, which contribute to cancer development and progression. It has proven useful for detecting genetic mutations, enabling the large-scale screening of genes involved in tumor onset, progression and drug resistance, and in speeding up the development of highly targeted therapies tailored to the genetic and immunological profiles of the patient's tumor. Furthermore, the recently discovered Cas12 and Cas13 systems have expanded Cas9-based editing applications, providing new opportunities in the diagnosis and treatment of cancer. In addition to traditional cis-cleavage, they exhibit trans-cleavage activity, which enables their use as sensitive and specific diagnostic tools. Diagnostic platforms like DETECTR, which employs the Cas12 enzyme, that cuts single-stranded DNA reporters, and SHERLOCK, which uses Cas12, or Cas13, that specifically target and cleave single-stranded RNA, can be exploited to speed up and advance oncological diagnostics. Overall, CRISPR platform has the great potential to improve molecular diagnostics and the functionality and safety of engineered cellular medicines. Here, we will emphasize the potentially transformative impact of CRISPR technology in the field of oncology compared to traditional treatments, diagnostic and prognostic approaches, and highlight the opportunities and challenges raised by using the newly introduced CRISPR-based systems for cancer diagnosis and therapy.

基于crispr的癌症诊断和治疗策略的最新进展。
聚类规则间隔短回文重复序列(CRISPR)技术是DNA和RNA“手术”的突破性动态分子工具。CRISPR/Cas9是肿瘤研究中应用最广泛的系统。与以前的基因编辑方法相比,它具有精度、效率、可扩展性和多功能性,是基因组操作的重大进步。它不仅在靶向癌基因或编码免疫检查点分子的基因、工程T细胞方面显示出巨大的潜力,而且在靶向有助于癌症发生和进展的表观基因组紊乱方面也显示出巨大的潜力。事实证明,它有助于检测基因突变,能够大规模筛选与肿瘤发病、进展和耐药性有关的基因,并加快针对患者肿瘤的遗传和免疫特征量身定制的高度靶向治疗的开发。此外,最近发现的Cas12和Cas13系统扩展了基于cas9的编辑应用,为癌症的诊断和治疗提供了新的机会。除了传统的顺式切割外,它们还具有反式切割活性,这使它们能够作为敏感和特定的诊断工具使用。像DETECTR这样的诊断平台,使用Cas12酶来切割单链DNA报告,SHERLOCK使用Cas12或Cas13,专门靶向和切割单链RNA,可以用来加快和推进肿瘤诊断。总的来说,CRISPR平台在提高分子诊断和工程细胞药物的功能和安全性方面具有巨大的潜力。在这里,我们将强调与传统治疗、诊断和预后方法相比,CRISPR技术在肿瘤领域的潜在变革性影响,并强调使用新引入的基于CRISPR的癌症诊断和治疗系统所带来的机遇和挑战。
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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来源期刊
Biomarker Research
Biomarker Research Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
15.80
自引率
1.80%
发文量
80
审稿时长
10 weeks
期刊介绍: Biomarker Research, an open-access, peer-reviewed journal, covers all aspects of biomarker investigation. It seeks to publish original discoveries, novel concepts, commentaries, and reviews across various biomedical disciplines. The field of biomarker research has progressed significantly with the rise of personalized medicine and individual health. Biomarkers play a crucial role in drug discovery and development, as well as in disease diagnosis, treatment, prognosis, and prevention, particularly in the genome era.
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