College of Life Science, Henan Normal University, Xinxiang, 453007, Henan, China.
Department of Biology, East Carolina University, Greenville, NC, 27858, USA.
Funct Integr Genomics. 2023 May 26;23(2):182. doi: 10.1007/s10142-023-01117-w.
Cancer is one of the leading causes of death worldwide and it has the trend of increase incidence. However, in the past decades, as quickly developed new technologies and modified old techniques for cancer screening, diagnosis, and treatment, the cancer-caused mortality rates dropped quickly, and the survival times of cancer patients are enhanced. However, the current death rate is still about 50% and the survival patients always suffer from the side effect of current cancer treatments. Recently developed Nobel Prize-winning CRISPR/Cas technology provides new hope on cancer screening, early diagnosis, and clinic treatment as well as new drug development. Currently, four major CRISPR/Cas9-derived genome editors, CRISPR/Cas9 nucleotide sequence editor, CRISPR/Cas base editor (BE), CRISPR prime editor (PE), and CRISPR interference (CRISPRi) (including both CRISPRa and CRISPRr), were well developed and used to various research and applications, including cancer biology study and cancer screening, diagnosis, and treatment. Additionally, CRISPR/Cas12 and CRISPR/Cas13 genome editors were also widely used in cancer-related basic and applied research as well as treatment. Cancer-associated SNPs and genetic mutations as well as both oncogenes and tumor suppressor genes are perfect targets for CRISPR/Cas-based gene therapy for cancer treatment. CRISPR/Cas is also employed to modify and generate new Chimeric antigen receptor (CAR) T-cells for improving its safety, efficiency, and longer-time last for treating various cancers. Currently, there are many clinic trails of CRISPR-based gene therapy for cancer treatments. Although all CRISPR/Cas-derived genome and epigenome tools are promising methods for cancer biology study and treatment, the efficiency and long term-safety are still the major concerns for CRISPR-based gene therapy. Developing new CRISPR/Cas delivery methods and reducing the potential side effects, including off-target impacts, will enhance CRISPR/Cas application in cancer-related research, diagnosis, and therapeutical treatment.
癌症是全球主要死因之一,且其发病率呈上升趋势。然而,在过去几十年中,随着癌症筛查、诊断和治疗新技术的快速发展和旧技术的改进,癌症死亡率迅速下降,癌症患者的生存时间得到延长。然而,目前的死亡率仍约为 50%,且生存患者常遭受当前癌症治疗的副作用之苦。最近开发的诺贝尔获奖技术 CRISPR/Cas 为癌症筛查、早期诊断和临床治疗以及新药开发提供了新的希望。目前,四大 CRISPR/Cas9 衍生基因组编辑器,即 CRISPR/Cas9 核苷酸序列编辑器、CRISPR/Cas 碱基编辑器(BE)、CRISPR 先导编辑器(PE)和 CRISPR 干扰(CRISPRi)(包括 CRISPRa 和 CRISPRr),已得到很好的开发和应用,用于包括癌症生物学研究和癌症筛查、诊断和治疗在内的各种研究和应用。此外,CRISPR/Cas12 和 CRISPR/Cas13 基因组编辑器也广泛应用于癌症相关的基础和应用研究以及治疗。癌症相关的单核苷酸多态性和遗传突变以及癌基因和肿瘤抑制基因都是基于 CRISPR 的癌症治疗基因治疗的完美靶点。CRISPR/Cas 还用于修饰和产生新的嵌合抗原受体(CAR)T 细胞,以提高其安全性、效率和更长时间的治疗各种癌症的效果。目前,有许多基于 CRISPR 的基因治疗癌症的临床试验。虽然所有基于 CRISPR 的基因组和表观基因组工具都是癌症生物学研究和治疗的有前途的方法,但效率和长期安全性仍然是基于 CRISPR 的基因治疗的主要关注点。开发新的 CRISPR/Cas 递药方法并降低潜在的副作用,包括脱靶效应,将增强 CRISPR/Cas 在癌症相关研究、诊断和治疗中的应用。