Noormohamadi Hanieh, Soleimani Samarkhazan Hamed, Kargar Maryam, Maroufi Faezeh, Servatian Nazli, Davami Fatemeh
Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Malaria and Vector Research Group, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Discov Oncol. 2025 Aug 11;16(1):1530. doi: 10.1007/s12672-025-03383-5.
Pancreatic cancer is marked by a poor prognosis and an exceptionally high mortality rate, with its aggressive nature contributing to its classification as a highly malignant disease. For effective therapeutic strategies, the development of sophisticated and regulated DNA manipulation methods is essential. Originally part of the prokaryotic immune system, CRISPR/Cas has emerged as a pivotal genome-editing tool with promising applications in pancreatic cancer research and therapy. This gene editing method is known for simplicity, rapid advancement, and superior precision compared to earlier techniques. Its adaptability allows precise gene editing for therapeutic purposes, including oncogene silencing and correction of pathogenic mutations. Additionally, CRISPR-driven gene editing has facilitated the development of pancreatic cancer models, which serve as valuable platforms for drug discovery and personalized treatment strategies, offering deeper insights into the genetic landscape of pancreatic tumors. This article provides an overview of the current applications of CRISPR technology in gene therapy and cancer research, particularly in the context of pancreatic cancer, and lays the foundation for future studies.
胰腺癌的预后较差,死亡率极高,其侵袭性使其被归类为高度恶性疾病。对于有效的治疗策略而言,开发精密且可控的DNA操作方法至关重要。CRISPR/Cas最初是原核免疫系统的一部分,现已成为一种关键的基因组编辑工具,在胰腺癌研究和治疗中具有广阔的应用前景。与早期技术相比,这种基因编辑方法以操作简单、进展迅速和精度更高而闻名。其适应性允许为治疗目的进行精确的基因编辑,包括癌基因沉默和致病突变的校正。此外,CRISPR驱动的基因编辑促进了胰腺癌模型的开发,这些模型是药物发现和个性化治疗策略的宝贵平台,能更深入地洞察胰腺肿瘤的基因格局。本文概述了CRISPR技术在基因治疗和癌症研究中的当前应用,特别是在胰腺癌背景下的应用,并为未来的研究奠定了基础。