Mukhare Rushikesh, Gandhi Khushboo A, Kadam Anushree, Raja Aishwarya, Singh Ankita, Madhav Mrudula, Chaubal Rohan, Pandey Shwetali, Gupta Sudeep
Clinical Genomics and Hypoxia Lab (Clinician Scientist Laboratory), Advanced Centre for Treatment, Research, and Education in Cancer, Tata Memorial Centre, Navi Mumbai, Maharashtra, India.
Training School Complex, Homi Bhabha National Institute, Mumbai, Maharashtra, India.
Biol Cell. 2025 Apr;117(4):e70006. doi: 10.1111/boc.70006.
Organoids represent a significant advancement in disease modeling, demonstrated by their capacity to mimic the physiological/pathological structure and functional characteristics of the native tissue. Recently CRISPR/Cas9 technology has emerged as a powerful tool in combination with organoids for the development of novel therapies in preclinical settings. This review explores the current literature on applications of pooled CRISPR screening in organoids and the emerging role of these models in understanding cancer. We highlight the evolution of genome-wide CRISPR gRNA library screens in organoids, noting their increasing adoption in the field over the past decade. Noteworthy studies utilizing these screens to investigate oncogenic vulnerabilities and developmental pathways in various organoid systems are discussed. Despite the promise organoids hold, challenges such as standardization, reproducibility, and the complexity of data interpretation remain. The review also addresses the ideas of assessing tumor organoids (tumoroids) against established cancer hallmarks and the potential of studying intercellular cooperation within these models. Ultimately, we propose that organoids, particularly when personalized for patient-specific applications, could revolutionize drug screening and therapeutic approaches, minimizing the reliance on traditional animal models and enhancing the precision of clinical interventions.
类器官代表了疾病建模领域的一项重大进展,其能够模拟天然组织的生理/病理结构及功能特征,已证明了这一点。最近,CRISPR/Cas9技术已成为一种强大的工具,可与类器官相结合,用于临床前环境中新型疗法的开发。本综述探讨了关于在类器官中进行CRISPR筛选池应用的当前文献,以及这些模型在理解癌症方面的新作用。我们强调了类器官中全基因组CRISPR gRNA文库筛选的发展历程,注意到在过去十年中它们在该领域的应用日益增多。讨论了利用这些筛选来研究各种类器官系统中致癌易感性和发育途径的重要研究。尽管类器官前景广阔,但仍存在标准化、可重复性和数据解释复杂性等挑战。本综述还探讨了根据既定癌症特征评估肿瘤类器官(肿瘤样体)的思路,以及在这些模型中研究细胞间合作的潜力。最终,我们提出类器官,特别是针对患者特异性应用进行个性化定制时,可能会彻底改变药物筛选和治疗方法,减少对传统动物模型的依赖,并提高临床干预的精准度。