Janitri Venkatachalababu, ArulJothi Kandasamy Nagarajan, Ravi Mythili Vijay Murali, Singh Sachin Kumar, Prasher Parteek, Gupta Gaurav, Dua Kamal, Hanumanthappa Rakshith, Karthikeyan Karthikeyan, Anand Krishnan
Department of Biomedical Engineering Rochester Institute of Technology Rochester New York USA.
Department of Genetic Engineering, College of Engineering and Technology SRM Institute of Science and Technology Chengalpattu Tamil Nadu India.
MedComm (2020). 2024 Sep 25;5(10):e745. doi: 10.1002/mco2.745. eCollection 2024 Oct.
Patient-derived xenografts (PDX) involve transplanting patient cells or tissues into immunodeficient mice, offering superior disease models compared with cell line xenografts and genetically engineered mice. In contrast to traditional cell-line xenografts and genetically engineered mice, PDX models harbor the molecular and biologic features from the original patient tumor and are generationally stable. This high fidelity makes PDX models particularly suitable for preclinical and coclinical drug testing, therefore better predicting therapeutic efficacy. Although PDX models are becoming more useful, the several factors influencing their reliability and predictive power are not well understood. Several existing studies have looked into the possibility that PDX models could be important in enhancing our knowledge with regard to tumor genetics, biomarker discovery, and personalized medicine; however, a number of problems still need to be addressed, such as the high cost and time-consuming processes involved, together with the variability in tumor take rates. This review addresses these gaps by detailing the methodologies to generate PDX models, their application in cancer research, and their advantages over other models. Further, it elaborates on how artificial intelligence and machine learning were incorporated into PDX studies to fast-track therapeutic evaluation. This review is an overview of the progress that has been done so far in using PDX models for cancer research and shows their potential to be further improved in improving our understanding of oncogenesis.
患者来源的异种移植(PDX)涉及将患者的细胞或组织移植到免疫缺陷小鼠体内,与细胞系异种移植和基因工程小鼠相比,它能提供更优的疾病模型。与传统的细胞系异种移植和基因工程小鼠不同,PDX模型保留了原始患者肿瘤的分子和生物学特征,并且具有代际稳定性。这种高保真度使得PDX模型特别适合临床前和临床联合药物测试,从而能更好地预测治疗效果。尽管PDX模型正变得越来越有用,但影响其可靠性和预测能力的几个因素尚未得到充分理解。现有的一些研究探讨了PDX模型在增强我们对肿瘤遗传学、生物标志物发现和个性化医疗的认识方面可能具有重要意义;然而,仍有一些问题需要解决,例如涉及的高成本和耗时过程,以及肿瘤植入率的变异性。本综述通过详细介绍生成PDX模型的方法、它们在癌症研究中的应用以及它们相对于其他模型的优势,填补了这些空白。此外,它还阐述了如何将人工智能和机器学习纳入PDX研究以加快治疗评估。本综述概述了迄今为止在使用PDX模型进行癌症研究方面所取得的进展,并展示了它们在增进我们对肿瘤发生的理解方面进一步改进的潜力。