Patient-Derived Organoids: A Game-Changer in Personalized Cancer Medicine.

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING Stem Cell Reviews and Reports Pub Date : 2024-10-21 DOI:10.1007/s12015-024-10805-4
Mohammad Hadi Abbasian, Navid Sobhani, Mahsa Mollapour Sisakht, Alberto D'Angelo, Marianna Sirico, Raheleh Roudi
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Abstract

Research on cancer therapies has benefited from predictive tools capable of simulating treatment response and other disease characteristics in a personalized manner, in particular three-dimensional cell culture models. Such models include tumor-derived spheroids, multicellular spheroids including organotypic multicellular spheroids, and tumor-derived organoids. Additionally, organoids can be grown from various cancer cell types, such as pluripotent stem cells and induced pluripotent stem cells, progenitor cells, and adult stem cells. Although patient-derived xenografts and genetically engineered mouse models replicate human disease in vivo, organoids are less expensive, less labor intensive, and less time-consuming, all-important aspects in high-throughput settings. Like in vivo models, organoids mimic the three-dimensional structure, cellular heterogeneity, and functions of primary tissues, with the advantage of representing the normal oxygen conditions of patient organs. In this review, we summarize the use of organoids in disease modeling, drug discovery, toxicity testing, and precision oncology. We also summarize the current clinical trials using organoids.

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源自患者的器官组织:改变个性化癌症医学的游戏规则。
癌症疗法研究得益于能够以个性化方式模拟治疗反应和其他疾病特征的预测工具,特别是三维细胞培养模型。此类模型包括肿瘤衍生球形体、多细胞球形体(包括器官型多细胞球形体)和肿瘤衍生器官体。此外,器官组织可由各种癌症细胞类型培育而成,如多能干细胞和诱导多能干细胞、祖细胞和成体干细胞。虽然患者来源的异种移植物和基因工程小鼠模型可在体内复制人类疾病,但在高通量环境中,器官组织成本更低、劳动强度更小、耗时更少,这些都是非常重要的方面。与体内模型一样,器官组织也能模拟原生组织的三维结构、细胞异质性和功能,其优势在于能代表患者器官的正常供氧条件。在这篇综述中,我们总结了器官组织在疾病建模、药物发现、毒性测试和精准肿瘤学中的应用。我们还总结了目前使用有机体进行的临床试验。
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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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