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An organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.用于儿童肾癌的类器官生物库,可捕获疾病和组织异质性。
Nat Commun. 2020 Mar 11;11(1):1310. doi: 10.1038/s41467-020-15155-6.
2
A Patient-Derived Glioblastoma Organoid Model and Biobank Recapitulates Inter- and Intra-tumoral Heterogeneity.患者来源的脑胶质瘤类器官模型和生物库再现了肿瘤内和肿瘤间的异质性。
Cell. 2020 Jan 9;180(1):188-204.e22. doi: 10.1016/j.cell.2019.11.036. Epub 2019 Dec 26.
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Bone sarcoma patient-derived xenografts are faithful and stable preclinical models for molecular and therapeutic investigations.骨肉瘤患者来源异种移植是用于分子和治疗研究的忠实且稳定的临床前模型。
Sci Rep. 2019 Aug 21;9(1):12174. doi: 10.1038/s41598-019-48634-y.
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Cancer modeling meets human organoid technology.癌症建模与人类类器官技术相遇。
Science. 2019 Jun 7;364(6444):952-955. doi: 10.1126/science.aaw6985.
5
Regorafenib regressed a doxorubicin-resistant Ewing's sarcoma in a patient-derived orthotopic xenograft (PDOX) nude mouse model.regorafenib 使 doxorubicin 耐药的尤文肉瘤在患者来源的原位异种移植(PDOX)裸鼠模型中消退。
Cancer Chemother Pharmacol. 2019 May;83(5):809-815. doi: 10.1007/s00280-019-03782-w. Epub 2019 Feb 13.
6
Combining Tumor-Selective Bacterial Therapy with Salmonella typhimurium A1-R and Cancer Metabolism Targeting with Oral Recombinant Methioninase Regressed an Ewing's Sarcoma in a Patient-Derived Orthotopic Xenograft Model.肿瘤选择性细菌治疗联合鼠伤寒沙门氏菌 A1-R 与口服重组蛋氨酸酶靶向治疗在患者来源的原位异种移植模型中消退尤文肉瘤。
Chemotherapy. 2018;63(5):278-283. doi: 10.1159/000495574. Epub 2019 Jan 23.
7
Genomic evolution of cancer models: perils and opportunities.癌症模型的基因组进化:风险与机遇。
Nat Rev Cancer. 2019 Feb;19(2):97-109. doi: 10.1038/s41568-018-0095-3.
8
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Cell. 2018 Dec 13;175(7):1972-1988.e16. doi: 10.1016/j.cell.2018.11.021.
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尤因肉瘤患者来源模型的现状与展望

Current Status and Perspectives of Patient-Derived Models for Ewing's Sarcoma.

作者信息

Kondo Tadashi

机构信息

Division of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.

出版信息

Cancers (Basel). 2020 Sep 4;12(9):2520. doi: 10.3390/cancers12092520.

DOI:10.3390/cancers12092520
PMID:32899796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7563399/
Abstract

Patient-derived cancer models, including cell lines, organoids, and xenografts, are indispensable tools in cancer research. These models, which recapitulate molecular features of original tumors, allow studies on the biological significance of cancer-associated genes, antitumor effects of novel agents, and molecular mechanisms underlying clinical behaviors of tumors. Moreover, the predictive utility of patient-derived cancer models is expected to facilitate drug development and precision medicine. Ewing's sarcoma is a highly aggressive mesenchymal tumor with a high metastasis rate. Previous studies demonstrated the utility of cell lines and xenografts in Ewing's sarcoma research and clinical studies. However, the number of Ewing's sarcoma models available from public biobanks is limited; this creates an obstacle for research on Ewing's sarcoma. Novel Ewing's sarcoma models are needed to establish their utility, further our understanding of the molecular mechanisms, and help develop effective therapeutic strategies. In this review, the current status of patient-derived cancer models is overviewed, and future prospects of model development are discussed from the perspective of Ewing's sarcoma research. It should be of interest to researchers and clinicians who work on patient-derived cancer models.

摘要

患者来源的癌症模型,包括细胞系、类器官和异种移植,是癌症研究中不可或缺的工具。这些模型概括了原始肿瘤的分子特征,可用于研究癌症相关基因的生物学意义、新型药物的抗肿瘤作用以及肿瘤临床行为的分子机制。此外,患者来源的癌症模型的预测效用有望促进药物开发和精准医学。尤因肉瘤是一种侵袭性很强的间充质肿瘤,转移率很高。先前的研究证明了细胞系和异种移植在尤因肉瘤研究和临床研究中的效用。然而,公共生物样本库中可用的尤因肉瘤模型数量有限;这为尤因肉瘤的研究造成了障碍。需要新型尤因肉瘤模型来确立其效用、加深我们对分子机制的理解并帮助制定有效的治疗策略。在这篇综述中,概述了患者来源的癌症模型的现状,并从尤因肉瘤研究的角度讨论了模型开发的未来前景。这应该会引起从事患者来源的癌症模型研究的研究人员和临床医生的兴趣。