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本文引用的文献

1
p53 deficiency linked to B cell translocation gene 2 (BTG2) loss enhances metastatic potential by promoting tumor growth in primary and metastatic sites in patient-derived xenograft (PDX) models of triple-negative breast cancer.在三阴性乳腺癌患者来源异种移植(PDX)模型中,与B细胞易位基因2(BTG2)缺失相关的p53缺陷通过促进原发和转移部位的肿瘤生长来增强转移潜能。
Breast Cancer Res. 2016 Jan 27;18(1):13. doi: 10.1186/s13058-016-0673-9.
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Imaging TGFβ Signaling in Mouse Models of Cancer Metastasis.在癌症转移小鼠模型中成像转化生长因子β信号传导
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Single-cell analysis reveals a stem-cell program in human metastatic breast cancer cells.单细胞分析揭示了人类转移性乳腺癌细胞中的干细胞程序。
Nature. 2015 Oct 1;526(7571):131-5. doi: 10.1038/nature15260. Epub 2015 Sep 23.
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Modelling breast cancer requires identification and correction of a critical cell lineage-dependent transduction bias.对乳腺癌进行建模需要识别并纠正一种关键的细胞谱系依赖性转导偏差。
Nat Commun. 2015 Apr 21;6:6927. doi: 10.1038/ncomms7927.
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Lessons learned from the intrinsic subtypes of breast cancer in the quest for precision therapy.从乳腺癌内在亚型中汲取的精准治疗经验。
Br J Surg. 2014 Jul;101(8):925-38. doi: 10.1002/bjs.9562. Epub 2014 May 21.
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Mimicking breast cancer-induced bone metastasis in vivo: current transplantation models and advanced humanized strategies.体内模拟乳腺癌诱导的骨转移:当前的移植模型及先进的人源化策略
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Patient-derived xenografts of triple-negative breast cancer reproduce molecular features of patient tumors and respond to mTOR inhibition.三阴性乳腺癌患者来源异种移植物再现患者肿瘤的分子特征,并对 mTOR 抑制有反应。
Breast Cancer Res. 2014 Apr 7;16(2):R36. doi: 10.1186/bcr3640.
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A renewable tissue resource of phenotypically stable, biologically and ethnically diverse, patient-derived human breast cancer xenograft models.一种可再生的组织资源,具有表型稳定、生物和种族多样化、患者来源的人乳腺癌异种移植模型。
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Patient-derived tumor xenografts: transforming clinical samples into mouse models.患者来源的肿瘤异种移植物:将临床样本转化为小鼠模型。
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Lineage depletion of stromal vascular fractions isolated from human adipose tissue: a novel approach towards cell enrichment technology.从人脂肪组织中分离的基质血管部分的谱系耗竭:一种新型的细胞富集技术方法。
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使用可追踪报告基因标记乳腺癌患者来源的异种移植模型用于肿瘤生长和转移研究

Labeling of Breast Cancer Patient-derived Xenografts with Traceable Reporters for Tumor Growth and Metastasis Studies.

作者信息

Hanna Colton, Kwok Letty, Finlay-Schultz Jessica, Sartorius Carol A, Cittelly Diana M

机构信息

Department of Pathology, School of Medicine, University of Colorado Anschutz Medical Campus.

Department of Pathology, School of Medicine, University of Colorado Anschutz Medical Campus;

出版信息

J Vis Exp. 2016 Nov 30(117):54944. doi: 10.3791/54944.

DOI:10.3791/54944
PMID:27929464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5226329/
Abstract

The use of preclinical models to study tumor biology and response to treatment is central to cancer research. Long-established human cell lines, and many transgenic mouse models, often fail to recapitulate the key aspects of human malignancies. Thus, alternative models that better represent the heterogeneity of patients' tumors and their metastases are being developed. Patient-derived xenograft (PDX) models in which surgically resected tumor samples are engrafted into immunocompromised mice have become an attractive alternative as they can be transplanted through multiple generations,and more efficiently reflect tumor heterogeneity than xenografts derived from human cancer cell lines. A limitation to the use of PDXs is that they are difficult to transfect or transduce to introduce traceable reporters or to manipulate gene expression. The current protocol describes methods to transduce dissociated tumor cells from PDXs with high transduction efficiency, and the use of labeled PDXs for experimental models of breast cancer metastases. The protocol also demonstrates the use of labeled PDXs in experimental metastasis models to study the organ-colonization process of the metastatic cascade. Metastases to different organs can be easily visualized and quantified using bioluminescent imaging in live animals, or GFP expression during dissection and in excised organs. These methods provide a powerful tool to extend the use of multiple types of PDXs to metastasis research.

摘要

利用临床前模型研究肿瘤生物学及对治疗的反应是癌症研究的核心。长期以来使用的人类细胞系以及许多转基因小鼠模型,常常无法重现人类恶性肿瘤的关键特征。因此,正在开发能更好地体现患者肿瘤及其转移灶异质性的替代模型。将手术切除的肿瘤样本植入免疫缺陷小鼠体内构建的患者来源异种移植(PDX)模型,已成为一种颇具吸引力的替代方案,因为它们可以传代移植,并且比源自人类癌细胞系的异种移植更有效地反映肿瘤异质性。使用PDX模型的一个局限在于,难以对其进行转染或转导以引入可追踪的报告基因或操纵基因表达。本实验方案描述了以高效转导效率转导来自PDX的解离肿瘤细胞的方法,以及将标记的PDX用于乳腺癌转移实验模型的方法。该方案还展示了在实验性转移模型中使用标记的PDX来研究转移级联反应中的器官定植过程。利用活体动物的生物发光成像,或在解剖及切除器官过程中观察绿色荧光蛋白(GFP)表达,可轻松可视化并定量不同器官的转移灶。这些方法为将多种类型的PDX模型扩展应用于转移研究提供了有力工具。