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Cancer Res. 2015 Aug 1;75(15):2963-8. doi: 10.1158/0008-5472.CAN-15-0727. Epub 2015 Jul 15.
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A NOTCH1 gene copy number gain is a prognostic indicator of worse survival and a predictive biomarker to a Notch1 targeting antibody in colorectal cancer.NOTCH1基因拷贝数增加是结直肠癌患者生存预后较差的一个指标,也是针对Notch1的靶向抗体的预测生物标志物。
Int J Cancer. 2016 Jan 1;138(1):195-205. doi: 10.1002/ijc.29676. Epub 2015 Jul 22.
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Combined inhibition of MEK and Aurora A kinase in KRAS/PIK3CA double-mutant colorectal cancer models.在KRAS/PIK3CA双突变结直肠癌模型中联合抑制MEK和Aurora A激酶
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Tumours with elevated levels of the Notch and Wnt pathways exhibit efficacy to PF-03084014, a γ-secretase inhibitor, in a preclinical colorectal explant model.在结直肠外植体模型中,Notch 和 Wnt 通路水平升高的肿瘤对 γ-分泌酶抑制剂 PF-03084014 有效。
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Rational combination of a MEK inhibitor, selumetinib, and the Wnt/calcium pathway modulator, cyclosporin A, in preclinical models of colorectal cancer.在结直肠癌的临床前模型中,MEK 抑制剂塞尔美替尼与 Wnt/钙通路调节剂环孢素 A 的合理联合。
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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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用于研究新型抗癌疗法的临床前患者来源肿瘤异种移植模型的建立与维持

Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies.

作者信息

Bagby Stacey, Messersmith Wells A, Pitts Todd M, Capasso Anna, Varella-Garcia Marileila, Klauck Peter J, Kim Jihye, Tan Aik-Choon, Eckhardt S Gail, Tentler John J, Arcaroli John

机构信息

Medicine, University of Colorado Denver Anschutz Medical Campus.

Medicine, University of Colorado Denver Anschutz Medical Campus;

出版信息

J Vis Exp. 2016 Sep 30(115):54393. doi: 10.3791/54393.

DOI:10.3791/54393
PMID:27768028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5092181/
Abstract

Patient derived tumor xenograft (PDTX) models provide a necessary platform in facilitating anti-cancer drug development prior to human trials. Human tumor pieces are injected subcutaneously into athymic nude mice (immunocompromised, T cell deficient) to create a bank of tumors and subsequently are passaged into different generations of mice in order to maintain these tumors from patients. Importantly, cellular heterogeneity of the original tumor is closely emulated in this model, which provides a more clinically relevant model for evaluation of drug efficacy studies (single agent and combination), biomarker analysis, resistant pathways and cancer stem cell biology. Some limitations of the PDTX model include the replacement of the human stroma with mouse stroma after the first generation in mice, inability to investigate treatment effects on metastasis due to the subcutaneous injections of the tumors, and the lack of evaluation of immunotherapies due to the use of immunocompromised mice. However, even with these limitations, the PDTX model provides a powerful preclinical platform in the drug discovery process.

摘要

患者来源的肿瘤异种移植(PDTX)模型为在人体试验之前促进抗癌药物研发提供了一个必要的平台。将人肿瘤组织皮下注射到无胸腺裸鼠(免疫缺陷、T细胞缺陷)体内,以建立肿瘤库,随后将其传代至不同代的小鼠体内,以维持这些源自患者的肿瘤。重要的是,该模型能紧密模拟原始肿瘤的细胞异质性,为评估药物疗效研究(单药和联合用药)、生物标志物分析、耐药途径和癌症干细胞生物学提供了一个更具临床相关性的模型。PDTX模型的一些局限性包括在小鼠体内传至第一代后,人基质被小鼠基质取代;由于肿瘤是皮下注射,无法研究对转移的治疗效果;以及由于使用免疫缺陷小鼠而缺乏对免疫疗法的评估。然而,即使存在这些局限性,PDTX模型在药物发现过程中仍提供了一个强大的临床前平台。