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Comprehensive Drug Testing of Patient-derived Conditionally Reprogrammed Cells from Castration-resistant Prostate Cancer.对去势抵抗性前列腺癌患者来源的条件重编程细胞进行全面药物测试。
Eur Urol. 2017 Mar;71(3):319-327. doi: 10.1016/j.eururo.2016.04.019. Epub 2016 May 6.
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Analogs of the novel phytohormone, strigolactone, trigger apoptosis and synergize with PARP inhibitors by inducing DNA damage and inhibiting DNA repair.新型植物激素独脚金内酯的类似物通过诱导DNA损伤和抑制DNA修复来触发细胞凋亡,并与聚(ADP-核糖)聚合酶(PARP)抑制剂协同作用。
Oncotarget. 2016 Mar 22;7(12):13984-4001. doi: 10.18632/oncotarget.7414.
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Organoid culture systems for prostate epithelial and cancer tissue.用于前列腺上皮和癌组织的类器官培养系统。
Nat Protoc. 2016 Feb;11(2):347-58. doi: 10.1038/nprot.2016.006. Epub 2016 Jan 21.
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SpOT the Correct Tissue Every Time in Multi-tissue Blocks.每次在多组织块中精准定位正确组织。
J Vis Exp. 2015 May 31(99):e52868. doi: 10.3791/52868.
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The induction of the p53 tumor suppressor protein bridges the apoptotic and autophagic signaling pathways to regulate cell death in prostate cancer cells.p53肿瘤抑制蛋白的诱导作用连接了凋亡和自噬信号通路,以调节前列腺癌细胞中的细胞死亡。
Oncotarget. 2014 Nov 15;5(21):10678-91. doi: 10.18632/oncotarget.2528.
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Organoid cultures derived from patients with advanced prostate cancer.源自晚期前列腺癌患者的类器官培养物。
Cell. 2014 Sep 25;159(1):176-187. doi: 10.1016/j.cell.2014.08.016. Epub 2014 Sep 4.
7
Patient-derived xenograft models: an emerging platform for translational cancer research.患者来源的异种移植模型:一个用于转化癌症研究的新兴平台。
Cancer Discov. 2014 Sep;4(9):998-1013. doi: 10.1158/2159-8290.CD-14-0001. Epub 2014 Jul 15.
8
Strigolactone analogues induce apoptosis through activation of p38 and the stress response pathway in cancer cell lines and in conditionally reprogrammed primary prostate cancer cells.独脚金内酯类似物通过激活p38和癌细胞系及条件重编程原代前列腺癌细胞中的应激反应途径诱导细胞凋亡。
Oncotarget. 2014 Mar 30;5(6):1683-98. doi: 10.18632/oncotarget.1849.
9
Radiation induces diffusible feeder cell factor(s) that cooperate with ROCK inhibitor to conditionally reprogram and immortalize epithelial cells.辐射诱导扩散性饲养细胞因子与 ROCK 抑制剂协同作用,条件性重编程并永生化上皮细胞。
Am J Pathol. 2013 Dec;183(6):1862-1870. doi: 10.1016/j.ajpath.2013.08.009. Epub 2013 Oct 3.
10
Use of reprogrammed cells to identify therapy for respiratory papillomatosis.利用重编程细胞鉴定呼吸道乳头瘤病的治疗方法。
N Engl J Med. 2012 Sep 27;367(13):1220-7. doi: 10.1056/NEJMoa1203055.

一种基于快速滤器插入物的用于原代前列腺细胞分化的3D培养系统。

A Rapid Filter Insert-based 3D Culture System for Primary Prostate Cell Differentiation.

作者信息

Tricoli Lucas, Berry Deborah L, Albanese Chris

机构信息

Department of Oncology, Lombardi Comprehensive Cancer Center.

Department of Oncology, Georgetown University Medical Center.

出版信息

J Vis Exp. 2017 Feb 13(120):55279. doi: 10.3791/55279.

DOI:10.3791/55279
PMID:28287583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5408911/
Abstract

Conditionally reprogrammed cells (CRCs) provide a sustainable method for primary cell culture and the ability to develop extensive "living biobanks" of patient derived cell lines. For many types of epithelial cells, various three dimensional (3D) culture approaches have been described that support an improved differentiated state. While CRCs retain their lineage commitment to the tissue from which they are isolated, they fail to express many of the differentiation markers associated with the tissue of origin when grown under normal two dimensional (2D) culture conditions. To enhance the application of patient-derived CRCs for prostate cancer research, a 3D culture format has been defined that enables a rapid (2 weeks total) luminal cell differentiation in both normal and tumor-derived prostate epithelial cells. Herein, a filter insert-based format is described for the culturing and differentiation of both normal and malignant prostate CRCs. A detailed description of the procedures required for cell collection and processing for immunohistochemical and immunofluorescent staining are provided. Collectively the 3D culture format described, combined with the primary CRC lines, provides an important medium- to high- throughput model system for biospecimen-based prostate research.

摘要

条件重编程细胞(CRCs)为原代细胞培养提供了一种可持续的方法,并具备建立大量患者来源细胞系“活生物样本库”的能力。对于多种类型的上皮细胞,已有多种三维(3D)培养方法被描述,这些方法能支持细胞达到更好的分化状态。虽然CRCs保留了它们对所分离组织的谱系定向,但在正常二维(2D)培养条件下生长时,它们无法表达许多与起源组织相关的分化标志物。为了增强患者来源的CRCs在前列腺癌研究中的应用,已定义了一种3D培养形式,该形式能使正常和肿瘤来源的前列腺上皮细胞快速(总共2周)向管腔细胞分化。本文描述了一种基于滤膜插入物的形式,用于正常和恶性前列腺CRCs的培养和分化。还提供了细胞收集以及用于免疫组织化学和免疫荧光染色的处理所需程序的详细说明。总体而言,所描述的3D培养形式与原代CRCs细胞系相结合,为基于生物样本的前列腺研究提供了一个重要的中高通量模型系统。