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利用软琼脂集落形成试验鉴定乳腺癌细胞致瘤性抑制剂

Utilization of the Soft Agar Colony Formation Assay to Identify Inhibitors of Tumorigenicity in Breast Cancer Cells.

作者信息

Horibata Sachi, Vo Tommy V, Subramanian Venkataraman, Thompson Paul R, Coonrod Scott A

机构信息

Department of Baker Institute for Animal Health, Cornell University.

Department of Molecular Biology and Genetics, Cornell University.

出版信息

J Vis Exp. 2015 May 20(99):e52727. doi: 10.3791/52727.

Abstract

Given the inherent difficulties in investigating the mechanisms of tumor progression in vivo, cell-based assays such as the soft agar colony formation assay (hereafter called soft agar assay), which measures the ability of cells to proliferate in semi-solid matrices, remain a hallmark of cancer research. A key advantage of this technique over conventional 2D monolayer or 3D spheroid cell culture assays is the close mimicry of the 3D cellular environment to that seen in vivo. Importantly, the soft agar assay also provides an ideal tool to rigorously test the effects of novel compounds or treatment conditions on cell proliferation and migration. Additionally, this assay enables the quantitative assessment of cell transformation potential within the context of genetic perturbations. We recently identified peptidylarginine deiminase 2 (PADI2) as a potential breast cancer biomarker and therapeutic target. Here we highlight the utility of the soft agar assay for preclinical anti-cancer studies by testing the effects of the PADI inhibitor, BB-Cl-amidine (BB-CLA), on the tumorigenicity of human ductal carcinoma in situ (MCF10DCIS) cells.

摘要

鉴于在体内研究肿瘤进展机制存在固有的困难,基于细胞的检测方法,如软琼脂集落形成检测法(以下简称软琼脂检测法),该方法可测量细胞在半固体基质中增殖的能力,仍然是癌症研究的一个标志。与传统的二维单层或三维球体细胞培养检测法相比,该技术的一个关键优势在于其能紧密模拟体内所见的三维细胞环境。重要的是,软琼脂检测法还提供了一个理想的工具,用于严格测试新型化合物或治疗条件对细胞增殖和迁移的影响。此外,该检测法能够在基因扰动的背景下对细胞转化潜能进行定量评估。我们最近将肽基精氨酸脱亚氨酶2(PADI2)鉴定为一种潜在的乳腺癌生物标志物和治疗靶点。在此,我们通过测试PADI抑制剂BB-氯脒(BB-CLA)对人原位导管癌(MCF10DCIS)细胞致瘤性的影响,突出软琼脂检测法在临床前抗癌研究中的实用性。

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