Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, Finland.
Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, Finland; Department of Pathology, University of Turku, Turku, Finland; Turku Doctoral Program of Biomedical Sciences, University of Turku and Åbo Akademi University, Turku, Finland.
PLoS One. 2014 Mar 19;9(3):e92444. doi: 10.1371/journal.pone.0092444. eCollection 2014.
The clonogenic or colony formation assay is a widely used method to study the number and size of cancer cell colonies that remain after irradiation or cytotoxic agent administration and serves as a measure for the anti-proliferative effect of these treatments. Alternatively, this assay is used to quantitate the transforming potential of cancer associated genes and chemical agents. Therefore, there is a need for a simplified and standardized analysis of colony formation assays for both routine laboratory use and for parallelized automated analysis. Here we describe the freely available ImageJ-plugin "ColonyArea", which is optimized for rapid and quantitative analysis of focus formation assays conducted in 6- to 24-well dishes. ColonyArea processes image data of multi-well dishes, by separating, concentrically cropping and background correcting well images individually, before colony formation is quantitated. Instead of counting the number of colonies, ColonyArea determines the percentage of area covered by crystal violet stained cell colonies, also taking the intensity of the staining and therefore cell density into account. We demonstrate that these parameters alone or in combination allow for robust quantification of IC50 values of the cytotoxic effect of two staurosporines, UCN-01 and staurosporine (STS) on human glioblastoma cells (T98G). The relation between the potencies of the two compounds compared very well with that obtained from an absorbance based method to quantify colony growth and to published data. The ColonyArea ImageJ plugin provides a simple and efficient analysis routine to quantitate assay data of one of the most commonly used cellular assays. The bundle is freely available for download as supporting information. We expect that ColonyArea will be of broad utility for cancer biologists, as well as clinical radiation scientists.
集落形成分析是一种广泛应用的方法,用于研究在照射或细胞毒性剂处理后仍存在的癌细胞集落的数量和大小,可作为这些处理的抗增殖作用的度量。或者,该测定法用于定量癌症相关基因和化学试剂的转化潜能。因此,需要对集落形成测定法进行简化和标准化分析,以便于常规实验室使用和并行自动化分析。在这里,我们描述了免费提供的 ImageJ 插件“ColonyArea”,该插件针对在 6 孔至 24 孔板中进行的焦点形成测定进行了快速和定量分析进行了优化。ColonyArea 对微孔板的图像数据进行处理,通过单独分离、同心裁剪和背景校正各个孔图像,然后对集落形成进行定量分析。ColonyArea 不计数集落的数量,而是确定结晶紫染色细胞集落覆盖的面积百分比,同时还考虑染色的强度和细胞密度。我们证明,这些参数单独或组合使用可以可靠地量化两种司他丁类药物 UCN-01 和司他丁(STS)对人神经胶质瘤细胞(T98G)的细胞毒性作用的 IC50 值。两种化合物的效力之间的关系与从基于吸光度的方法获得的关系非常吻合,该方法用于定量集落生长并与已发表的数据进行比较。ColonyArea ImageJ 插件提供了一种简单而有效的分析程序,用于定量最常用的细胞测定之一的测定数据。捆绑包可作为支持信息免费下载。我们希望 ColonyArea 将对癌症生物学家以及临床放射科学家具有广泛的实用性。