Kitos Biotech Srls, Tramariglio, Alghero (SS), Italy.
Department of Biomedical Sciences, University of Sassari, Sassari, Italy.
J Cell Physiol. 2018 May;233(5):4106-4115. doi: 10.1002/jcp.26208. Epub 2017 Dec 4.
Cell proliferation assays are performed by four decades to test the anti-proliferative activity of natural products and synthetic compounds in cell cultures. In cancer research, they are widely employed to evaluate drug efficacy in in vitro tumor models, such as established cell lines, primary cultures, and recently developed three-dimensional tumor organoids. In this manuscript, we demonstrated that current employed parameters used by researchers to quantify in vitro growth inhibition, IC and GI , lead to a misinterpretation of results based on the exponential, and not linear, proliferation of the cells in culture. Therefore, we introduce a new parameter for the analysis of growth inhibition in cell proliferation assays, termed relative population doubling capacity, that can be employed to properly quantify the anti-proliferative activity of tested compounds and to compare drug efficacy between distinct cell models.
细胞增殖检测方法已经使用了几十年,用于测试天然产物和合成化合物在细胞培养物中的抗增殖活性。在癌症研究中,它们被广泛用于评估体外肿瘤模型(如已建立的细胞系、原代培养物和最近开发的三维肿瘤类器官)中的药物疗效。在本文中,我们证明了当前研究人员用于量化体外生长抑制的参数,IC 和 GI ,基于细胞在培养中的指数而非线性增殖,导致对结果的误解。因此,我们引入了一个新的参数,用于细胞增殖检测中的生长抑制分析,称为相对群体倍增能力,可用于正确量化测试化合物的抗增殖活性,并比较不同细胞模型之间的药物疗效。