Abstract
BackgroundThe most frequently used method to quantitatively describe the response to ionizing irradiation in terms of clonogenic survival is the linear-quadratic (LQ) model. In the LQ model, the logarithm of the surviving fraction is regressed linearly on the radiation dose by means of a second-degree polynomial. The ratio of the estimated parameters for the linear and quadratic term, respectively, represents the dose at which both terms have the same weight in the abrogation of clonogenic survival. This ratio is known as the α/β ratio. However, there are plausible scenarios in which the α/β ratio fails to sufficiently reflect differences between dose-response curves, for example when curves with similar α/β ratio but different overall steepness are being compared. In such situations, the interpretation of the LQ model is severely limited.MethodsColony formation assays were performed in order to measure the clonogenic survival of nine human pancreatic cancer cell lines and immortalized human pancreatic ductal epithelial cells upon irradiation at 0-10 Gy. The resulting dataset was subjected to LQ regression and non-linear log-logistic regression. Dimensionality reduction of the data was performed by cluster analysis and principal component analysis.ResultsBoth the LQ model and the non-linear log-logistic regression model resulted in accurate approximations of the observed dose-response relationships in the dataset of clonogenic survival. However, in contrast to the LQ model the non-linear regression model allowed the discrimination of curves with different overall steepness but similar α/β ratio and revealed an improved goodness-of-fit. Additionally, the estimated parameters in the non-linear model exhibit a more direct interpretation than the α/β ratio. Dimensionality reduction of clonogenic survival data by means of cluster analysis was shown to be a useful tool for classifying radioresistant and sensitive cell lines. More quantitatively, principal component analysis allowed the extraction of scores of radioresistance, which displayed significant correlations with the estimated parameters of the regression models.ConclusionsUndoubtedly, LQ regression is a robust method for the analysis of clonogenic survival data. Nevertheless, alternative approaches including non-linear regression and multivariate techniques such as cluster analysis and principal component analysis represent versatile tools for the extraction of parameters and/or scores of the cellular response towards ionizing irradiation with a more intuitive biological interpretation. The latter are highly informative for correlation analyses with other types of data, including functional genomics data that are increasingly beinggenerated.
Highlights
The most frequently used method to quantitatively describe the response to ionizing irradiation in terms of clonogenic survival is the linear-quadratic (LQ) model
Clonogenic survival of eight human pancreatic cancer cell lines and immortalized human pancreatic ductal epithelial cells (HPDE) was measured by colony formation assays upon exposure to ionizing irradiation, and the resulting dataset was subjected to different computational analyses in order to obtain measures of radioresistance and/or sensitivity
Based on the assumption that clonogenic cell death upon ionizing irradiation derives from lethal DNA damage, which is predominantly represented by DNA double strand breaks (DSBs), the linear term in this model was attributed to DSBs resulting from single irradiation events, whereas the quadratic term was interpreted as DSBs resulting from two independent irradiation events
Summary
The most frequently used method to quantitatively describe the response to ionizing irradiation in terms of clonogenic survival is the linear-quadratic (LQ) model. There are plausible scenarios in which the α/β ratio fails to sufficiently reflect differences between dose-response curves, for example when curves with similar α/β ratio but different overall steepness are being compared In such situations, the interpretation of the LQ model is severely limited. Clonogenic survival is an important endpoint to measure the cellular response towards ionizing irradiation in vitro It is commonly assessed by 2D or 3D colony formation assays, which are based on the capacity of single cells to grow to colonies consisting of at least 50 cells [1,2,3]. Colony formation assays are frequently utilized to examine and characterize differences in sensitivity towards ionizing irradiation between tumor and normal cells and to assess the impact of additional treatments and/or manipulations on the radiation response. Whereas the abrogation of clonogenic survival is of utmost importance for tumor control and for the prevention of recurrences, preservation of continued proliferation and clonogenic survival are a crucial prerequisite for maintaining integrity and function in normal tissue
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