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• W2979973632 abstract "Abstract Rapidly accumulating data from large‐scale cancer genomics studies have been generating important information about genes and their somatic alterations underlying cell transformation, cancer onset and tumor progression. However, these events are usually defined by using computational techniques, whereas the understanding of their actual functional roles and impact typically warrants validation by experimental means. Critical information has been obtained from targeted genetic perturbation (gene knockout) studies conducted in animals, yet these investigations are cost‐prohibitive and time‐consuming. In addition, the 3R principles (replacement, reduction, refinement) have been set in place to reduce animal use burden and are increasingly observed in many areas of biomedical research. Consequently, the focus has shifted to new designs of innovative cell‐based experimental models of cell immortalization and transformation in which the critical cancer driver events can be introduced by mutagenic insult and studied functionally, at the level of critical phenotypic readouts. From these efforts, primary cell‐based selective barrier‐bypass models of cell immortalization have emerged as an attractive system that allows studies of the functional relevance of acquired mutations as well as their role as candidate cancer driver events. In this review, we provide an overview of various experimental systems linking carcinogen exposure‐driven cell transformation with the study of cancer driver events. We further describe the advantages and disadvantages of the currently available cell‐based models while outlining future directions for in vitro modeling and functional testing of cancer driver events." @default.
• W2979973632 created "2019-10-18" @default.
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• W2979973632 date "2019-10-31" @default.
• W2979973632 modified "2023-10-18" @default.
• W2979973632 title "Experimental identification of cancer driver alterations in the era of pan‐cancer genomics" @default.
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• W2979973632 doi "https://doi.org/10.1111/cas.14210" @default.
• W2979973632 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6890429" @default.
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