Abstract
The p73 gene has a complex regulation, which leads to the expression of different isoforms, often with opposite biological effects. We have generated in the human colocarcinoma cell line HCT116, expressing a wild-type p53, an inducible DNp73α expressing system. Two clones (HCT116/DN3 and HCT116/DN14), upon doxycycline addition, show a strong expression of DNp73α. In vitro the two DNp73α overexpressing clones grow at similar rate of the control transfected clone (HCT116/8a) and similarly respond to DNA damage. When injected in mice, HCT116/DN3, HCT116/DN14, and HCT116/8a cells grew similarly in the absence or presence of tetracycline. In HCT116/DN3 and HCT116/DN14 tumors, tetracycline induced a strong expression of DNp73α both as mRNA and protein. These results indicate that in this system the overexpression of the DNp73α does not induce a more aggressive phenotype and does not seem to be associated with a reduced response of the cells to treatment with anticancer agents. © 2005 Nature Publishing Group. All rights reserved.
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Marabese, M., Marchini, S., Sabatino, M. A., Polato, F., Vikhanskaya, F., Marrazzo, E., … Broggini, M. (2005). Effects of inducible overexpression of DNp73α on cancer cell growth and response to treatment in vitro and in vivo. Cell Death and Differentiation, 12(7), 805–814. https://doi.org/10.1038/sj.cdd.4401622
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