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- W2023269839 abstract "Osteosarcoma remains a deadly malignancy afflicting adolescents and young adults. The lack of a precursor and the panoply of genetic aberrations present in identified osteosarcomas makes study of its initiation difficult. A number of candidate hypotheses have been tested in the mouse, a species with a higher background incidence of osteosarcoma. Chemical carcinogens, external beam radiation, and bone-seeking heavy metal radioisotopes have all proven to be osteosarcomagenic in wild-type mice. A number of oncogenes, introduced via integrating viruses or aberrantly activated from heritable genetic loci, participate in and can individually drive osteosarcomagenesis. Germline and conditional gene ablations in the form of some but not all aneuploidy-inducing genes, conventional tumor suppressors, and factors that function normally in mesenchymal differentiation have also proven osteosarcomagenic, especially in combinations that silence the Rb1 and p53 pathways. This paper reviews the rich history of mouse models of osteosarcomagenesis, what they have taught us about the human disease, and what future mouse experiments yet promise to teach." @default.
- W2023269839 created "2016-06-24" @default.
- W2023269839 creator A5046271994 @default.
- W2023269839 date "2011-01-01" @default.
- W2023269839 modified "2023-10-16" @default.
- W2023269839 title "Osteosarcomagenesis: Modeling Cancer Initiation in the Mouse" @default.
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- W2023269839 doi "https://doi.org/10.1155/2011/694136" @default.
- W2023269839 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3043296" @default.
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