Abstract
Solid tumors are thought to develop and progress by a multi-step process, involving numerous genetic events during tumor evolution (1). Even in cases of familial inheritance, when an individual may already be predisposed to tumorigenesis by carrying a mutation in one allele of a tumor suppressor gene (retinoblastoma, p53, BRCA1, etc.), it is likely that several additional genetic events are required during the progression of a tumor clone from normal epithelium through premalignant, invasive, and metastatic stages. Characterization of the mechanisms underlying tumor progression, and of the genetic events specific to individual tumor types, will lead to improved clinical management and possibly to new therapeutic approaches.
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Waldman, F.M., Sauter, G., Isola, J., Kallioniemi, O., Kallioniemi, A. (1996). Molecular Cytogenetics of Solid Tumor Progression. In: Li, J.J., Li, S.A., Gustafsson, JÃ…., Nandi, S., Sekely, L.I. (eds) Hormonal Carcinogenesis II. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-2332-0_7
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DOI: https://doi.org/10.1007/978-1-4612-2332-0_7
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