Abstract
The last 15 years have seen a virtual explosion in knowledge of cancer at the molecular level. Major efforts in the area of molecular genetics were stimulated by a study of viral oncogenes (1) and have centered around the activation of proto-oncogenes, which code for proteins that are involved in the signal transduction events that modulate normal cellular growth and differentiation. More that one hundred normal cellular proto-oncogenes are now known (2). Mechanisms of activation of proto-oncogenes to cellular oncogenes include point mutation, deletion, insertion, amplification, activation by internal rearrangement, chromosomal translocation, and promoter insertion (3). Cancer would appear to have many causes, but a common element is DNA damage resulting in aberrant gene expression which is a multi-step process (4). Chromosomal analyses of tumor cells have revealed many abnormal karyotypes with metastases as the most aberrant. Most cancers exhibit some cytogenetic defect (5).
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Robins, R.K., Finch, R.A., Avery, T.L. (1994). Nucleoside and Nucleotide Modulation of Oncogenic Expression: A New Approach to Cancer Chemotherapy. In: Valeriote, F.A., Corbett, T.H., Baker, L.H. (eds) Anticancer Drug Discovery and Development: Natural Products and New Molecular Models. Developments in Oncology, vol 74. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-2610-0_9
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