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Titlebook: Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches; Proceedings of the 1 Frederick A. Valeriote,Laurence H.

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期刊全称Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches
期刊简称Proceedings of the 1
影响因子2023Frederick A. Valeriote,Laurence H. Baker
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学科分类Developments in Oncology
图书封面Titlebook: Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches; Proceedings of the 1 Frederick A. Valeriote,Laurence H.
影响因子Biochemical Modulation at the present time defines an area of study in which the intracellular metabolism of a given anti­ cancer agent is modulated (usually by a noncytotoxic agent or a cytotoxic agent at sufficiently low dosage to make it non­ cytotoxic) in order to either increase the effectiveness of the particular agent against tumor cells or decrease its cytotox­ icity against normal cells. The major focus of modulation has been the agents 5-fluorouracil (FUra), arabinofuranosylcytosine (ara-C), methotrexate (MTX) and a few alkylating agents. The major thrust of the studies has been to increase the flow of the anticancer agent along the pathway responsible for the formation of the cytotoxic species: for example, FUra to FUTP or ara-C to ara-CTP. While in most cases the application of research re­ sults to clinical trials does not require the subsequent exper­ tise of the laboratory researchers, application of biochemical modulatory schemes to clinical protocols necessitate a dramatic break with the past procedures. As shown in the laboratory­ clinical loop below, close collaboration between the laboratory and clinical investigator is essential. While the laboratory REDEFINE T
Pindex Conference proceedings 1986
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https://doi.org/10.1007/978-1-4613-2331-0Purine; Pyrimidine; cell; clinical trial; metabolism; tumor
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978-1-4612-9432-0Martinus Nijhoff Publishing, Boston 1986
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https://doi.org/10.1007/978-3-030-79489-7tivity against a given normal or tumor cell population are employed to . of an .anticancer agent. The modulation can be either to increase the cytotoxicity of the anticancer agent against clonogenic tumor cells or to decrease the cytotoxicity of the anticancer agent against cells of the dose-limitin
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Journeys in Argentine and Brazilian Cinemaism and the consequence of these perturbations on a second drug is the foundation of the principles of biochemical modulation. Our research laboratories have been investigating the modulating effects of drugs that either increase or decrease intracellular levels of 5-phosphoribosyl-1-pyrophosphate (
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