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Titlebook: Cytotoxic Drug Resistance Mechanisms; Robert Brown,Uta B?ger-Brown Book 1999 Humana Press 1999

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書目名稱Cytotoxic Drug Resistance Mechanisms
編輯Robert Brown,Uta B?ger-Brown
視頻videohttp://file.papertrans.cn/243/242691/242691.mp4
叢書名稱Methods in Molecular Medicine
圖書封面Titlebook: Cytotoxic Drug Resistance Mechanisms;  Robert Brown,Uta B?ger-Brown Book 1999 Humana Press 1999
描述There is now a range of cytotoxic drugs that have considerable clinical usefulness in producing responses in tumors and even, in a small proportion of cases, cure. However, the acquisition of drug resistance is a major clinical problem and is perhaps the main limiting factor in successful treatment of cancer. Thus, a tumor initially sensitive to chemotherapy will, in the majority of cases, eventually recur as a resistant tumor, which will then progress. Much of our understanding of drug resistance mechanisms comes from the study of tumor cell lines grown in tissue culture. We now understand many of the - lecular mechanisms that can lead to a cell acquiring resistance to antic- cer drugs; however, we still do not know which mechanism(s) are those most relevant to the problem of clinical drug resistance. Indeed, given that many of the cytotoxic anticancer drugs were discovered by random screening, it is - clear what features give a clinically useful anticancer drug a sufficient the- peutic index to be of value. The aim of Cytotoxic Drug Resistance Mechanisms is to provide pro- cols that are appropriate for examining the mechanisms of cellular resistance to anticancer cytotoxics in hu
出版日期Book 1999
版次1
doihttps://doi.org/10.1385/1592596878
isbn_softcover978-1-61737-093-9
isbn_ebook978-1-59259-687-4Series ISSN 1543-1894 Series E-ISSN 1940-6037
issn_series 1543-1894
copyrightHumana Press 1999
The information of publication is updating

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Analysis of Apoptosis in Tissue Sections,has been well-reviewed (.–.). In addition there is increasing recognition that many of the effects of chemo- and radiotherapeutic agents are mediated by apoptosis (.–.). The seminal work of Kerr, Wyllie, and Currie (.), building upon the earlier observations of Glucksmann (.) and Saunders (.), shoul
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Measurement of P-glycoprotein Function,his phenomenon is called multidrug resistance (MDR). The finding that this gene was expressed in many types of human cancers has stimulated many studies into the relevance of this protein for clinical chemotherapy resistance (.). Pgp is a protein that causes a net transport of substrate drug molecul
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Microtiter Plate Technique for the Measurement of Glutathione in Fresh and Cryopreserved Lymphoblas been implicated in the control of cell cycling (.,.) and apoptosis (.,.). It can exist in an oxidized (disulfide, [GSSG]) and a reduced (sulphydryl, [GSH]) form. In general, GSSG comprises less than 1% of the total intracellular glutathione. In circumstances of oxidative stress, GSH dimerizes to fo
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Measurement of Reduced Glutathione Using High-Pressure Liquid Chromatography,lysis can lead to rapid oxidation to the oxidized form, GSSG, and degradation by γ-glutamyl transpeptidase. In order to obtain a true measurement of the amount of reduced glutathione (GSH) in living cells we have utilized the method of Cotgreave and Moldeus (.) in which GSH is derivatized using mono
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