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Titlebook: Real-Time Monitoring of Cancer Cell Metabolism for Drug Testing; Hamed Alborzinia Book 2015 Springer Fachmedien Wiesbaden 2015 Biosensor C

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發(fā)表于 2025-3-21 20:10:05 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Real-Time Monitoring of Cancer Cell Metabolism for Drug Testing
編輯Hamed Alborzinia
視頻videohttp://file.papertrans.cn/823/822278/822278.mp4
概述Publication in the field of natural sciences.Includes supplementary material:
圖書封面Titlebook: Real-Time Monitoring of Cancer Cell Metabolism for Drug Testing;  Hamed Alborzinia Book 2015 Springer Fachmedien Wiesbaden 2015 Biosensor C
描述Hamed Alborzinia uses the biosensor chip to monitor the metabolic and morphological changes in cancer cell lines in real time, particularly: (i) real-time measurements of basic cancer cell metabolism of different cancer cell lines; (ii) a detailed timeline of the metabolic response to cisplatin treatment and clear detection of the time span between start of cisplatin treatment and onset of cell death, which reflects the time required for the underlying molecular mechanisms of cell fate decision; (iii) direct functional measurement of the biological activity of a key regulatory protein of cellular metabolism following the kinetic change in respiration upon SIRT3 overexpression; and (iv) the time-resolved impact of several organometallic compounds on cell metabolism and cell morphology, including unexpected and not yet understood highly significant and specific effects on cell-cell interaction and adhesion.
出版日期Book 2015
關(guān)鍵詞Biosensor Chip; Cancer Metabolism; Chemotherapeutic Drugs; Cisplatin; Real-Time Analysis
版次1
doihttps://doi.org/10.1007/978-3-658-10161-9
isbn_softcover978-3-658-10160-2
isbn_ebook978-3-658-10161-9
copyrightSpringer Fachmedien Wiesbaden 2015
The information of publication is updating

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Introduction,oval for clinical application regarding drug safety and target efficacy (Marx and Sandig 2007). Any potential candidate compound must pass several phases of clinical testing (Fig. 1.1). A major approach has been to use laboratory animals or animal models, but the screening of thousands of novel comp
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Results,ing lowest in MCF-7 and highest in HCT-116; respiration being highest in MCF-7 and lowest in HT-29. Differences in glycolytic and respiratory activity may reflect variations in a cell’s ability to react to severe stress conditions. For instance, the lower basic glycolytic rate in MCF-7 cells may all
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Discussion,231, the two colorectal cancer cell lines HT-29 and HCT-116, and the liver hepatocellular carcinoma HepG2). In particular, there is a pronounced difference in the levels of glycolysis and respiration between MCF-7 (lowest acidification and highest respiration rates) and the other employed cell lines
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