Mithramycin Inhibits Etoposide Resistance in Glucose-deprived HT-29 Human Colon Carcinoma Cells

Physiological cell conditions such as glucose deprivation and hypoxia play roles in the development of drug resistance in solid tumors. These tumor-specific conditions cause decreased expression of DNA topoisomerase Ⅱα, rendering cells resistant to topo Ⅱ target drugs such as etoposide. Thus, target...

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Veröffentlicht in:Journal of microbiology and biotechnology 2007-11, Vol.17 (11), p.1856-1861
Hauptverfasser: Lee, E.M. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Park, H.R. (Kyungnam University, Masan, Republic of Korea), Hwang, J.H. (Kyungnam University, Masan, Republic of Korea), Park, D.J. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Chang, K.S. (Chungnam National University, Daejeon, Republic of Korea), Kim, C.J. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), E-mail: changjin@kribb.re.kr
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Sprache:eng
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Zusammenfassung:Physiological cell conditions such as glucose deprivation and hypoxia play roles in the development of drug resistance in solid tumors. These tumor-specific conditions cause decreased expression of DNA topoisomerase Ⅱα, rendering cells resistant to topo Ⅱ target drugs such as etoposide. Thus, targeting tumor-specific conditions such as a low glucose environment may be a novel strategy in the development of anticancer drugs. On this basis, we established a novel screening program for anticancer agents with preferential cytotoxic activity in cancer cells under glucose-deprived conditions.
ISSN:1017-7825