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AKT as locus of cancer multidrug resistance and fragility

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JOURNAL OF CELLULAR PHYSIOLOGY
卷 228, 期 4, 页码 671-674

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WILEY
DOI: 10.1002/jcp.24176

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  1. Yad Chessed Foundation

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Complexity and robustness of cancer hypoxic microenvironment are supported by the robust signaling networks of autocrine and paracrine elements creating powerful interactome for multidrug resistance. These elements generate a positive feedback loops responsible for the extreme robustness and multidrug resistance in solid cancer, leukemia, myeloma, and lymphoma. Phosphorylated AKT is a cancer multidrug resistance locus. Targeting that locus by oxidant/antioxidant balance modulation, positive feedback loops are converted into negative feedback loops, leading to disappearance of multidrug resistance. This is a new principle for targeting cancer multidrug resistance by the locus chemotherapy inducing a phenomenon of loops conversion. J. Cell. Physiol. 228: 671674, 2013. (c) 2012 Wiley Periodicals, Inc.

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