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The ectopic expression of mutant variants of PTEN, which are either devoid of lipid phosphatase (G129E) or both lipid and protein phosphatase (C124S) activity, results in a reduction in doxorubicin sensitivity in MCF-7 cells with wild-type PTEN while simultaneously increasing sensitivity to the mTOR inhibitor, rapamycin [37]
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Phase I and pharmacologic study of the human DNA methyltransferase antisense oligodeoxynucleotide MG98 given as a 21-day continuous infusion every 4 weeks
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