作者: Paul Workman , Paul A. Clarke , Bissan Al-Lazikani
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摘要: It is now recognised that genetic, epigenetic and phenotypic heterogeneity within individual human cancers responsible for therapeutic resistance - knowledge having a profound impact on current thinking experimentation. There has been concern molecularly targeted therapy doomed to failure, with resistant clones emerging in response the Darwinian selective pressure of any drug treatment. However, two studies have shown evolution can be restrained by co-administration pharmacologic inhibitor HSP90 molecular chaperone.