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| October 2015 Volume 15 Number 10 | Advertisement | |||||||||||||||||||||||||||||||||||||||||||||
| In this issue
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| REVIEWS | Top | |||||||||||||||||||||||||||||||||||||||||||||
| MEK1 and MEK2 inhibitors and cancer therapy: the long and winding road Christopher J. Caunt, Matthew J. Sale, Paul D. Smith & Simon J. Cook p577 | doi:10.1038/nrc4000 MEK1 and MEK2 have key roles in tumorigenesis and, therefore, represent promising targets for cancer therapy. This Review discusses the mechanisms of action of different inhibitors of MEK1 and MEK2, the mechanisms of resistance to these inhibitors and their current clinical progress. Abstract | Full Text | PDF | Supplementary information | ||||||||||||||||||||||||||||||||||||||||||||||
| MYC: connecting selective transcriptional control to global RNA production Theresia R. Kress, Arianna Sabo & Bruno Amati p593 | doi:10.1038/nrc3984 The transcription factor MYC upregulates and downregulates distinct sets of target genes, promoting cell growth and proliferation, increased metabolic rate and RNA biogenesis. This Review discusses MYC-mediated transcriptional regulation in normal growth control, as well as in tumour development and maintenance. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
| The multifaceted functions of sirtuins in cancer Angeliki Chalkiadaki & Leonard Guarente p608 | doi:10.1038/nrc3985 This Review discusses the roles of members of the sirtuin (SIRT) family in cancer biology, which have dichotomous, context-dependent functions as tumour suppressors and oncogenes. Furthermore, the authors discuss the possibility of targeting the sirtuins for anticancer therapy. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
| PERSPECTIVES | Top | |||||||||||||||||||||||||||||||||||||||||||||
| OPINION Constitutional epimutation as a mechanism for cancer causality and heritability? Megan P. Hitchins p625 | doi:10.1038/nrc4001 Aberrations in gene expression due to an altered epigenotype that is widely distributed in normal tissues are referred to as constitutional epimutations. This Opinion article discusses the potential contribution of constitutional epimutations to the 'missing' causality and heritability of cancer. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
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| *2013 Journal Citation Report (Thomson Reuters, 2014) |
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