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| April 2016 Volume 16 Number 4 | Advertisement | |||||||||||||||||||||||||||||||||||||||||||||
| In this issue
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| REVIEWS | Top | |||||||||||||||||||||||||||||||||||||||||||||
| Targeting metastasis Patricia S. Steeg p201 | doi:10.1038/nrc.2016.25 Tumour metastasis is a major contributor to the mortality of cancer patients, so why is this phase of cancer pathogenesis not routinely targeted? This Review discusses the possible strategies — including preclinical research, combination therapies and clinical trial designs — that could be developed to target metastasis. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
| Vaccines for established cancer: overcoming the challenges posed by immune evasion Sjoerd H. van der Burg, Ramon Arens, Ferry Ossendorp, Thorbald van Hall & Cornelis J. M. Melief p219 | doi:10.1038/nrc.2016.16 This Review summarizes immune evasion mechanisms that limit the therapeutic efficacy of cancer vaccines. The authors discuss how improving vaccine design and using vaccines in combination with other anticancer therapies can boost treatment efficacy in patients with established cancers. Abstract | Full Text | PDF | Supplementary information | ||||||||||||||||||||||||||||||||||||||||||||||
| Radiation oncology in the era of precision medicine Michael Baumann, Mechthild Krause, Jens Overgaard, Jürgen Debus, Søren M. Bentzen, Juliane Daartz, Christian Richter, Daniel Zips & Thomas Bortfeld p234 | doi:10.1038/nrc.2016.18 This Review discusses technological and biologically based advances in radiotherapy. The authors envisage that these two major strategies will act synergistically to further widen the therapeutic window of radiation oncology in the era of precision medicine. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
| ANALYSIS | Top | |||||||||||||||||||||||||||||||||||||||||||||
| The importance of p53 pathway genetics in inherited and somatic cancer genomes Giovanni Stracquadanio, Xuting Wang, Marsha D. Wallace, Anna M. Grawenda, Ping Zhang, Juliet Hewitt, Jorge Zeron-Medina, Francesc Castro-Giner, Ian P. Tomlinson, Colin R. Goding, Kamil J. Cygan, William G. Fairbrother, Laurent F. Thomas, Pål Sætrom, Federica Gemignani, Stefano Landi, Benjamin Schuster-Böckler, Douglas A. Bell & Gareth L. Bond p251 | doi:10.1038/nrc.2016.15 Using genomic data, this Analysis demonstrates that commonly inherited single nucleotide polymorphisms (SNPs) occurring in genes of the p53 pathway affect the incidence of a broad range of cancers, more so than SNPs in other pathways. This has implications for p53-mediated tumour suppression in humans. Abstract | Full Text | PDF | Supplementary information | ||||||||||||||||||||||||||||||||||||||||||||||
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| PERSPECTIVES | Top | |||||||||||||||||||||||||||||||||||||||||||||
| OPINION Inducing stable reversion to achieve cancer control Scott Powers & Robert E. Pollack p266 | doi:10.1038/nrc.2016.12 Current cancer therapies exert selective pressures that drive the evolution of drug-resistant clones. In this Opinion article, the authors argue that induction of stable tumour reversion represents an alternative strategy that could reduce resistance and thus effectively and durably treat cancer. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||||
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| *2014 Journal Citation Report (Thomson Reuters, 2015) |
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