Friday, October 24, 2014

Nature Reviews Cancer contents November 2014 Volume 14 Number 11 pp701-762

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Nature Reviews Cancer


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TABLE OF CONTENTS
 
November 2014 Volume 14 Number 11Advertisement
Nature Reviews Cancer cover
Impact Factor 37.912 *
In this issue
Comment
Research Highlights
Reviews
Perspectives

Also this month
Article series:
Clinical insights
Featured article:
Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel?
Simran S. Sabharwal & Paul T. Schumacker

 
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Article series: Clinical insights
Comment: Shouldn't we care about the biology of benign tumours?
Adrian Marino-Enriquez & Christopher D. M. Fletcher
p701 | doi:10.1038/nrc3845
This Comment article argues that we should more comprehensively study the biology of benign tumours, as this might provide crucial insights into our understanding of cancer biology and metastasis.
Abstract | Full Text | PDF | Supplementary information

RESEARCH HIGHLIGHTS
Top

Metastasis: Metabolic reprogramming in disseminated cells
p703 | doi:10.1038/nrc3842
LeBleu et al. show that the metabolism of migratory and circulating tumour cells is different to that of primary tumour cells and this difference enables migration and metastasis.
PDF


Angiogenesis: Pushing through, branching out
p704 | doi:10.1038/nrc3841
Blood vessel branching during tumour angiogenesis is mediated by the formation of podosome rosettes.
PDF


Microenvironment: Source influences function
p704 | doi:10.1038/nrc3843
Several tumour-promoting roles of cathepsin Z (CTSZ) in pancreatic neuroendocrine tumours (PanNETs) depend on its RGD motif, and CTSZ derived from tumour cells or tumour-associated macrophages has different functions.
PDF


Leukaemia: Fine-tuning metabolism
p705 | doi:10.1038/nrc3839
Wang et al. show differential requirements for the glycolytic enzymes pyruvate kinase M2 and lactate dehydrogenase A in maintaining haematopoietic stem cells and progenitor cells. Although this difference does not seem to apply to leukaemias derived from these two different cell populations, leukaemia cells are more sensitive to glycolysis inhibition than normal cells.
PDF


Metabolism: Reprogramming metabolic flux in glioma
p706 | doi:10.1038/nrc3840
Chen et al. have shown that growth of isocitrate dehydrogenase 1 (IDH1)-mutant gliomas is promoted by expression of glutamate dehydrogenase 2 (GLUD2) protein.
PDF


Tumorigenesis: Establishing the origin of retinoblastoma
p706 | doi:10.1038/nrc3849
Xu et al. have identified the cell of origin of retinoblastoma and the cell type-specific circuitry that these tumour cells rely on.
PDF



IN BRIEF

Tumorigenesis: BOC's plot thickens | Therapeutics: Delivered in a tea bag | Imaging: Marking the boundaries | Proteomics: Follow your heat | Genomic instability: SPRTN links cancer and ageing | Pancreatic cancer: Stromal modulation to prevent resistance | Lymphoma: Release the B cell | Tumorigenesis: Why melanoma?
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Cancer
JOBS of the week
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Cancer Research UK Manchester Institute
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Goethe-Universität Frankfurt am Main
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REVIEWS
Top
Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel?
Simran S. Sabharwal & Paul T. Schumacker
p709 | doi:10.1038/nrc3803
Reactive oxygen species (ROS) are generated through various mechanisms. Accumulating evidence indicates that these moieties have important roles in promoting tumorigenesis and tumour progression; modulating the redox balance could be a strategy in targeting cancer.
Abstract | Full Text | PDF

Translational biology of osteosarcoma
Maya Kansara, Michele W. Teng, Mark J. Smyth & David M. Thomas
p722 | doi:10.1038/nrc3838
Survival for patients with metastatic or relapsed osteosarcoma has remained virtually unchanged during the past 30 years, and new therapeutic options are needed. This Review discusses normal bone biology relevant to osteosarcoma, including the immunobiology of bone, model systems for studying osteosarcoma, genetic and genomic studies on germline predisposition and tumour landscapes, and recent clinical trials.
Abstract | Full Text | PDF | Supplementary information

Revisiting STAT3 signalling in cancer: new and unexpected biological functions
Hua Yu, Heehyoung Lee, Andreas Herrmann, Ralf Buettner & Richard Jove
p736 | doi:10.1038/nrc3818
The Janus kinases (JAKs) are major activators of signal transducer and activator of transcription (STAT) proteins, and this signalling axis is crucial for cancer development in both tumour cells and the tumour microenvironment. This Review discusses the new roles of JAK-STAT signalling in promoting cancer through inflammation, obesity, stem cells and the pre-metastatic niche, and the potential therapeutic strategies that these roles can offer.
Abstract | Full Text | PDF

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PERSPECTIVES
Top
OPINION
Poised epigenetic states and acquired drug resistance in cancer
Robert Brown, Edward Curry, Luca Magnani, Charlotte S. Wilhelm-Benartzi & Jane Borley
p747 | doi:10.1038/nrc3819
Brown et al. argue that epigenetic heterogeneity leads to therapeutic resistance, such that bivalently marked gene promoters result in epigenetically poised gene expression that can become fixed by exposure to therapy. What are the opportunities to target this proposed mechanism of therapeutic resistance?
Abstract | Full Text | PDF | Supplementary information

OPINION
Cancer cachexia: understanding the molecular basis
Josep M. Argilés, Sílvia Busquets, Britta Stemmler & Francisco J. López-Soriano
p754 | doi:10.1038/nrc3829
Cancer cachexia is a multifactorial syndrome that affects many cancer patients and that leads to substantial weight loss, primarily from loss of skeletal muscle and body fat. This Opinion article focuses on the molecular mechanisms underlying cancer cachexia, in hopes that a better understanding of these might lead to improved therapeutic approaches.
Abstract | Full Text | PDF

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