Friday, May 22, 2015

Nature Reviews Cancer contents June 2015 Volume 15 Number 6 pp317-381

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Nature Reviews Cancer


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TABLE OF CONTENTS
 
June 2015 Volume 15 Number 6
Nature Reviews Cancer cover
Impact Factor 37.912 *
In this issue
Research Highlights
Reviews
Perspectives

Also this month
 Featured article:
MicroRNA biogenesis pathways in cancer
Shuibin Lin & Richard I. Gregory


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RESEARCH HIGHLIGHTS
Top

Drug delivery: Get in there!
p317 | doi:10.1038/nrc3963
Two different devices have been developed to deliver cancer drugs directly into tumours in vivo to evaluate cell penetration, drug stability and effectiveness.
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Colorectal cancer: A circuitous way to target p53
p318 | doi:10.1038/nrc3962
Liu et al. show that the mushroom-derived toxin α-amanitin, conjugated to antibodies against a tumour-specific biomarker, might be effective therapeutically (with minimal toxicity) for tumours that have hemizygous deletions of TP53 that also encompass POLR2A.
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Therapeutic resistance: Fibroblasts restrain drug sensitivity
p318 | doi:10.1038/nrc3965
Hirata et al. used intravital imaging to characterize a surprising form of BRAF-V600E inhibitor resistance in melanoma.
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Immunotherapy: Put your coat on!
p319 | doi:10.1038/nrc3964
Tumour cells coated with immunoglobulin G are able to induce an immune response in mice that causes tumour regression.
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Non-coding RNA: Stressed to bits
p320 | doi:10.1038/nrc3966
Goodarzi et al. find that small non-coding RNAs derived from the cleavage of tRNAs under hypoxic conditions can suppress metastatic progression.
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IN BRIEF

Immunotherapy: Killer combo | Tumour immunology: Eosinophils — T cells' little helpers | Metabolism: Bacterial biofilms may feed colon cancer
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REVIEWS
Top
MicroRNA biogenesis pathways in cancer
Shuibin Lin & Richard I. Gregory
p321 | doi:10.1038/nrc3932
The microRNA (miRNA) biogenesis pathway is frequently altered in cancer, leading to global downregulation of miRNA levels in some cancer types. This Review discusses the alterations that affect miRNA biogenesis in cancer.
Abstract | Full Text | PDF | Supplementary information

Hijacked in cancer: the KMT2 (MLL) family of methyltransferases
Rajesh C. Rao & Yali Dou
p334 | doi:10.1038/nrc3929
Histone-lysine N-methyltransferase 2 (KMT2) family proteins, initially named the mixed lineage leukaemia (MLL) family, are altered in many types of cancers beyond MLL. Inhibitors of KMT2 function are being developed and could work as therapeutics in a variety of cancer types.
Abstract | Full Text | PDF

Radioimmunotherapy of human tumours
Steven M. Larson, Jorge A. Carrasquillo, Nai-Kong V. Cheung & Oliver W. Press
p347 | doi:10.1038/nrc3925
The modern manufacture of tumour-selective antibodies bearing tumour-killing radioactive cargo has effectively harnessed the power of the atom to safely destroy cancer cells. This Review presents fundamental concepts of chemistry, physics and biology that are essential for the effective radioimmunotherapy of human cancer.
Abstract | Full Text | PDF | Supplementary information

Building better monoclonal antibody-based therapeutics
George J. Weiner
p361 | doi:10.1038/nrc3930
How can we improve the design of monoclonal antibodies (mAbs) to treat cancer? In this Review, George J. Weiner discusses the characteristics of mAbs that can affect their efficacy, the current approaches that use mAbs in cancer treatment and the numerous ways to enhance the potential of these mAb-based techniques.
Abstract | Full Text | PDF

 
PERSPECTIVES
Top
TIMELINE
The emerging complexity of gene fusions in cancer
Fredrik Mertens, Bertil Johansson, Thoas Fioretos & Felix Mitelman
p371 | doi:10.1038/nrc3947
Since the Philadelphia chromosome was discovered in 1960, studies over the past six decades have identified fusion genes, oncogenes that provide great diagnostic and therapeutic advantages because of their tumour-specific expression. This Timeline article revisits the spectrum of gene fusions in cancer and how the methods to identify them have evolved, and also discusses the implications of current, sequencing-based approaches for detection.
Abstract | Full Text | PDF | Supplementary information

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