Table of contents


From the editors

p565 | doi:10.1038/nrc2203

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Research Highlights

Microenvironment: A disturbed background | PDF (307 KB)

p566 | doi:10.1038/nrc2194

Genetics: Common ground | PDF (180 KB)

p567 | doi:10.1038/nrc2195

In the news

FDA squashes tomato anticancer claims | PDF (66 KB)

p567 | doi:10.1038/nrc2207

Breast cancer: X-linked tumour suppression | PDF (167 KB)

p568 | doi:10.1038/nrc2200

Signalling: Expression levels are not as they appear | PDF (219 KB)

p568 | doi:10.1038/nrc2201

Tumorigenesis: Innate response | PDF (138 KB)

p568 | doi:10.1038/nrc2206

Trial Watch

| PDF (78 KB)

p569 | doi:10.1038/nrc2204

Breast cancer: A useful combination | PDF (115 KB)

p570 | doi:10.1038/nrc2197

Targeting: Intra-fering with interactions | PDF (157 KB)

p570 | doi:10.1038/nrc2198

Angiogenesis: Hidden signatures written in blood | PDF (126 KB)

p571 | doi:10.1038/nrc2199

Immune tolerance: New mechanism of tolerance induction in cancer | PDF (147 KB)

p572 | doi:10.1038/nrc2202

In brief

| PDF (90 KB)

p572 | doi:10.1038/nrc2205

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Reviews

See also: Correspondence by Cavaletti | Correspondence by Kelland

The resurgence of platinum-based cancer chemotherapy

Lloyd Kelland

p573 | doi:10.1038/nrc2167

Cisplatin was first used for cancer therapy in the 1970s. Interest in platinum drugs has been revived recently: new agents have been developed, a better understanding of resistance mechanisms has been gained, and combination trials with resistance modulators and targeted agents have been initiated.

Understanding multiple myeloma pathogenesis in the bone marrow to identify new therapeutic targets

Teru Hideshima, Constantine Mitsiades, Giovanni Tonon, Paul G. Richardson & Kenneth C. Anderson

p585 | doi:10.1038/nrc2189

Multiple myeloma is an incurable B-cell malignancy that is actively sustained by the bone marrow microenvironment. Targeting myeloma cells and their bone marrow interactions seems a promising strategy to overcome drug resistance and improve patient outcome.

Molecular mechanisms of alcohol-mediated carcinogenesis

Helmut K. Seitz & Felix Stickel

p599 | doi:10.1038/nrc2191

Alcohol is one of the most widely consumed toxic substances, and approxmiately 3.6% of cancers result from chronic alcohol drinking. What are some of the mechanisms by which alcohol acts as a carcinogen?

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Perspectives

Innovation

Active-site directed probes to report enzymatic action in the ubiquitin proteasome system

Huib Ovaa

p613 | doi:10.1038/nrc2128

Irreversible covalent inhibitors equipped with reporter groups allow the study of target enzymes based on catalytic activity instead of expression level. This Perspective discusses the design and use of such probes directed at the ubiquitin–proteasome system. Can they identify new cancer therapies that target this system?

Opinion

Treating prostate cancer: a rationale for targeting local oestrogens

Stuart J. Ellem & Gail P. Risbridger

p621 | doi:10.1038/nrc2174

A role for oestrogen has been implicated in the development of prostate cancer, but this role is complex. Should selective oestrogen-receptor modulators in conjunction with contemporary androgen-ablation therapy be used to treat this disease?

Opinion

The disappearing Barr body in breast and ovarian cancers

Gayle J. Pageau, Lisa L. Hall, Shridar Ganesan, David M. Livingston & Jeanne B. Lawrence

p628 | doi:10.1038/nrc2172

This article examines whether heterochromatic instability might explain the loss of the heterochromatic inactive X chromosome (Barr body) in some breast and ovarian cancers. Might this mechanism have wider implications for the evolution of some cancer types?

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