Table of contents


In this issue

p765 | doi:10.1038/nrd2439

Editorial: Dealing with a data deficit

p767 | doi:10.1038/nrd2440

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Research Highlights

Drug metabolism: Production line for hepatocytes | PDF (333 KB)

p781 | doi:10.1038/nrd2427

Cardiovascular disease: Reducing the pressure | PDF (357 KB)

p782 | doi:10.1038/nrd2426

Anticancer drugs: Forecasting drug responses | PDF (186 KB)

p782 | doi:10.1038/nrd2429

Cytokine hormones: Designed to linger | PDF (401 KB)

p783 | doi:10.1038/nrd2430

RNA interference: Targeted knockdown | PDF (133 KB)

p784 | doi:10.1038/nrd2428

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Perspectives

Opinion

Growth of the Asian health-care market: global implications for the pharmaceutical industry

Richard J. Epstein

p785 | doi:10.1038/nrd2360

The digital information revolution has led to the rapid development of many countries, causing the pharmaceutical industry to face a new array of Asia-specific challenges. Epstein discusses how understanding Asia's diverse cultures, talents and markets will bring about success for the industry.

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Reviews

RAR and RXR modulation in cancer and metabolic disease

Lucia Altucci, Mark D. Leibowitz, Kathleen M. Ogilvie, Angel R. de Lera & Hinrich Gronemeyer

p793 | doi:10.1038/nrd2397

Retinoic acid receptors (RARs) are ligand-controlled transcription factors that function as heterodimers with retinoid X receptors (RXRs) to regulate cell growth and survival. This article discusses recent advances in the understanding of the biological role of RARs and RXRs and their implications for the design of selective receptor modulators for cancer and metabolic diseases.

Design of selective nuclear receptor modulators: RAR and RXR as a case study

Angel R. de Lera, William Bourguet, Lucia Altucci & Hinrich Gronemeyer

p811 | doi:10.1038/nrd2398

Retinoic acid receptors (RARs) are important drug targets for cancer therapy and prevention, and the potential of rexinoids for the treatment of metabolic diseases is increasingly being recognized. This article reviews recent structural data for RARs and retinoid X receptors (RXRs), discusses strategies in the design of selective RXR and RAR modulators, and consider lessons that can be learned for the design of selective nuclear-receptor modulators in general.

Modifying IGF1 activity: an approach to treat endocrine disorders, atherosclerosis and cancer

David R. Clemmons

p821 | doi:10.1038/nrd2359

In this Review, Clemmons discusses how strategies to utilize IGF1's growth stimulating and anabolic properties are being pursued to treat short stature, catabolism and diabetes, and highlights the potential benefit of IGF1 antagonism in cancer therapy.

Flying under the radar: the new wave of BCR–ABL inhibitors

Alfonso Quintás-Cardama, Hagop Kantarjian & Jorge Cortes

p834 | doi:10.1038/nrd2324

Chronic myeloid leukaemia caused by the mutant BCR–ABL kinase has been successfully treated with inhibitors of this kinase, such as imatinib, but mutations within the kinase can result in resistance to these drugs. Quintás-Cardama and colleagues discuss novel BCR–ABL inhibitors that have the potential to overcome such resistance.

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Careers and Recruitment

Tools and technologies

p849 | doi:10.1038/nrd2432

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