Table of contents


From the editors

p653 | doi:10.1038/nrc1990

Top

Research Highlights

Targeted therapy: Stressed out hearts

p655 | doi:10.1038/nrc1980

Tumorigenesis: Decidedly different

p656 | doi:10.1038/nrc1981

In the news

In the news

p656 | doi:10.1038/nrc1987

Anticancer agents: Digging in

p657 | doi:10.1038/nrc1960

Tumour transmission: Transmission possible

p657 | doi:10.1038/nrc1983

Metastasis: Anger management

p658 | doi:10.1038/nrc1985

Tumorigenesis: Stress and cancer

p658 | doi:10.1038/nrc1986

Targeted therapies: The next move

p659 | doi:10.1038/nrc1988

Signalling: Eph-ective tumour growth inhibition

p660 | doi:10.1038/nrc1978

Pharmacodynamics: A new model

p660 | doi:10.1038/nrc1982

Therapy: Through the barricades

p660 | doi:10.1038/nrc1984

In brief

Angiogenesis | Tumour suppressors | Metastasis | Cell death

p661 | doi:10.1038/nrc1989

Top

Reviews

Divorcing ARF and p53: an unsettled case

Charles J. Sherr

p663 | doi:10.1038/nrc1954

The ARF tumour suppressor can activate p53-dependent transcriptional pathways by inhibiting the ubiquitin ligase MDM2. However, ARF has been reported to have p53-independent activities. How important are these activities in tumorigenesis? This Review critically appraises the current data.

Hepatocellular carcinoma pathogenesis: from genes to environment

Paraskevi A. Farazi & Ronald A. DePinho

p674 | doi:10.1038/nrc1934

Hepatocellular carcinoma (HCC) is highly lethal and has a high incidence worldwide. However, at present there is only a basic understanding of the genetic, cellular and environmental mechanisms that drive HCC pathogenesis. What is known, and what are the challenges and opportunities?

Polymer conjugates as anticancer nanomedicines

Ruth Duncan

p688 | doi:10.1038/nrc1958

Polymers can be conjugated to anticancer drugs and proteins to improve their therapeutic index. Some such conjugates are in routine clinical use and there are exciting advances in development, such as polymer-based combination therapies.

Preventing or reducing late side effects of radiation therapy: radiobiology meets molecular pathology

Søren M. Bentzen

p702 | doi:10.1038/nrc1950

Progress in molecular radiobiology has improved the understanding of the pathogenesis of side effects that develop months or years after radiotherapy has been completed. This knowledge will help to improve the therapeutic efficacy of radiotherapy and the quality of life of long-term cancer survivors.

Comparing antibody and small-molecule therapies for cancer

Kohzoh Imai & Akinori Takaoka

p714 | doi:10.1038/nrc1913

Several small-molecule inhibitors and monoclonal antibodies are now approved for the therapy of various cancers. Focusing on the example of the epidermal growth factor receptor inhibitors, this Review compares and contrasts these two classes of agents.

Top

Perspectives

Opinion

mTOR and cancer: insights into a complex relationship

David M. Sabatini

p729 | doi:10.1038/nrc1974

Drugs that target mTOR (mammalian target of rapamycin) have entered clinical trials for cancer treatment. However, current mTOR inhibitors have an unexpectedly complex mechanism of action. Can our emerging knowledge of this pathway be used to develop more effective mTOR-targeted therapies?

Opinion

Linking oncogenic pathways with therapeutic opportunities

Andrea H. Bild, Anil Potti & Joseph R. Nevins

p735 | doi:10.1038/nrc1976

Multiple mutations and alterations in the cancer genome lead to the deregulation of various cell-signalling pathways that control cell function. Can molecular-profiling studies be used to fully understand this complexity and provide an opportunity to link pathway deregulation with potential therapeutic strategies?

Corrigendum: Drug interactions in cancer therapy

Charity D. Scripture & William D. Figg

p741 | doi:10.1038/nrc1975

Erratum: Lineage dependency and lineage-survival oncogenes in human cancer

Levi A. Garraway & William R. Sellers

p742 | doi:10.1038/nrc1972

Erratum: Targeting the mechanisms of tumoral immune tolerance with small-molecule inhibitors

Alexander J. Muller & Peggy A. Scherle

p742 | doi:10.1038/nrc1979

Extra navigation

Subscribe

Subscribe to Nature Reviews Cancer

naturejobs

natureproducts


Advertisement