Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
In the past few years, researchers have reported dramatic responses to a handful of new drugs that are given to cancer patients with a specific mutation in their tumors. But although these drugs can shrink solid tumors and extend patients' lives, for reasons that are still not well understood, they never completely eliminate the cancer. Researchers are seeking to identify the ways that tumors resist the drug, then find or develop second-generation drugs that block these escape routes so they can design a cocktail—perhaps two, three, or more drugs—that, if given when a patient is first diagnosed, could stop tumors from ever evading the blockade. This approach has worked for patients infected with HIV, who usually take three antiviral drugs, and many researchers say there's no reason it shouldn't work for cancer. But even if a combination therapy stops tumor growth, it may not buy patients more than a temporary reprieve, researchers admit. To stretch the benefit over years, it might be necessary to devise one complex cocktail after another, each tailored to a patient's evolving tumors.
The editors suggest the following Related Resources on Science sites:
In Science Magazine
INTRODUCTION TO SPECIAL ISSUE
Paula Kiberstis and Eliot Marshall (25 March 2011) Science331 (6024), 1539-a.
[DOI: 10.1126/science.331.6024.1539-a] |Full Text »|PDF »
In Science Signaling
RESEARCH ARTICLES
Annette S. Little, Kathryn Balmanno, Matthew J. Sale, Scott Newman, Jonathan R. Dry, Mark Hampson, Paul A. W. Edwards, Paul D. Smith, and Simon J. Cook (29 March 2011) Sci. Signal.4 (166), ra17.
[DOI: 10.1126/scisignal.2001752] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
PERSPECTIVES
Poulikos I. Poulikakos and David B. Solit (29 March 2011) Sci. Signal.4 (166), pe16.
[DOI: 10.1126/scisignal.2001948] |Abstract »|Full Text »|PDF »
EDITORIAL GUIDES
Elizabeth M. Adler and Nancy R. Gough (29 March 2011) Sci. Signal.4 (166), eg3.
[DOI: 10.1126/scisignal.2002014] |Abstract »|Full Text »|PDF »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Conquering Cancer in Our Lifetime: New Diagnostic and Therapeutic Trends.
E. P. Diamandis, R. C. Bast Jr., and C. Lopez-Otin (2013)
Clin. Chem.
59, 1-3
|Full Text »|PDF »
Network-based drug discovery by integrating systems biology and computational technologies.
E. L. Leung, Z.-W. Cao, Z.-H. Jiang, H. Zhou, and L. Liu (2012)
Brief Bioinform
|Abstract »|Full Text »|PDF »
Electron transfer-based combination therapy of cisplatin with tetramethyl-p-phenylenediamine for ovarian, cervical, and lung cancers.
T. Luo, J. Yu, J. Nguyen, C.-R. Wang, R. G. Bristow, D. A. Jaffray, X. Z. Zhou, K. P. Lu, and Q.-B. Lu (2012)
PNAS
109, 10175-10180
|Abstract »|Full Text »|PDF »
Cancer drug pan-resistance: pumps, cancer stem cells, quiescence, epithelial to mesenchymal transition, blocked cell death pathways, persisters or what?.