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      The Cancer Cell Map Initiative: Defining the Hallmark Networks of Cancer

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          Abstract

          Progress in DNA sequencing has revealed the startling complexity of cancer genomes, which typically carry thousands of somatic mutations. However, it remains unclear which are the key driver mutations or dependencies in a given cancer and how these influence pathogenesis and response to therapy. Although tumors of similar types and clinical outcomes can have patterns of mutations that are strikingly different, it is becoming apparent that these mutations recurrently hijack the same hallmark molecular pathways and networks. For this reason, it is likely that successful interpretation of cancer genomes will require comprehensive knowledge of the molecular networks under selective pressure in oncogenesis. Here we announce the creation of a new effort, called The Cancer Cell Map Initiative (CCMI), aimed at systematically detailing these complex interactions among cancer genes and how they differ between diseased and healthy states. We discuss recent progress that enables creation of these Cancer Cell Maps across a range of tumor types and how they can be used to target networks disrupted in individual patients, significantly accelerating the development of precision medicine.

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          Author and article information

          Journal
          9802571
          20730
          Mol Cell
          Mol. Cell
          Molecular cell
          1097-2765
          1097-4164
          10 February 2017
          21 May 2015
          20 March 2017
          : 58
          : 4
          : 690-698
          Affiliations
          [1 ]California Institute for Quantitative Biosciences (QB3), University of San Francisco at California, San Francisco, 94143
          [2 ]Department of Cellular and Molecular Pharmacology, University of San Francisco at California, San Francisco, 94143
          [3 ]J. David Gladstone Institutes, San Francisco, 94143
          [4 ]Helen Diller Comprehensive Cancer Center, University of California at San Francisco, San Francisco, California 94143
          [5 ]Department of Medicine, University of California at San Diego, San Diego, California, 92093
          [6 ]Moores Cancer Center, University of California at San Diego San Diego, California, 92093
          [7 ]Department of Biochemistry and Biophysics, University of California at San Francisco, San Francisco, California, 92093
          [8 ]Department of Medicine, University of California at San Francisco, San Francisco, California, 92093
          Author notes
          Article
          PMC5359018 PMC5359018 5359018 hhmipa850605
          10.1016/j.molcel.2015.05.008
          5359018
          26000852
          d777abc2-c021-494b-8144-5098859705f6
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