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      Understanding the intersections between metabolism and cancer biology

      research-article
      1 , 2 , 3 , 4 , 5
      Cell

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          Abstract

          Transformed cells adapt metabolism to support tumor initiation and progression. Specific metabolic activities can participate directly in the process of transformation or support the biological processes that enable tumor growth. Exploiting cancer metabolism for clinical benefit requires defining the pathways that are limiting for cancer progression and understanding the context specificity of metabolic preferences and liabilities in malignant cells. Progress towards answering these questions is providing new insight into cancer biology and can guide the more effective targeting of metabolism to help patients.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          4 February 2017
          09 February 2017
          09 February 2018
          : 168
          : 4
          : 657-669
          Affiliations
          [1 ]The Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
          [2 ]Dana–Farber Cancer Institute, Boston, Massachusetts 02115, USA
          [3 ]Children’s Medical Center Research Institute, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [4 ]Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [5 ]Eugene McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          Author notes
          [* ]Contacts: mvh@ 123456mit.edu , 77 Massachusetts Avenue, 76-561, Cambridge, MA 02139, Tel: 617-715-4471 Fax: 617-258-6558, ralph.deberardinis@ 123456utsouthwestern.edu , 5323 Harry Hines Blvd, Room NL12.138B, Dallas, TX 75390-8502, Tel: 214-648-2587 Fax: 214-648-5515
          Article
          PMC5329766 PMC5329766 5329766 nihpa848132
          10.1016/j.cell.2016.12.039
          5329766
          28187287
          ca288a10-86c3-44d8-a4e0-da195330cde5
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