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      Metabolic heterogeneity in human lung tumors

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          SUMMARY

          Non-small cell lung cancer (NSCLC) is heterogeneous in the genetic and environmental parameters that influence cell metabolism in culture. Here, we assessed the impact of these factors on human NSCLC metabolism in vivo using intra-operative 13C-glucose infusions in nine NSCLC patients to compare metabolism between tumors and benign lung. While enhanced glycolysis and glucose oxidation were common among these tumors, we observed evidence for oxidation of multiple nutrients in each of them, including lactate as a potential carbon source. Moreover, metabolically heterogeneous regions were identified within and between tumors, and surprisingly, our data suggested potential contributions of non-glucose nutrients in well-perfused tumor areas. Our findings not only demonstrate the heterogeneity in tumor metabolism in vivo but also highlight the strong influence of the microenvironment on this feature.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          30 December 2015
          04 February 2016
          11 February 2016
          11 February 2017
          : 164
          : 4
          : 681-694
          Affiliations
          [1 ]Children’s Medical Center Research Institute, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [2 ]Department of Radiology, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [3 ]Advanced Imaging Research Center, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [4 ]Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [5 ]Clinical Research Office, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [6 ]Department of Cell Biology, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [7 ]Department of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [8 ]Department of Cardiovascular and Thoracic Surgery, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [9 ]Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [10 ]Eugene McDermott Center for Human Growth and Development, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA
          [11 ]Hadassah Medical Center, Jerusalem, Israel
          [12 ]Office of Animal Welfare Assurance, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA
          Author notes
          [* ]Contact: Ralph.deberardinis@ 123456utsouthwestern.edu , 5323 Harry Hines Blvd, Room NL12.138B, Dallas, TX 75390-8502. Tel: 214-648-2587. Fax: 214-648-5515
          Article
          PMC4752889 PMC4752889 4752889 nihpa747747
          10.1016/j.cell.2015.12.034
          4752889
          26853473
          d1166203-7401-45b1-85a2-f08218e4323f
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