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      <dc:title>Therapeutic targeting of glutaminolysis as an essential strategy to combat cancer</dc:title>
      <dc:creator>Mates-Sánchez, José Manuel</dc:creator>
      <dc:creator>di Paola, Floriana J.</dc:creator>
      <dc:creator>Campos-Sandoval, José Ángel</dc:creator>
      <dc:creator>Mazurek, Sybille</dc:creator>
      <dc:creator>Márquez-Gómez, Javier</dc:creator>
      <dc:subject>Cáncer</dc:subject>
      <dc:description>Metabolic reprogramming in cancer targets glutamine metabolism as a key mechanism to provide energy,&#xd;
biosynthetic precursors and redox requirements to allow the massive proliferation of tumor cells. Glutamine is&#xd;
also a signaling molecule involved in essential pathways regulated by oncogenes and tumor suppressor factors.&#xd;
Glutaminase isoenzymes are critical proteins to control glutaminolysis, a key metabolic pathway for cell proliferation&#xd;
and survival that directs neoplasms’ fate. Adaptive glutamine metabolism can be altered by different&#xd;
metabolic therapies, including the use of specific allosteric inhibitors of glutaminase that can evoke synergistic&#xd;
effects for the therapy of cancer patients. We also review other clinical applications of in vivo assessment of&#xd;
glutaminolysis by metabolomic approaches, including diagnosis and monitoring of cancer.</dc:description>
      <dc:date>2024-09-23T09:20:11Z</dc:date>
      <dc:date>2024-09-23T09:20:11Z</dc:date>
      <dc:date>2024-09-18</dc:date>
      <dc:date>2020-02</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>José M. Matés, Floriana J. Di Paola, José A. Campos-Sandoval, Sybille Mazurek, Javier Márquez, Therapeutic targeting of glutaminolysis as an essential strategy to combat cancer, Seminars in Cell &amp; Developmental Biology, Volume 98, 2020, Pages 34-43, ISSN 1084-9521, https://doi.org/10.1016/j.semcdb.2019.05.012. (https://www.sciencedirect.com/science/article/pii/S1084952119300734)</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/32822</dc:identifier>
      <dc:identifier>10.1016/j.semcdb.2019.05.012</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
      <dc:publisher>Elsevier</dc:publisher>
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