4.8 Article

Essentiality of fatty acid synthase in the 2D to anchorage-independent growth transition in transforming cells

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NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-13028-1

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资金

  1. Instituto de Salud Carlos III (ISCIII) [FIS PI13/00430, FIS PI16/00354, FIS PI11/00832, FIS PI14/00726]
  2. European Regional Development Fund (ERDF) [II14/00009]
  3. AECC Scientific Foundation (Beca de Retorno 2010)
  4. NIH [5R35CA197532]
  5. Ministerio de Economia y Competitividad (MINECO) [BFU2014-57466]
  6. MINECO [SAF2016-78114-R]
  7. Instituto de Salud Carlos III [RD12/0043/0021]
  8. Junta de Castilla y Leon (Escalera de Excelencia) [CLU-2017-03]
  9. Ayudas Equipos Investigacion Biomedicina 2017 Fundacion BBVA
  10. Fundacion Ramon Areces
  11. Ministerio de Sanidad, Spain [PIE15/00068]

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Upregulation of fatty acid synthase (FASN) is a common event in cancer, although its mechanistic and potential therapeutic roles are not completely understood. In this study, we establish a key role of FASN during transformation. FASN is required for eliciting the anaplerotic shift of the Krebs cycle observed in cancer cells. However, its main role is to consume acetyl-CoA, which unlocks isocitrate dehydrogenase (IDH)-dependent reductive carboxylation, producing the reductive power necessary to quench reactive oxygen species (ROS) originated during the switch from two-dimensional (2D) to three-dimensional (3D) growth (a necessary hallmark of cancer). Upregulation of FASN elicits the 2D-to-3D switch; however, FASN's synthetic product palmitate is dispensable for this process since cells satisfy their fatty acid requirements from the media. In vivo, genetic deletion or pharmacologic inhibition of FASN before oncogenic activation prevents tumor development and invasive growth. These results render FASN as a potential target for cancer prevention studies.

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