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Dysregulated metabolism contributes to oncogenesis

  • Target Validation Team
  • Duke University Medical Center
  • University of Texas Southwestern Medical Center
  • University of Aberdeen
  • MRC Cancer Unit
  • Memorial Sloan Kettering Cancer Center
  • University of Maryland, Baltimore (UMB)
  • Johns Hopkins University School of Medicine
  • Rutgers University
  • Cornell University
  • University of Southern California
  • University of Michigan, Ann Arbor
  • Massachusetts Institute of Technology
  • Harvard Medical School
  • MRC Mitochondrial Biology Unit
  • Johns Hopkins University
  • Istituto Giannina Gaslini
  • University of Pennsylvania
  • Dana-Farber Cancer Institute
  • University of Florence
  • United Arab Emirates University
  • Wayne State University
  • Vellore Institute of Technology
  • University of Glasgow
  • Creighton University
  • Ovarian and Prostate Cancer Research Trust Laboratory
  • Nara Medical University
  • National Technical University of Athens
  • SASTRA University
  • New York Medical College
  • University of Illinois at Urbana - Champaign
  • Purdue University
  • Mayo Graduate School

Research output: Contribution to journalReview articlepeer-review

257 Scopus citations

Abstract

Cancer is a disease characterized by unrestrained cellular proliferation. In order to sustain growth, cancer cells undergo a complex metabolic rearrangement characterized by changes in metabolic pathways involved in energy production and biosynthetic processes. The relevance of the metabolic transformation of cancer cells has been recently included in the updated version of the review "Hallmarks of Cancer", where dysregulation of cellular metabolism was included as an emerging hallmark. While several lines of evidence suggest that metabolic rewiring is orchestrated by the concerted action of oncogenes and tumor suppressor genes, in some circumstances altered metabolism can play a primary role in oncogenesis. Recently, mutations of cytosolic and mitochondrial enzymes involved in key metabolic pathways have been associated with hereditary and sporadic forms of cancer. Together, these results demonstrate that aberrant metabolism, once seen just as an epiphenomenon of oncogenic reprogramming, plays a key role in oncogenesis with the power to control both genetic and epigenetic events in cells. In this review, we discuss the relationship between metabolism and cancer, as part of a larger effort to identify a broad-spectrum of therapeutic approaches. We focus on major alterations in nutrient metabolism and the emerging link between metabolism and epigenetics. Finally, we discuss potential strategies to manipulate metabolism in cancer and tradeoffs that should be considered. More research on the suite of metabolic alterations in cancer holds the potential to discover novel approaches to treat it.

Original languageBritish English
Pages (from-to)S129-S150
JournalSeminars in Cancer Biology
Volume35
DOIs
StatePublished - 1 Dec 2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cancer metabolism
  • Cancer therapy
  • Host metabolism
  • Mitochondria
  • Warburg

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