Dysregulated metabolism contributes to oncogenesis

被引:227
作者
Hirschey, Matthew D. [1 ,2 ,3 ]
DeBerardinis, Ralph J. [4 ]
Diehl, Anna Mae E. [1 ]
Drew, Janice E. [5 ]
Frezza, Christian [6 ]
Green, Michelle F.
Jones, Lee W. [7 ]
Ko, Young H. [8 ]
Le, Anne [9 ]
Lea, Michael A. [10 ]
Locasale, Jason W. [3 ,11 ,12 ]
Longo, Valter D. [13 ]
Lyssiotis, Costas A. [14 ,15 ]
McDonnell, Eoin [2 ]
Mehrmohamadi, Mahya
Michelotti, Gregory [1 ]
Muralidhar, Vinayak [16 ,17 ]
Murphy, Michael P. [18 ]
Pedersen, Peter L. [19 ,20 ]
Poore, Brad
Raffaghello, Lizzia [21 ]
Rathmell, Jeffrey C. [2 ,3 ]
Sivanand, Sharanya [22 ]
Vander Heiden, Matthew G. [16 ,17 ,23 ]
Wellen, Kathryn E. [22 ]
机构
[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Duke Mol Physiol Inst, Durham, NC 27701 USA
[3] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[4] Univ Texas SW Med Ctr Dallas, Childrens Med Ctr Res Inst, Dallas, TX 75390 USA
[5] Univ Aberdeen, Rowett Inst Nutr & Hlth, Aberdeen, Scotland
[6] Univ Cambridge, Hutchison MRC Res Ctr, MRC Canc Unit, Cambridge, England
[7] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
[8] Univ Maryland BioPk, KoDiscovery, Baltimore, MD 20201 USA
[9] Johns Hopkins Univ, Sch Med, Sol Goldman Pancreat Canc Res Ctr, Dept Pathol, Baltimore, MD 21231 USA
[10] Rutgers State Univ, New Jersey Med Sch, Newark, NJ 07103 USA
[11] Cornell Univ, Div Nutr Sci, Ithaca, NY 14850 USA
[12] Cornell Univ, Field Genet Gen & Dev, Ithaca, NY 14850 USA
[13] Univ So Calif, Andrus Gerontol Ctr, Div Biogerontol, Los Angeles, CA 90089 USA
[14] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[15] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[16] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[17] Harvard Univ, Sch Med, Harvard MIT Div Hlth Sci & Technol, Boston, MA 02115 USA
[18] Wellcome Trust MRC Bldg, MRC Mitochondrial Biol Unit, Cambridge, England
[19] Johns Hopkins Univ, Dept Biol Chem, Baltimore, MD 21205 USA
[20] Johns Hopkins Univ, Dept Oncol, Baltimore, MD 21205 USA
[21] Ist Giannina Gaslini, Lab Oncol, I-16148 Genoa, Italy
[22] Univ Penn, Dept Canc Biol, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[23] Dana Farber Canc Inst, Boston, MA 02115 USA
基金
英国医学研究理事会;
关键词
Cancer metabolism; Mitochondria; Warburg; Host metabolism; Cancer therapy; PYRUVATE-KINASE M2; N-ACETYLGLUCOSAMINE TRANSFERASE; BREAST-CANCER SURVIVORS; MODIFICATIONS PREDICT PROGNOSIS; GLOBAL HISTONE MODIFICATIONS; SMALL-MOLECULE INHIBITION; HEALTHY FOOD CHOICES; LIFE-SPAN EXTENSION; ATP-CITRATE LYASE; T-CELL MEMORY;
D O I
10.1016/j.semcancer.2015.10.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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. (C) 2015 Elsevier Ltd.
引用
收藏
页码:S129 / S150
页数:22
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