4.6 Review

DNA Damage Response and Metabolic Reprogramming in Health and Disease

Journal

TRENDS IN GENETICS
Volume 36, Issue 10, Pages 777-791

Publisher

CELL PRESS
DOI: 10.1016/j.tig.2020.06.018

Keywords

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Funding

  1. Horizon 2020 ERC Consolidator Grant 'DeFiNER' [GA 64663]
  2. Horizon 2020 Marie Curie ITN [GA 812829, GA 812830, GA 622934]
  3. Sante Foundation
  4. ELIDEK [631]
  5. European Social Fund (ESF) through the Operational Programme 'Human Resources Development, Education and Lifelong Learning 2014-2020' in the context of the project 'Dissecting the functional link between genome instability and RNA metabolism during mammali [MIS 5048456]
  6. Deutsche Forschungsgemeinschaft [SCHU 2494/3-1, SCHU 2494/71, SCHU 2494/10-1, SCHU 2494/11-1, SFB 829, SFB 670, KFO 286, KFO 329, GRK2407]
  7. Deutsche Krebshilfe [70112899]

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Nuclear DNA damage contributes to cellular malfunction and the premature onset of age-related diseases, including cancer. Until recently, the canonical DNA damage response (DDR) was thought to represent a collection of nuclear processes that detect, signal and repair damaged DNA. However, recent evidence suggests that beyond nuclear events, the DDR rewires an intricate network of metabolic circuits, fine-tunes protein synthesis, trafficking, and secretion as well as balances growth with defense strategies in response to genotoxic insults. In this review, we discuss how the active DDR signaling mobilizes extranuclear and systemic responses to promote cellular homeostasis and organismal survival in health and disease.

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