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Pharmacological modulation of nucleic acid sensors - therapeutic potential and persisting obstacles

Journal

NATURE REVIEWS DRUG DISCOVERY
Volume 18, Issue 11, Pages 845-867

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41573-019-0043-2

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Funding

  1. Department of Radiation Oncology at Weill Cornell Medicine (New York, NY, USA)
  2. Radiation Research Foundation (Kansas City, MI, USA)
  3. US Department of Defense, Breast Cancer Research Program [BC180476P1]
  4. Phosplatin (New York, NY, USA)
  5. Lytix (Oslo, Norway)

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Nucleic acid sensors, primarily TLR and RLR family members, as well as cGAS-STING signalling, play a critical role in the preservation of cellular and organismal homeostasis. Accordingly, deregulated nucleic acid sensing contributes to the origin of a diverse range of disorders, including infectious diseases, as well as cardiovascular, autoimmune and neoplastic conditions. Accumulating evidence indicates that normalizing aberrant nucleic acid sensing can mediate robust therapeutic effects. However, targeting nucleic acid sensors with pharmacological agents, such as STING agonists, presents multiple obstacles, including drug-, target-, disease- and host-related issues. Here, we discuss preclinical and clinical data supporting the potential of this therapeutic paradigm and highlight key limitations and possible strategies to overcome them.

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