Nature Structural & Molecular Biology, Год журнала: 2023, Номер 30(6), С. 841 - 852
Опубликована: Март 16, 2023
Язык: Английский
Nature Structural & Molecular Biology, Год журнала: 2023, Номер 30(6), С. 841 - 852
Опубликована: Март 16, 2023
Язык: Английский
Nature reviews. Immunology, Год журнала: 2022, Номер 23(2), С. 90 - 105
Опубликована: Май 30, 2022
Язык: Английский
Процитировано
329Nature Cancer, Год журнала: 2022, Номер 3(12), С. 1452 - 1463
Опубликована: Дек. 12, 2022
Язык: Английский
Процитировано
320Immunity, Год журнала: 2020, Номер 53(1), С. 115 - 126.e5
Опубликована: Июль 1, 2020
Язык: Английский
Процитировано
268Chemical Reviews, Год журнала: 2022, Номер 122(6), С. 5977 - 6039
Опубликована: Фев. 2, 2022
The stimulator of interferon genes (STING) cellular signaling pathway is a promising target for cancer immunotherapy. Activation the intracellular STING protein triggers production multifaceted array immunostimulatory molecules, which, in proper context, can drive dendritic cell maturation, antitumor macrophage polarization, T priming and activation, natural killer vascular reprogramming, and/or death, resulting immune-mediated tumor elimination generation immune memory. Accordingly, there significant amount ongoing preclinical clinical research toward further understanding role surveillance as well development modulators strategy to stimulate immunity. Yet, efficacy agonists limited by many drug delivery pharmacological challenges. Depending on class agonist desired administration route, these may include poor stability, immunocellular toxicity, immune-related adverse events, or lymph node targeting retention, low uptake delivery, complex dependence magnitude kinetics signaling. This review provides concise summary pathway, highlighting recent biological developments, immunological consequences, implications delivery. also offers critical analysis an expanding arsenal chemical strategies that are being employed enhance efficacy, safety, utility lastly draws attention several opportunities therapeutic advancements.
Язык: Английский
Процитировано
222Nature Reviews Nephrology, Год журнала: 2022, Номер 18(9), С. 558 - 572
Опубликована: Июнь 22, 2022
Язык: Английский
Процитировано
180Signal Transduction and Targeted Therapy, Год журнала: 2021, Номер 6(1)
Опубликована: Июнь 2, 2021
Cell death and immune response are at the core of life. In past decades, endoplasmic reticulum (ER) protein STING1 (also known as STING or TMEM173) was found to play a fundamental role in production type I interferons (IFNs) pro-inflammatory cytokines DNA derived from invading microbial pathogens damaged hosts by activating multiple transcription factors. addition this well-known function infection, inflammation, immunity, emerging evidence suggests that STING1-dependent signaling network is implicated health disease regulating autophagic degradation various cell modalities (e.g., apoptosis, necroptosis, pyroptosis, ferroptosis, mitotic death, immunogenic [ICD]). Here, we outline latest advances our understanding mechanisms pathways autophagy which may shed light on new targets for therapeutic interventions.
Язык: Английский
Процитировано
178Signal Transduction and Targeted Therapy, Год журнала: 2021, Номер 6(1)
Опубликована: Апрель 30, 2021
Abstract Sensing invasive cytosolic DNA is an integral component of innate immunity. cGAS was identified in 2013 as the major sensor that binds dsDNA to catalyze synthesis a special asymmetric cyclic-dinucleotide, 2′3′-cGAMP, secondary messenger bind and activate STING for subsequent production type I interferons other immune-modulatory genes. Hyperactivation signaling contributes autoimmune diseases but serves adjuvant anticancer immune therapy. On hand, inactivation causes deficiency sense clear viral bacterial infection creates tumor-prone microenvironment facilitate tumor evasion surveillance. Thus, activation tightly controlled. In this review, we summarize up-to-date multilayers regulatory mechanisms governing activation, including pre- post-translational regulations, cGAS-binding proteins, additional regulators such ions small molecules. We will also reveal pathophysiological function its product cGAMP human diseases. hope provide review recent research advances biology cGAS-targeted therapies
Язык: Английский
Процитировано
155Nature Nanotechnology, Год журнала: 2022, Номер 17(8), С. 891 - 899
Опубликована: Май 30, 2022
Язык: Английский
Процитировано
132Signal Transduction and Targeted Therapy, Год журнала: 2022, Номер 7(1)
Опубликована: Дек. 23, 2022
Since the discovery of Stimulator Interferon Genes (STING) as an important pivot for cytosolic DNA sensation and interferon (IFN) induction, intensive efforts have been endeavored to clarify molecular mechanism its activation, physiological function a ubiquitously expressed protein, explore potential therapeutic target in wide range immune-related diseases. With orthodox ligand 2'3'-cyclic GMP-AMP (2'3'-cGAMP) upstream sensor 2'3'-cGAMP synthase (cGAS) be found, STING acquires central functionality best-studied signaling cascade, namely cGAS-STING-IFN pathway. However, recently updated research through structural research, genetic screening, biochemical assay greatly extends current knowledge biology. A second pocket was discovered transmembrane domain synthetic agonist. On downstream outputs, accumulating studies sketch primordial multifaceted roles beyond cytokine-inducing function, such autophagy, cell death, metabolic modulation, endoplasmic reticulum (ER) stress, RNA virus restriction. Furthermore, with expansion interactome, details trafficking also get clearer. After retrospecting brief history viral interference milestone events since STING, we present vivid panorama biology taking into account information, especially versatile outputs functions IFN induction. We summarize pathogenesis various diseases highlight development small-molecular compounds targeting disease treatment combination latest research. Finally, discuss open questions imperative answer.
Язык: Английский
Процитировано
103Annual Review of Biochemistry, Год журнала: 2022, Номер 91(1), С. 599 - 628
Опубликована: Март 15, 2022
In the decade since discovery of innate immune cyclic GMP-AMP synthase (cGAS)-2'3'-cyclic (cGAMP)-stimulator interferon genes (STING) pathway, its proper activation and dysregulation have been rapidly implicated in many aspects human disease. Understanding biochemical, cellular, regulatory mechanisms this pathway is critical to developing therapeutic strategies that either harness it boost defense or inhibit prevent unwanted inflammation. review, we first discuss how second messenger cGAMP synthesized by cGAS response double-stranded DNA cGAMP's subsequent cell-type-dependent STING signaling cascades with differential physiological consequences. We then review as an immunotransmitter mediates tightly controlled cell-cell communication being exported from producing cells imported into responding via cell-type-specific transporters. Finally, which thecGAS-cGAMP-STING responds different sources mislocalized pathogen defense, cancer, autoimmune diseases.
Язык: Английский
Процитировано
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