| Literature DB >> 30551032 |
Nayoung Kim1, Ji-Wan Choi2, Ah Young Song2, Woo Seon Choi2, Hye-Ran Park2, Sojung Park3, Inki Kim4, Hun Sik Kim5.
Abstract
This study identified 8-azaguanine (8-AG) as a novel immunomodulatory drug (IMiD) through a high-throughput screen of the Preswick Chemical Library in a model of human NK cell cytotoxicity against blood cancer cells. 8-AG, originally developed as an antineoplastic agent, significantly increased the cytotoxicity of NK cells and was superior in this activity to previously known IMiDs, such as fluoxetine and amphotericin B, identified from the same library. IFN-γ expression was also slightly increased by 8-AG. Mechanistically, 8-AG increased conjugate formation between NK and target cells and subsequent cytolytic granule polarization, but not calcium mobilization, regulation of activating receptors, or expression of perforin or granzyme B. Thus, the antineoplastic activity of 8-AG should be re-evaluated in light of this novel potentiating effect on NK cells.Entities:
Keywords: 8-azaguanine; Cytotoxicity; Immunomodulatory drugs; Library screening; NK cells
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Year: 2018 PMID: 30551032 DOI: 10.1016/j.intimp.2018.12.020
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932