同源重组
卵巢癌
互动者
卵巢癌
癌症研究
生物
癌症
免疫学
细胞生物学
基因
遗传学
作者
Vanessa Klapp,Lorenzo Galluzzi
标识
DOI:10.1016/j.trecan.2021.11.006
摘要
Depending on intensity and duration, STING1 (stimulator of interferon response cGAMP interactor 1) signaling can restrain or promote tumor progression via both cancer cell-intrinsic and -extrinsic pathways. Bruand et al. recently identified a novel STING1-driven immunosuppressive pathway that can be targeted toward superior disease control in preclinical models of homologous recombination deficient (HRD) ovarian carcinoma.
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