TACO1通过Notch1/Hes1信号通路促进胃癌细胞的增殖和迁移,并与免疫细胞浸润有关

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Na Li , Zijie Wei , Xiang Li , Jiayu Jian , Lulu Zhou , Siqi Wang , Miao Chen , Yu Cheng
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引用次数: 0

摘要

细胞色素c氧化酶1翻译激活因子(TACO1)是一种线粒体rna结合蛋白,在线粒体翻译中起重要作用。然而,迄今为止还没有研究评估TACO1在胃癌中的表达、生物学功能和潜在的分子作用机制的变化。因此,我们探讨TACO1在胃癌中的临床意义、生物学功能和免疫系统调节。我们发现TACO1在胃癌中表达上调并与不良预后相关。在机制上,TACO1通过调节Notch1/Hes1信号通路促进胃癌细胞的增殖和迁移。此外,TACO1表达的变化影响多种免疫成分,调节免疫抑制性肿瘤微环境(TME)的产生。总之,我们首次报道了TACO1在胃癌中的作用,研究结果表明TACO1可能是一种有希望的胃癌预后和免疫生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TACO1 facilitates the proliferation and migration of gastric cancer cells via Notch1/Hes1 signaling and is associated with immune cell infiltration
Translational activator of cytochrome c oxidase 1 (TACO1) is a mitochondrial RNA-binding protein playing a fundamental role in mitochondrial translation. However, no studies to date have evaluated changes in the expression, biological functions, and potential molecular mechanisms of action of TACO1 in gastric cancer. Therefore, we investigated the clinical significance, biological function, and immune system modulation associated with TACO1 in gastric cancer. We found that TACO1 expression was upregulated in gastric cancer and associated with poor prognosis. Mechanistically, TACO1 facilitated gastric cancer cell proliferation and migration through modulation of the Notch1/Hes1 signaling pathways. Moreover, the change in TACO1 expression affected multiple immunological components to regulate the generation of an immunosuppressive tumor microenvironment (TME). In conclusion, we first report on the role of TACO1 in gastric cancer, with findings suggesting that TACO1 could represent a promising prognostic and immunological biomarker for gastric cancer.
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来源期刊
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
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