RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:PTGDS is a potential marker for lung adenocarcinoma identified in a pancancer analysis.
PTGDS is a potential marker for lung adenocarcinoma identified in a pancancer analysis.
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前列腺素D2合酶(PTGDS)是负责合成前列腺素D2的酶。尽管其作用关键,但PTGDS在肿瘤治疗中仍相对研究不足,且缺乏全面的泛癌分析。通过利用多组学数据整合,本研究阐明了PTGDS在多种癌症中的广泛失调及其与患者生存的相关性。此外,PTGDS在多种肿瘤类型中与干细胞评分、微环境评分、微卫星不稳定性(MSI)状态、肿瘤突变负荷(TMB)和甲基化状态显著相关。另外,在大多数癌症中,PTGDS与免疫的相关性明显,单细胞转录组数据表明其主要与NK 细胞和巨噬细胞相关。值得注意的是,实验验证揭示了PTGDS在抑制A549和H1975肺腺癌细胞增殖中的作用,该作用由脂肪酸降解和细胞周期调控介导。总之,PTGDS具有预后潜力,影响泛癌肿瘤免疫,并在肺腺癌(LUAD)中作为肿瘤抑制因子发挥作用。
Prostaglandin D2 synthase (PTGDS) is the enzyme responsible for synthesizing prostaglandin D2. Despite its crucial role, PTGDS remains relatively understudied in tumor therapy, and comprehensive pancancer analyses are lacking. By leveraging multiomics data integration, this study elucidated the widespread dysregulation of PTGDS across various cancers and its correlation with patient survival.
Moreover, PTGDS is significantly associated with stem cell scores, microenvironmental scores, microsatellite instability (MSI) status, tumor mutational burden (TMB), and methylation status in diverse tumor types.
Additionally, immune correlations with PTGDS are evident across most cancers, with single-cell transcriptome data indicating predominant associations with natural killer cells and macrophages.
Notably, experimental validation revealed the role of PTGDS in inhibiting A549 and H1975 lung adenocarcinoma cell proliferation, which was mediated by fatty acid degradation and cell cycle regulation. In summary, PTGDS has prognostic potential, influences pancancer tumor immunity, and acts as a tumor suppressor in lung adenocarcinoma (LUAD).
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