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:The Prognostic Role of Interferon Gamma-inducible Protein 30 in Clear Cell Renal Cell Carcinoma with Immune Infiltrates.
The Prognostic Role of Interferon Gamma-inducible Protein 30 in Clear Cell Renal Cell Carcinoma with Immune Infiltrates.
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IFI30 是 ccRCC 患者的预后生物标志物。靶向 IFI30 可能为癌症治疗提供新策略并改善 ccRCC 患者的预后。
近期研究表明,干扰素γ诱导蛋白30(IFI30)作为一种干扰素γ诱导蛋白,在针对肿瘤生长的免疫反应中具有重要意义。然而,在透明细胞肾细胞癌(ccRCC)中,IFI30表达水平、患者预后与TIL(肿瘤浸润淋巴细胞)之间的关系仍未得到充分阐明。
为了确定IFI30表达、临床数据与ccRCC患者总生存期(OS)之间的潜在联系,我们采用了多个数据库,包括TCGA、基因表达谱交互分析(GEPIA)和UALCAN。此外,利用TIMER、GEPIA和TISIDB数据库对肿瘤浸润免疫细胞(TIIC)与IFI30之间的关联进行了深入分析。采用免疫组织化学(IHC)检测组织微阵列中IFI30和PD-1的表达水平。通过Worldwide Espacenet®检索了关于ccRCC分子分型和药物的专利。
IFI30的表达与样本类型、淋巴结分期、肿瘤分级和癌症分期表现出强相关性。IFI30表达升高与不良的疾病特异性生存期(DSS)和总生存期(OS)结局相关(p <0.01)。此外,IFI30的过表达与免疫调节分子、趋化因子以及调节性T细胞(Tregs)、自然杀伤(NK)CD56细胞、T辅助1(Th1)细胞、细胞毒性T细胞和T辅助细胞的浸润增加密切相关。IHC分析证实IFI30与PD-1表达之间存在强相关性。
Recent research has demonstrated the significance of Interferon Gamma- Inducible Protein 30 (IFI30), an interferon gamma-induced protein, in the immune response to cancerous growths. However, the relationship between IFI30 expression levels, patient prognosis, and tumor-infiltrating lymphocytes in clear cell renal cell carcinoma (ccRCC) remains inadequately defined.
To ascertain the potential link between IFI30 expression, clinical data, and overall survival (OS) in ccRCC patients, we employed diverse databases, which include TCGA, Gene Expression Profiling Interaction Analysis (GEPIA), and UALCAN. Furthermore, an in-depth analysis of the link between tumor-infiltrating immune cells (TIIC) and IFI30 was carried out using the TIMER, GEPIA, and TISIDB databases. Immunohistochemistry (IHC) was utilized to identify the IFI30 and PD-1 expression levels in a tissue microarray. Patents about molecular classification and drugs in ccRCC were reviewed through Worldwide Espacenet®.
The expression of IFI30 demonstrated a strong association with sample type, lymph node stage, tumor grade, and cancer stage. Elevated IFI30 expression was linked to unfavorable Disease- Specific Survival (DSS) and Overall Survival (OS) outcomes (p <0.01). Furthermore, overexpression of IFI30 was strongly linked to immunomodulatory molecules, chemokines, and increased infiltration of regulatory T cells (Tregs), natural killer (NK) CD56 cells, T helper 1 (Th1) cells, cytotoxic T cells, and T helper cells. IHC analysis confirmed a robust correlation between IFI30 and PD-1 expression.
IFI30 is a prognostic biomarker for ccRCC patients. Targeting IFI30 may provide new strategies for cancer therapy and improve the prognosis of ccRCC patients.
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