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:Keratin 80 serves as a potential biomarker in metastatic breast cancer.
Keratin 80 serves as a potential biomarker in metastatic breast cancer.
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KRT80 可能与 BC 的转移相关,并可能作为 mBC 治疗的潜在治疗靶点。
乳腺癌(BC)是女性最常见的癌症类型,其发病率和死亡率高得惊人,尤其是转移性乳腺癌(mBC)。
我们的目的是探索mBC的潜在预后生物标志物。BC的RNA-seq数据从癌症基因组图谱和基因表达综合数据库中下载。
通过WGCNA、差异表达基因分析和蛋白质-蛋白质相互作用网络鉴定候选基因。通过Kaplan-Meier和多因素Cox回归分析评估核心基因Keratin 80(KRT80)的预后预测性能。使用qPCR和western blot实验验证KRT80在BC细胞系中的表达。通过体外功能丧失和功能获得实验进一步检测KRT80在BC中的功能作用。
公共数据库的结果表明,与原发性BC组相比,mBC组中KRT80表达显著增加,并且与对照组相比,BC组织中KRT80水平也升高。同时,ROC曲线分析证明了KRT80对mBC的潜在诊断价值。值得注意的是,KRT80水平升高被发现在BC患者中是不良预后的独立预测因素。GSEA分析表明KRT80参与NF-kappa B信号通路。此外,免疫细胞浸润分析的结果显示KRT80表达与CD8 T细胞、活化NK细胞之间存在显著负相关。药物敏感性分析表明,KRT80高表达的患者可能对Lapatinib表现出更高的敏感性。在功能上,KRT80过表达促进了BT549细胞(一种转移性BC细胞系)的活力、迁移、侵袭和上皮-间质转化(EMT)。
Breast cancer (BC) is the most common type of female cancer with alarmingly high morbidity and mortality, especially metastatic BC (mBC).
Our object is to explore a potential prognostic biomarker for mBC. The RNA-seq data of BC were downloaded from The Cancer Genome Atlas and Gene Expression Omnibus databases.
The identification of candidate genes was achieved through the WGCNA, differentially expressed gene analysis and protein-protein interaction network. The prognostic predictive performance of the hub gene, Keratin 80 (KRT80), was evaluated through the Kaplan-Meier and multivariate Cox regression analysis. Validation of the expression of KRT80 in BC cell lines was carried out using qPCR and western blot experiments. The functional role of KRT80 in BC was further examined through loss- and gain-of-function assays in vitro.
The results from the public database indicated a significant increase in KRT80 expression within the mBC group when compared to the primary BC group, and also heightened KRT80 levels were observed in BC tissues relative to the control group. Meanwhile, ROC curve analysis demonstrated the potential diagnostic potential of KRT80 for mBC. Notably, elevated KRT80 levels were found to be an independent predictor of unfavorable prognosis for BC patients. GSEA analysis demonstrated the involvement of KRT80 in NF-kappa B signaling pathway. Furthermore, the results of immune cell infiltration analysis revealed a marked negative correlation between KRT80 expression and CD8 T cells, activated NK cells. Drug sensitivity analysis showed that patients with high expression of KRT80 may exhibit increased sensitivity to Lapatinib. Functionally, overexpression of KRT80 facilitated the viability, migration, invasion and epithelial-mesenchymal transition (EMT) in BT549 cells, a metastatic BC cell line.
Collectively, KRT80 may be linked with metastasis of BC, and it may serve as a potential therapeutic target for mBC treatment.
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