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:Role of androgen receptor signaling pathway-related lncRNAs in the prognosis and immune infiltration of breast cancer.
Role of androgen receptor signaling pathway-related lncRNAs in the prognosis and immune infiltration of breast cancer.
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雄激素受体(AR)与乳腺癌(BRCA)密切相关。本研究旨在探讨雄激素受体信号通路相关长链非编码RNA(ARSP相关lncRNA)对乳腺癌(BRCA)亚型分类过程及肿瘤微环境(TME)的影响。
本研究筛选ARSP相关lncRNA以构建风险模型。采用单样本基因集富集分析(ssGSEA)方法检测低危组和高危组患者所产生的免疫反应之间的差异。在聚类分析过程之后,探讨ARSP相关lncRNA与TME之间的关系。采用单因素Cox分析和Lasso回归分析方法筛选出其中9个lncRNA以建立风险模型。观察到风险评分可作为独立预后因素,影响BRCA患者的预后。通过分析生成的校准曲线和列线图评估模型的有效性。
此外,还探讨了风险评分对TME中免疫细胞浸润程度的影响。M2巨噬细胞与风险评分呈正相关,而NK细胞、CD4+ T细胞和初始B细胞与风险评分呈负相关。聚类分析获得的结果表明,免疫评分与聚类亚型相关。
最后,对风险评分和聚类亚型进行分析,以研究患者对不同药物的敏感性,从而确定合适的治疗药物。ARSP相关lncRNA能够准确预测BRCA患者的预后。
Androgen receptor (AR) is strong association with breast cancer (BRCA).
We aimed to investigate the effect of the androgen receptor signaling pathway-related long non-coding RNAs (ARSP-related lncRNAs) on the process of subtype classification and the tumor microenvironment (TME) of breast cancer (BRCA).
Our study screen ARSP-related lncRNAs for the construction of a risk model. The single-sample gene set enrichment analysis (ssGSEA) method was used to detect the differences between the immune responses generated by the patients belonging to the low- and high-risk groups. The relationship between the ARSP-related lncRNAs and TME was explored following the process of cluster analysis.
The univariate Cox analysis and the Lasso regression analysis method was used to screen nine of these lncRNAs to develop a risk model. It was observed that risk score could function as an independent prognostic factor, affecting the prognoses of patients suffering from BRCA. The validity of the model was assessed by analyzing the generated calibration curves and a nomogram.
Additionally, the effect of the risk score on the extent of immune cell infiltration realized in TME was explored. M2 macrophages correlated positively, whereas NK cells, CD4+ T cells, and naive B cells correlated negatively with the risk score. Results obtained using the cluster analysis indicated that immune scores correlated with clustered subtypes.
Finally, the risk score and cluster subtypes were analyzed to study the sensitivity of the patients toward different drugs to identify the appropriate therapeutic agents. The prognoses of patients suffering from BRCA can be accurately predicted by ARSP-related lncRNAs.
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