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:High expression of GRB2 associated binding protein 3 mRNA predicts positive prognosis in melanoma.
High expression of GRB2 associated binding protein 3 mRNA predicts positive prognosis in melanoma.
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恶性黑色素瘤是侵袭性最强的皮肤癌,其特征是转移性疾病患者预后不良。准确预测预后对于治疗决策至关重要。本研究采用生物信息学分析探讨生长因子受体结合蛋白2相关结合蛋白3(GAB3)mRNA的预后价值。分析来自癌症基因组图谱和基因型-组织表达(GTEx)的RNA转录组测序数据和临床数据,以研究黑色素瘤中GAB3 mRNA高表达组和低表达组的差异表达基因。进行基因富集分析并构建蛋白质-蛋白质相互作用网络。GAB3高表达与较低的T分期、黑色素瘤Clark分级、Breslow深度和黑色素瘤溃疡显著相关。GAB3高表达还与T1和T2期及N0期更好的无进展间隔相关,并在T1和T2期、N0期和N1期中与更长的总生存期相关。GAB3促进黑色素瘤中巨噬细胞和活化NK 细胞的高水平浸润。GAB3高表达预测早期黑色素瘤的积极预后,这可能由抗癌免疫反应介导。
Malignant melanoma is the most aggressive form of skin cancer, and it is characterized by poor prognosis in patients with metastatic diseases. Accurate prediction of prognosis is crucial for therapeutic decisions. In this study, bioinformatics analysis was used to explore the prognostic value of growth factor receptor-bound protein 2-associated binding protein 3 (GAB3) mRNA. RNA transcriptome sequencing data and clinical data from The Cancer Genome Atlas and genotype-tissue expression (GTEx) were analyzed for differentially expressed genes in high and low GAB3 mRNA expression groups in melanoma.
Performing gene enrichment analysis and constructing protein-protein interaction networks. High expression of GAB3 was significantly correlated with a lower T stage, melanoma Clark level, Breslow depth, and melanoma ulceration. And high GAB3 expression was also associated with better progression-free interval in T1 and T2 stages and N0 stage and longer overall survival in T1 and T2 stages, N0 stage, and N1 stage.
GAB3 promoted high levels of infiltration of macrophages and activated natural killer cells in melanoma. High expression of GAB3 predicted a positive prognosis in early-stage melanoma that may be mediated by the anticancer immune response.
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