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:Comprehensive analysis of targetable mutations and tumor microenvironment in urachal cancer.
Comprehensive analysis of targetable mutations and tumor microenvironment in urachal cancer.
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脐尿管癌是一种罕见的恶性肿瘤,通常在临床就诊时已处于晚期。在这种情况下,一般采用全身化疗进行治疗。然而,关于免疫检查点抑制剂或靶向治疗对脐尿管癌有效性的数据仍然匮乏。我们分析了脐尿管癌的基因组图谱,以识别潜在的可靶向突变并评估肿瘤微环境。回顾性分析了42份脐尿管样本。我们的结果显示,TP53、GNAS和KRAS突变在脐尿管癌中较为常见,且在无MAPK改变的脐尿管癌队列中TP53突变 prevalence 增加。肿瘤微环境显示,在MAPK改变的脐尿管癌中NK细胞增多。最后,我们表明,与膀胱癌相比,脐尿管癌在基因组和转录组上与结直肠癌具有相似性。本研究为脐尿管肿瘤样本的分子图谱提供了新的见解,并提示其与结直肠癌可能存在关联,这可能指导未来的临床试验设计。
Urachal cancer, a rare malignancy, generally presents in the clinical setting with advanced stages of disease. Systemic treatment with chemotherapy is generally utilized in this setting.
However, there remains a paucity of data on the effectiveness of immune checkpoint inhibitors or targeted therapies for urachal cancer.
We analyzed the genomic profile of urachal cancer in order to identify potentially targetable mutations and evaluate the tumor microenvironment. 42 urachal samples were retrospectively analyzed.
Our results showed that TP53, GNAS and KRAS mutations were common in urachal cancer with increased prevalence of TP53 mutation in urachal cohorts without MAPK-alterations. The tumor microenvironment demonstrated increased NK cells in MAPK-altered urachal cancer.
Finally, we show that urachal cancer shares genomic and transcriptomic similarity with colorectal cancer compared to bladder cancer.
This study provides new insights into the molecular profiles of urachal tumor samples and possibility of association with colorectal cancer that might guide future clinical trial design.
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