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 clinical implications and molecular features of intrahepatic cholangiocarcinoma with perineural invasion.
The clinical implications and molecular features of intrahepatic cholangiocarcinoma with perineural invasion.
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我们的研究解析了合并 PNI 的 ICC 的基因组特征以及免疫抑制性易转移生态位。
神经周围侵犯(PNI)与包括肝内胆管癌(ICC)在内的恶性肿瘤转移相关,并提示预后不良。
研究纳入三个大型队列:本团队的ZS-ICC队列和组织芯片(TMA)队列、来自公开数据库的MSK队列,以及一个规模较小的第4队列。在MSK和TMA队列中评估PNI的预后意义;在MSK和ZS-ICC队列中分析PNI相关基因组及转录组特征,并开展GO、KEGG和ssGSEA分析。研究还通过免疫组化分析PNI与神经元、水解酶及免疫细胞标志物的关系,并评估辅助治疗对伴PNI的ICC患者的疗效。
MSK和TMA队列中分别有30.6%和20.7%的ICC患者存在PNI。PNI患者更常见恶性表型,包括CA19-9升高、大胆管型、淋巴结侵犯,以及总生存期(OS)和无复发生存期(RFS)缩短。发生PNI的神经表达交感神经标志物酪氨酸羟化酶(TH)。PNI患者KRAS突变频率较高,并呈现免疫抑制、易转移的微环境,表现为NK细胞减少、中性粒细胞增加,以及PD-L1、CD80和CD86表达升高。接受TEGIO、GEMOX或卡培他滨辅助治疗后,PNI患者的OS延长。
本研究阐明了伴PNI的ICC的基因组特征及其免疫抑制、易转移微环境。PNI患者术后预后较差,但对辅助化疗应答良好。
Perineural invasion (PNI) is associated with metastasis in malignancies, including intrahepatic cholangiocarcinoma (ICC), and is correlated with poor prognosis.
The study included three large cohorts: ZS-ICC and TMA cohorts from our team, MSK cohort from a public database, and a small cohort named cohort 4. Prognostic implications of PNI were investigated in MSK cohort and TMA cohort. PNI-related genomic and transcriptomic profiles were analyzed in MSK and ZS-ICC cohorts. GO, KEGG, and ssGSEA analyses were performed. Immunohistochemistry was used to investigate the relationship between PNI and markers of neurons, hydrolases, and immune cells. The efficacy of adjuvant therapy in ICC patients with PNI was also assessed.
A total of 30.6% and 20.7% ICC patients had PNI in MSK and TMA cohorts respectively. Patients with PNI presented with malignant phenotypes such as high CA19-9, the large bile duct type, lymph node invasion, and shortened overall survival (OS) and relapse-free survival (RFS). Nerves involved in PNI positively express tyrosine hydroxylase (TH), a marker of sympathetic nerves. Patients with PNI showed high mutation frequency of KRAS and an immune suppressive metastasis prone niche of decreased NK cell, increased neutrophil, and elevated PD-L1, CD80, and CD86 expression. Patients with PNI had an extended OS after adjuvant therapy with TEGIO, GEMOX, or capecitabine.
Our study deciphered the genomic features and the immune suppressive metastasis-prone niche in ICC with PNI. Patients with PNI showed a poor prognosis after surgery but a good response to adjuvant chemotherapy.
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