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:Correlation between schistosomiasis and CD8+ T cell and stromal PD-L1 as well as the different prognostic role of CD8+ T cell and PD-L1 in schistosomal-associated colorectal cancer and non-schistosomal-associated colorectal cancer.
Correlation between schistosomiasis and CD8+ T cell and stromal PD-L1 as well as the different prognostic role of CD8+ T cell and PD-L1 in schistosomal-associated colorectal cancer and non-schistosomal-associated colorectal cancer.
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研究表明,CD8+ TILs 是 CRC 和 SCRC 患者 OS 的独立预测因素。PD-L1 的表达与 CD8+ TILs 密度呈正相关。血吸虫病与 CD8+ TILs 及 PD-L1 之间无相关性。间质 PD-L1 而非 tPD-L1 与 OS 显著相关,但它并非独立预后因素。
血吸虫病对CD8+ T细胞的影响以及进而对PD-L1表达的影响尚不清楚,CD8+ TILs作为血吸虫相关性结直肠癌(SCRC)生物标志物的效用鲜有报道。
共纳入338例结直肠癌(CRC)患者。采用免疫组化分析评估PD-L1的表达及CD8+ T细胞浸润情况。
在总队列中,结果显示CD8 + TIL密度与肿瘤内(p = 0.0001)和间质PD-L1表达(p = 0.0102)呈正相关。但血吸虫病与CD8+ TILs和PD-L1之间无相关性。此外,CD8 + TIL密度(p = 0.010)、血吸虫病(p = 0.042)是总生存期(OS)的独立预测因素。间质PD-L1(sPD-L1)与OS相关(p = 0.046),但并非独立预测因素。在无血吸虫病患者中,CD8 + T细胞(p = 0.002)和sPD-L1(p = 0.005)与更好的OS相关。在有血吸虫病患者中,CD8 + T细胞是独立预后因素(p = 0.045)。
The effect of schistosomiasis on CD8+ T cells and then on PD-L1 expression was unknown, and the utility of CD8+ TILs as a biomarker for schistosomal-associated colorectal cancer (SCRC) rarely has been reported.
Three hundred thirty-eight patients with colorectal cancer (CRC) were enrolled. Immunohistochemical analysis was conducted to evaluate the expression of PD-L1 and the infiltration of CD8+ T cells.
In the total cohort, the results showed that CD8 + TIL density was positively correlated with tumoral (p = 0.0001) and stromal PD-L1 expression (p = 0.0102). But there were no correlation between schistosomiasis and CD8+ TILs and PD-L1. Furthermore, CD8 + TIL density (p = 0.010), schistosomiasis (p = 0.042) were independent predictive factors for overall survival (OS). Stromal PD-L1 (sPD-L1) was correlated with OS (p = 0.046), but it was not an independent predictor. In patients without schistosomiasis, CD8 + T cells (p = 0.002) and sPD-L1 (p = 0.005) were associated with better OS. In patients with schistosomiasis, CD8 + T cells were independent prognosis factor (p = 0.045).
The study showed that CD8+ TILs was an independent predictive factor for OS in CRC and SCRC patients. The expression of PD-L1 was positively associated with CD8 + TILs density. There were no correlation between schistosomiasis and CD8 + TILs and PD-L1. Stromal PD-L1 but not tPD-L1 was significantly associated with OS, whereas it was not an independent prognostic factor.
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