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:Value of the combination of intraepithelial tumor-infiltrating lymphocyte density and the heterogeneity of density as a prognostic marker in stage III colorectal cancers.
Value of the combination of intraepithelial tumor-infiltrating lymphocyte density and the heterogeneity of density as a prognostic marker in stage III colorectal cancers.
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TIL(肿瘤浸润淋巴细胞)密度是结直肠癌(CRC)的预后因素和预测因素。TIL密度在肿瘤内的异质性是否对CRC的临床结局起重要作用尚不明确。对接受辅助化疗的III期CRC患者,根据TIL密度和密度异质性分析生存情况,前者通过机器学习方法在CD8免疫染色切片上测定,后者通过计算Simpson均匀度指数确定。在多因素无复发生存分析中,上皮内TIL密度高异质性被发现有独立预后价值,风险比为1.970(1.207-3.215)。高异质性与高T分期、静脉侵犯、神经周围侵犯和KRAS突变密切相关。上皮内TIL密度与密度异质性联合与患者预后显著相关:低TIL密度/高TIL异质性在发现队列和验证队列中的风险比分别为3.284(1.639-6.578)和4.176(1.713-10.178)。我们的研究结果表明,上皮内TIL密度的异质性状态与上皮内TIL密度联合时,可能有助于区分生存较好与较差的患者。
Tumor-infiltrating lymphocyte (TIL) density is both a prognostic and a predictive factor in colorectal cancer (CRC). Whether the heterogeneity of TIL density across the tumor plays an important role in the clinical outcome of CRC is not well known. Adjuvant chemotherapy-treated patients with stage III CRC were analyzed for survival according to TIL density and density heterogeneity, which were determined on CD8-immunostained slides using a machine learning method and by calculating the Simpson evenness index, respectively.
High heterogeneity of the intraepithelial TIL density was found to be an independent prognostic factor, with a hazard ratio of 1. 970 (1. 207-3. 215) in the multivariate analysis of recurrence-free survival. High heterogeneity was closely associated with a high T category, venous invasion, perineural invasion, and KRAS mutation.
The combination of both intraepithelial TIL density and density heterogeneity was significantly associated with the prognosis of patients: low TIL density/high TIL heterogeneity showed hazard ratios of 3. 284 (1. 639-6. 578) and 4. 176 (1. 713-10. 178) in the discovery and validation cohorts, respectively.
Our findings suggest that the heterogeneity status of intraepithelial TIL density might help delineate patients with better vs. worse survival when combined with intraepithelial TIL density.
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