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.
肿瘤细胞治疗研究
英文原题:Perioperative Changes in Peripheral Natural Killer Cell Activity and Their Association With Clinicopathological Features in Breast Cancer: A Single-Center Cohort Study.
Perioperative Changes in Peripheral Natural Killer Cell Activity and Their Association With Clinicopathological Features in Breast Cancer: A Single-Center Cohort Study.
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手术治疗似乎对乳腺癌患者外周血 NK 细胞活性产生有利影响。NK 活性变化与临床病理参数之间缺乏明确相关性,提示 NK 反应可能反映个体化的免疫能力,而非肿瘤特异性特征。需要整合 NK 细胞亚群和功能表型分析的大型前瞻性研究,以更好地界定 NK 细胞活性在乳腺癌中的预后和预测价值。
本研究旨在评估乳腺癌患者围手术期外周血自然杀伤(NK)细胞活性(ACT)的变化,并探讨NK活性与临床病理特征之间的关系。
对34例有术前和术后NK活性检测数据的女性患者进行了单中心回顾性队列分析。临床和病理变量取自病历记录。比较了两个时间点的NK活性水平,并评估了NK活性差异与年龄、肿瘤大小、TNM分期、激素受体状态、HER2表达、Ki-67指数、转移淋巴结数目及血清肿瘤标志物之间的关联。NK细胞活性采用NK Vue检测法(ATgen,城南,韩国)进行评估,该方法是一种基于干扰素-γ(IFN-)释放的全血刺激检测法。
术后NK活性较术前显著升高(p = 0.041)。然而,NK活性的变化与肿瘤分期、淋巴结受累、肿瘤大小、增殖指数、受体状态、HER2表达、转移淋巴结计数或血清肿瘤标志物均无显著关联(均p > 0.05)。随访期间总体转移率较低。
This study aimed to evaluate perioperative changes in peripheral blood natural killer (NK) cell activity (ACT) in patients with breast cancer and to investigate the relationship between NK activity and clinicopathological characteristics.
A single-center retrospective cohort including 34 female patients with available preoperative and postoperative NK activity measurements was analyzed. Clinical and pathological variables were obtained from medical records. NK activity levels at two time points were compared, and the association between NK activity difference and age, tumor size, TNM stage, hormone receptor status, HER2 expression, Ki-67 index, number of metastatic lymph nodes, and serum tumor markers was assessed. NK cell activity was assessed using the NK Vue assay (ATgen, Seongnam, Republic of Korea), a whole-blood stimulation assay based on interferon-gamma (IFN- ) release.
Postoperative NK activity significantly increased compared with preoperative levels (p = 0.041). However, the change in NK activity was not significantly associated with tumor stage, lymph node involvement, tumor size, proliferation index, receptor status, HER2 expression, metastatic lymph node count, or serum tumor markers (all p > 0.05). The overall metastatic rate during follow-up was low.
Surgical treatment appears to exert a favorable effect on peripheral NK cell activity in breast cancer. The absence of a clear correlation between NK activity changes and clinicopathological parameters suggests that NK responses may reflect an individualized immunologic capacity rather than tumor-specific features. Larger prospective studies integrating NK cell subsets and functional phenotyping are required to better define the prognostic and predictive value of NK cell activity in breast cancer.
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