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:Interferon-Gamma Secretion Is Significantly Decreased in Stage III Breast Cancer Patients.
Interferon-Gamma Secretion Is Significantly Decreased in Stage III Breast Cancer Patients.
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尽管部分研究提示分子亚型与肿瘤周围浸润自然杀伤(NK)细胞之间可能存在临床关联,但很少有研究评估女性浸润性乳腺癌患者诊断时外周 NK 细胞活性的临床意义。
本研究回顾分析了 2017 年 3 月至 2021 年 7 月接受根治性手术的 396 例女性浸润性乳腺癌患者。通过酶联免疫吸附试验检测 NK 细胞活化后诱导的干扰素-γ(IFN-γ)分泌,以衡量外周 NK 细胞活性,并开展统计分析以确定其与主要临床病理参数的关系。以诱导 IFN-γ 测得的四分位 NK 细胞活性与分期和体重指数(BMI)显著相关;部分炎症血清学指标——中性粒细胞/淋巴细胞比值(N/L)、血小板/中性粒细胞比值(P/N)和血小板/淋巴细胞比值(P/L)——在各区间显示的 NK 活性也存在显著差异。以 IFN-γ 分泌 100 pg/mL 为阈值的二分类分析显示,IFN-γ<100 pg/mL 组 III 期比例显著升高,腋窝淋巴结转移阳性比例也升高;IFN-γ 分泌随 N 分期升高、BMI 增加而下降。以 250 pg/mL 为阈值分析同样显示,低于 250 pg/mL 组 III 期比例升高,腋窝淋巴结阳性似乎相关,BMI≥30 的比例增加。
对于趋势不一致的部分血清学指标,研究进行了 Bonferroni 事后 ANOVA 检验。经 Bonferroni 校正的 IFN-γ 分泌与 TNM 分期亚组分析显示,I、II、IV 期之间未发现显著差异;但 III 期 IFN-γ<100 pg/mL 者显著多于 IFN-γ 为 250 至 <500 pg/mL 或 ≥500 pg/mL 者。根据本研究,III 期与最低 IFN-γ 分泌水平显著相关。与较高水平相比,较低 IFN-γ 分泌似乎与 BMI 增加相关。与按四分位分析相比,当 IFN-γ 分泌低于 100 pg/mL 时,其与腋窝淋巴结阳性、N 分期升高、BMI 增加以及 N/L 和 P/L 增高(均为提示预后不良的因素)的关联更明显。研究者认为,与诊断时其他昂贵的组织 NK 活性检测相比,外周 IFN-γ 分泌检测可能是一种便捷、有用的治疗前风险评估工具,可帮助筛选可能从免疫治疗等后续治疗中获益的可治愈但高危浸润性乳腺癌患者。
Even though some studies have shown possible clinical relationship between molecular subtypes and tumor infiltrating natural killer (NK) cells around tumors, there are few studies showing the clinical relevance of peripheral NK cell activity at diagnosis in female patients with invasive breast cancer. A total of 396 female invasive breast cancer patients who received curative surgical treatment from March 2017 to July 2021 were retrospectively analyzed. NK cell activation-induced interferon-gamma (IFN- ) secretion measured by enzyme-linked immunosorbent assay was used to measure the activity of peripheral NK cells. Statistical analyses were performed to determine clinical relationships with major clinicopathologic parameters. Quadripartite NK cell activity measured by induced interferon-gamma showed significant relevance with staging and body mass index, and some of the inflammatory serological markers, namely N/L (neutrophil/lymphocyte), P/N (platelet/neutrophil), and P/L (platelet/lymphocyte), showed significantly different NK activity in each interval by univariate analysis. A binary subgroup analysis, setting the IFN- secretion cut-off at 100 pg/mL, showed that stage III was significantly increased and axillary lymph node metastasis positivity was increased in the group of IFN- < 100 pg/mL, and IFN- secretion decreased with an increasing N stage, increased BMI (body mass index), and decreased production of IFN- .
Following this, the same binary analysis, but with the IFN- secretion cut-off at 250 pg/mL, also showed that secretion in stage III was increased in those concentrations with <250 pg/mL, axillary lymph node positivity appeared to be correlated, and BMI 30 increased in prevalence. Additional ANOVA post hoc tests (Bonferroni) were performed on some serological markers that tended to be somewhat inconsistent. By subgroup analysis with Bonferroni adjustment between the IFN- secretion and TNM stage, no significant difference in IFN- secretion could be identified at stages I, II, and IV, but at stage III, the IFN- secretion < 100 pg/mL was significantly higher than 250 IFN- secretion < 500 pg/mL or IFN- secretion 500 pg/mL.
According to this study, stage III was significantly associated with the lowest IFN- secretion. Compared to a higher level of IFN- secretion, a lower level of IFN- secretion seemed to be associated with increased body mass index. Unlike when IFN- secretion was analyzed in quartiles, as the IFN- secretion fell below 100 pg/mL, the correlation between axillary lymph node positivity and increased N stage, increased BMI, and increased N/L and P/L, which are suggested poor prognostic factors, became more pronounced.
We think a peripheral IFN- secretion test might be convenient and useful tool for pretreatment risk assessment and selecting probable candidates for further treatment such as immunotherapy in some curable but high-risk invasive breast cancer patients, compared to other costly assaying of tissue NK cell activity at diagnosis.
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