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:Some Glycoproteins Expressed on the Surface of Immune Cells and Cytokine Plasma Levels Can Be Used as Potential Biomarkers in Patients with Colorectal Cancer.
Some Glycoproteins Expressed on the Surface of Immune Cells and Cytokine Plasma Levels Can Be Used as Potential Biomarkers in Patients with Colorectal Cancer.
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结直肠癌(CRC)是全球范围内导致死亡的主要原因之一。其发病率在最常见的危及生命的疾病中占据主要位置。因此,基于合适的生物标志物对疾病活动进行早期识别和精确表征,对于治疗策略和患者生存至关重要。识别结直肠癌的新生物标志物或疾病特异性水平的生物标志物/生物标志物组合,将显著有助于患者的精确诊断和改善的个体化治疗。
因此,本研究旨在识别结直肠癌特异性免疫学生物标志物。通过ELISA测定了20例结直肠癌患者和21名健康个体的几种细胞因子(白细胞介素-1β /IL-1β/、IL-2、IL-4、IL-10、IL-12、IL-15、TGFβ和IFNγ)的血浆水平。通过流式细胞术评估了从CRC患者和健康志愿者分离的外周血白细胞表面几种类型糖蛋白的表达。分析了细胞因子水平与细胞表面糖蛋白表达之间的相关性。所获得的结果表明,癌症患者组中表达CD80、CD86、CD279和CD274的白细胞群体水平显著升高,而NK细胞以及CD8和CD25阳性细胞的数量减少。基于这些数据以及与细胞因子水平的相关性,可以得出结论:CD25、CD80、CD86、CD274和CD279糖蛋白联合IL-1β、IL-2、IL-15和TGFβ的特定血浆水平可能代表结直肠癌的潜在生物标志物。
Colorectal cancer (CRC) is a leading cause of mortality worldwide. Its incidence holds a major position among the most common life-threatening diseases. Hence, the early identification and precise characterization of disease activity based on proper biomarkers are of utmost importance for therapeutic strategy and patient survival. The identification of new biomarkers for colorectal cancer or disease-specific levels/combinations of biomarkers will significantly contribute to precise diagnosis and improved personalized treatment of patients.
Therefore, the present study aims to identify colorectal cancer-specific immunological biomarkers. The plasma levels of several cytokines (interleukin-1β /IL-1β/, IL-2, IL-4, IL-10, IL-12, IL-15, TGFβ and IFNγ) of 20 patients with colorectal cancer and 21 healthy individuals were determined by ELISA. The expression of several types of glycoproteins on the surface of peripheral blood leukocytes isolated from CRC patients and healthy volunteers was evaluated by flow cytometry. Correlations between cytokine levels and cell surface glycoprotein expression were analyzed.
The obtained results demonstrated significantly elevated levels of CD80, CD86, CD279 and CD274 expressing leukocyte populations in the cancer patient group, while the numbers of NK cells and CD8- and CD25-positive cells were decreased. Based on these data and the correlations with cytokine levels, it can be concluded that CD25, CD80, CD86, CD274 and CD279 glycoproteins combined with specific plasma levels of IL-1β, IL-2, IL-15 and TGFβ could represent potential biomarkers for colorectal cancer.
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