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:Effects of Leea indica leaf extracts and its phytoconstituents on natural killer cell-mediated cytotoxicity in human ovarian cancer.
Effects of Leea indica leaf extracts and its phytoconstituents on natural killer cell-mediated cytotoxicity in human ovarian cancer.
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我们首次证实 L. 的叶提取物。
药用植物丰富的生物多样性及其作为新型疗法和先导化合物来源的重要性,值得进一步研究。尽管减瘤手术和化疗取得进展,卵巢癌复发及治疗耐药风险仍较高,临床结局仍较差,甚至无法治愈。
本研究旨在调查药用植物 Leea indica 叶提取物及其部分植物化学成分对人卵巢癌细胞的作用,以及与 oxaliplatin 和自然杀伤(NK)细胞联用的效果。
采集新鲜健康的 L. indica 叶片,用 70% 甲醇浸渍提取,再以正己烷、二氯甲烷和乙酸乙酯分配粗提物。评估所选提取物和化合物对人卵巢癌细胞活力、NK 细胞细胞毒性及 NK 细胞受体应激配体表达的影响。还使用酶联免疫吸附试验检测其对脂多糖刺激的人 U937 巨噬细胞 TNF-α 和 IL-1 生成的影响。
L. indica 叶提取物提高了人卵巢肿瘤细胞对 NK 细胞介导细胞毒作用的敏感性。methyl gallate 而非 gallic acid 可上调癌细胞应激配体表达。以 methyl gallate 和低浓度 oxaliplatin 联合预处理肿瘤细胞,可增加应激配体表达,并相应增强肿瘤细胞对 NK 细胞介导细胞溶解的敏感性。此外,NK 细胞完全抑制了 methyl gallate 预处理卵巢癌细胞的生长。叶提取物抑制了人 U937 巨噬细胞 TNF-α 和 IL-1 生成;methyl gallate 下调这些细胞因子的效力强于 gallic acid。
我们首次证明,L. indica 叶提取物及其植物化学成分 methyl gallate 可增强卵巢肿瘤细胞对 NK 细胞细胞溶解作用的敏感性。这些结果提示,应进一步研究 methyl gallate、oxaliplatin 和 NK 细胞对卵巢癌细胞的联合效应,例如用于难治性卵巢癌。本研究有助于增进对 L. indica 传统抗癌用途的科学认识。
The rich biodiversity of medicinal plants and their importance as sources of novel therapeutics and lead compounds warrant further research. Despite advances in debulking surgery and chemotherapy, the risks of recurrence of ovarian cancer and resistance to therapy are significant and the clinical outcomes of ovarian cancer remain poor or even incurable.
This study aims to investigate the effects of leaf extracts from a medicinal plant Leea indica and its selected phytoconstituents on human ovarian cancer cells and in combination with oxaliplatin and natural killer (NK) cells.
Fresh, healthy leaves of L. indica were harvested and extracted in 70% methanol by maceration. The crude extract was partitioned with n-hexane, dichloromethane and ethyl acetate. Selected extracts and compounds were analyzed for their effects on cell viability of human ovarian cancer cells, NK cell cytotoxicity, and stress ligands expression for NK cell receptors. They were also evaluated for their effects on TNF- and IL-1 production by enzyme-linked immunosorbent assay in lipopolysaccharide-stimulated human U937 macrophages.
Leaf extracts of L. indica increased the susceptibility of human ovarian tumor cells to NK cell-mediated cytotoxicity. Treatment of cancer cells with methyl gallate but not gallic acid upregulated the expression of stress ligands. Tumor cells pretreated with combination of methyl gallate and low concentration of oxaliplatin displayed increased levels of stress ligands expression and concomitantly enhanced susceptibility to NK cell-mediated cytolysis. Further, NK cells completely abrogated the growth of methyl gallate-pretreated ovarian cancer cells. The leaf extracts suppressed TNF- and IL-1 production in human U937 macrophages. Methyl gallate was more potent than gallic acid in down-regulating these cytokine levels.
We demonstrated for the first time that leaf extracts of L. indica and its phytoconstituent methyl gallate enhanced the susceptibility of ovarian tumor cells to NK cell cytolysis. These results suggest that the combined effect of methyl gallate, oxaliplatin and NK cells in ovarian cancer cells warrants further investigation, for example for refractory ovarian cancer. Our work is a step towards better scientific understanding of the traditional anticancer use of L. indica.
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