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:Flavones and Aminoflavones Increase the Cytotoxicity of NK Cells in Human Non-Small Cell Lung Cancer.
Flavones and Aminoflavones Increase the Cytotoxicity of NK Cells in Human Non-Small Cell Lung Cancer.
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天然黄酮和合成氨基黄酮具有抗癌特性,但其免疫调节能力尚未得到充分研究。本研究发现,合成黄酮和氨基黄酮可调节自然杀伤(NK)细胞对肺癌细胞的细胞毒作用。值得注意的是,黄酮2、3、6及氨基黄酮8均可提高NK-92MI细胞对A549肺癌细胞的细胞毒性,且不损害正常MRC5细胞。氨基黄酮8增强NK-92MI细胞毒性,表现为IFN-γ、穿孔素和颗粒酶B等细胞毒效应分子表达上升。在共培养条件下,氨基黄酮8还抑制A549肺癌细胞和NK-92MI细胞中的STAT3磷酸化。此外,氨基黄酮8在肺癌异种移植小鼠模型中具有抗肿瘤作用。氨基黄酮8联合NK-92MI细胞治疗产生协同抗肿瘤效应,且未见肝肾毒性。分析显示,氨基黄酮8的C6位氨基对增强NK细胞细胞毒性至关重要。这些发现提示氨基黄酮8可增强NK细胞对肺癌细胞的杀伤,具有作为肺癌新型治疗药物的潜力。
Natural flavonoids (flavones) and synthetic aminoflavones are known for their anti-cancer properties; however, their immunomodulation ability has been largely unexplored.
This study determined that synthetic flavones and aminoflavones modulate the cytotoxicity of natural killer (NK) cells against lung cancer cells.
Notably, flavones 2, 3, and 6 and aminoflavone 8 were shown to increase the cytotoxicity of NK-92MI cells against A549 lung cancer cells without adversely affecting MRC5 normal cells. Aminoflavone 8 enhanced NK-92MI cell cytotoxicity, as evidenced by the elevated expression of cytotoxic effectors, such as IFN- , perforin, and granzyme B. Aminoflavone 8 also inhibited STAT3 phosphorylation in A549 lung cancer and NK-92MI cells under co-culture conditions.
Moreover, aminoflavone 8 exhibited anti-tumour effects in a lung cancer xenograft mouse model. Combined therapy with aminoflavone 8 and NK-92MI cells had synergistic anti-tumour effects without liver or kidney toxicity.
Our analysis revealed that the amino group in the C6 position of aminoflavone 8 was crucial to the enhanced cytotoxicity of NK cells.
These findings suggest that aminoflavone 8 can potentiate NK cell cytotoxicity against lung cancer cells, highlighting its potential as a novel therapeutic agent for the treatment of lung cancer.
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