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:Modification of soluble dietary fiber from quinoa bran and investigation of its anticancer activity in vitro.
Modification of soluble dietary fiber from quinoa bran and investigation of its anticancer activity in vitro.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
SDF-Zn 复合物有潜力用作人肝癌的治疗剂。© 2025 Society of Chemical Industry。
为探究藜麦麸皮可溶性膳食纤维(SDF)的免疫及抗癌作用,本研究采用简便方法制备SDF-锌复合物(SDF-Zn),以增强SDF的生物活性。将SDF-Zn与NK细胞共培养,研究其激活NK细胞的能力。随后,通过细胞增殖、划痕愈合实验、流式细胞术、实时聚合酶链反应和western blot,研究其诱导HepG2人肝癌细胞凋亡的能力。
结果显示,螯合SDF和锌离子显著增强了NK细胞对HeLa细胞的细胞毒性(150 μg mL-1时为48.76%),并显著(P < 0.05)提高了IFN-γ、TNF-α、granzyme-B和NKp44的水平。将SDF-Zn与包括AGS、HeLa、HCT116和HepG2在内的常见人类癌细胞共培养,结果显示SDF-Zn显著(P < 0.05)抑制了HepG2细胞增殖。活性氧的过量产生增加了凋亡基因包括Bax和caspase-3的表达,死亡细胞数量达到45.91%。SDF-Zn对HepG2细胞的抑制作用通过MAPK和NF-κB信号通路发生。
To investigate the immunological and anticancer actions of quinoa bran soluble dietary fiber (SDF), this study used a simple approach to develop an SDF-zinc complex (SDF-Zn) to enhance the biological activity of SDF. SDF-Zn was co-cultured with NK cells to investigate its ability to activate NK cells. Then, its ability to induce apoptosis in HepG2 human hepatoma cells was investigated using cell proliferation, scratch wound healing assay, flow cytometry, real-time polymerase chain reaction and western blot.
The results revealed that chelating SDF and zinc ions considerably increased the cytotoxicity of NK cells against HeLa cells (48.76% at 150 μg mL -1 ) and significantly (P < 0.05) increased the levels of IFN-γ, TNF-α, granzyme-B and NKp44. SDF-Zn was co-cultured with common human cancer cells including AGS, HeLa, HCT116 and HepG2, and the results revealed that SDF-Zn significantly (P < 0.05) inhibited HepG2 cell proliferation. The overproduction of reactive oxygen species increased the expression of apoptotic genes including Bax and caspase-3, and the number of dead cells reached 45.91%. The inhibitory effect of SDF-Zn on HepG2 cells occurred through the MAPK and NF-κB signaling pathways.
Overall, the SDF-Zn complex has the potential to be used as a therapeutic agent for human liver cancer. © 2025 Society of Chemical Industry.
MEMBER ACCOUNT
登录成功会直接打开下一页。