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:Eudragit S100 prepared pH-responsive liposomes-loaded betulinic acid against colorectal cancer in vitro and in vivo.
Eudragit S100 prepared pH-responsive liposomes-loaded betulinic acid against colorectal cancer in vitro and in vivo.
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本研究旨在开发聚合物Eudragit S100用于制备pH响应型负载白桦脂酸的脂质体(pH-BA-LP),以提高结直肠癌化疗的治疗指数。通过薄膜分散法和易于放大的pH驱动法,将负载BA的脂质体包覆Eudragit S100。对制备的脂质体进行了粒径、表面形态、包封率、稳定性、体外药物释放和抗肿瘤活性评价。特别是,pH-BA-LP表现出粒径较小(<100 nm)、包封率为90%、稳定性高以及稳定累积释放等优势。通过检测pH-BA-LP的体内抗肿瘤效果,结果显示其显著抑制了结直肠癌中的肿瘤增殖和细胞迁移。pH-BA-LP还通过调控Akt/TLR介导的信号通路抑制肿瘤生长,并显著下调NFAT1和NFAT4蛋白的表达。
研究发现,pH-BA-LP可增加肿瘤组织中的NK细胞和CD3+细胞,CD3+细胞中CD8+细胞的比例也升高,证明pH-BA-LP可通过增强荷瘤小鼠的自身免疫水平发挥抗肿瘤作用。使用pH-BA-LP后,CD8和CD68的阳性浸润率升高,CD163相对降低,证明pH-BA-LP可调节荷瘤小鼠的免疫浸润水平。
因此,本研究提供了一种有效方法,用于制备pH响应型聚合物包覆脂质体,以实现具有生物活性化合物的结肠递送。
This study aimed to develop polymer Eudragit S100 for preparing pH-responsive liposomes-loaded betulinic acid (pH-BA-LP) to improve the therapeutic index of chemotherapy for colorectal cancer. BA-loaded liposomes were coated with Eudragit S100 by a thin film dispersion and easily scalable pH-driven method. The prepared liposomes were evaluated for size, surface morphology, entrapment efficiency, stability, in vitro drug release, and antitumor activity. In particular, pH-BA-LP showed advantages such as lower size (<100 nm), encapsulation efficiency of 90%, high stability, and stably cumulative release. By detecting the antitumor effects of pH-BA-LP in vivo , it showed that the tumor proliferation and cell migration were significantly inhibited in colorectal cancer.
The pH-BA-LP also inhibited tumor growth via the regulation of Akt/TLR-mediated signalling and significantly down-regulated the expression of NFAT1 and NFAT4 proteins. It was found that pH-BA-LP can increase NK cells and CD3 + cells in tumor tissues, and the proportion of CD8 + cells in CD3 + cells was also increased, which proved that pH-BA-LP can play an antitumor effect by enhancing the autoimmunity level in tumor-bearing mice.
The positive infiltration rates of CD8 and CD68 were increased and CD163 was relatively decreased by using pH-BA-LP, which proved that pH-BA-LP can regulate the immune infiltration levels in tumor-bearing mice.
Therefore, the present work provides an effective method to prepare pH-responsive polymer-coated liposomes for colonic delivery with biologically active compounds.
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