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.
肿瘤细胞治疗研究
英文原题:Considerations for selecting immunodeficient mouse strains for cancer xenograft models.
Considerations for selecting immunodeficient mouse strains for cancer xenograft models.
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用于疗效和毒性研究的临床前(体内)实验主要在小鼠中进行。然而,人源细胞、组织和类器官通常会被小鼠的免疫系统排斥。因此,在癌症研究中,免疫缺陷小鼠被用作异种移植模型以克服免疫排斥。异种移植小鼠模型根据移植部位分为异位、原位和转移模型。异种移植小鼠模型通过移植来源于患者的癌细胞、组织或类器官来建立。这些模型因移植材料和受体小鼠的不同而表现出不同的成功率和生产时间。在本综述中,介绍了用于在癌症研究中建立异种移植模型的小鼠品系。免疫细胞(如 T 细胞、B 细胞和NK 细胞)的基因工程显示出特定的特性。为选择免疫缺陷小鼠品系,必须了解这些模型特征的差异。优化的小鼠模型可为研究癌症进展和评估抗癌药物提供信息。
Preclinical (in vivo) experiments for efficacy and toxicity are predominantly conducted in mice. Nevertheless, human-derived cells, tissues, and organoids are generally rejected by the immune system of mice.
Thus, immunodeficient mice are used as xenograft models to overcome immune rejection in cancer research. Xenograft mouse models are divided into ectopic, orthotopic, and metastatic models based on the transplant sites. Xenograft mouse models are established by transplanting cancer cells, tissues, or organoids derived from patients. These models show diverse success rates and production times depending on the transplant materials and recipient mice.
In this review, mouse strains for the establishment of xenograft models in cancer research are introduced. Genetic engineering of immune cells, such as T cells, B cells, and natural killer cells, shows specific properties. To select an immunodeficient mouse strain, the differences in the characteristics of the models must be understood. Optimized mouse models can provide information to investigate cancer progression and evaluate anticancer drugs.
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