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:Exosomes-based immunotherapy for cancer: Effective components in the naïve and engineered forms.
Exosomes-based immunotherapy for cancer: Effective components in the naïve and engineered forms.
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如今,癌症治疗是研究人员面临的主要挑战之一。肿瘤细胞形成的主要原因是突变,这些突变导致恶性细胞不受控制地增殖并抑制凋亡。肿瘤细胞还通过多种方法创建能够抑制免疫系统细胞反应的微环境,包括产生可溶性因子和细胞间通讯。肿瘤细胞产生的外泌体释放后,也能影响该微环境中其他细胞的功能。多项研究表明,来自不同来源的外泌体,包括肿瘤细胞和免疫细胞,因其特性可用于治疗癌症。由于肿瘤细胞是多种类型肿瘤肽的丰富来源,它们可以诱导抗肿瘤反应。免疫细胞也产生模拟其来源细胞功能的外泌体,例如来自NK细胞和CTL的外泌体在与肿瘤细胞融合后可直接导致其凋亡。
然而,许多研究人员指出,天然外泌体的治疗功能有限,通过操纵和工程化改造它们可以提高其治疗潜力。有多种方法可以修饰外泌体并提高其治疗潜力。
总的来说,这些方法分为两部分,包括改变外泌体的来源细胞以及封装外泌体以携带不同药物。在这篇综述中,我们将讨论关于天然外泌体和工程化外泌体治疗应用的研究,并提供该领域新研究的最新进展。
Today, cancer treatment is one of the main challenges for researchers. The main cause of tumor cell formation is mutations that lead to uncontrolled proliferation and inhibition of apoptosis in malignant cells. Tumor cells also create a microenvironment that can suppress the immune system cells' responses through various methods, including producing soluble factors and cell-to-cell communication. After being produced from tumor cells, exosomes can also affect the functions of other cells in this microenvironment.
Various studies have shown that exosomes from different sources, including tumor cells and immune cells, can be used to treat cancers due to their characteristics. Since tumor cells are rich sources of various types of tumor peptides, they can induce anti-tumor responses. Immune cells also produce exosomes that mimic the functions of their cells of origin, such that exosomes derived from NK cells and CTLs can directly lead to their apoptosis after merging with tumor cells.
However, many researchers have pointed out that naïve exosomes have a limited therapeutic function, and their therapeutic potential can be increased by manipulating and engineering them. There are various methods to modify exosomes and improve their therapeutic potential.
In general, these methods are divided into two parts, which include changing the cell of origin of the exosome and encapsulating the exosome to carry different drugs. In this review, we will discuss the studies on the therapeutic use of naive and engineered exosomes and provide an update on new studies in this field.
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