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:Immunomodulatory Roles of IL-15 in Immune Cells and its Potential for Cancer Immunotherapy.
Immunomodulatory Roles of IL-15 in Immune Cells and its Potential for Cancer Immunotherapy.
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白细胞介素-15(IL-15)于1994年被发现,是一种T细胞生长因子,能够模拟IL-2的功能。IL-15与抗原提呈细胞(APC)表面表达的IL-15Rα亚基结合,并通过反式提呈机制激活自然杀伤(NK)细胞和CD8+ T细胞表面的IL-2/IL-15Rβγ复合物受体。这种相互作用启动了一系列下游信号通路,在NK细胞、CD8+ T细胞和B细胞的活化、增殖和抗凋亡过程中发挥关键作用。它为肿瘤免疫治疗提供了坚实的理论基础和潜在的治疗靶点。无论是通过主动还是被动免疫治疗策略,IL-15已成为刺激抗肿瘤细胞增殖的关键分子。
Interleukin-15 (IL-15) was identified in 1994 as a T-cell growth factor with the capability to mimic the functions of IL-2. IL-15 engages with the IL-15Rα subunit expressed on the surface of antigen-presenting cells (APCs) and, through a trans-presentation mechanism, activates the IL-2/IL-15Rβγ complex receptor on the surface of natural killer (NK) cells and CD8+ T cells.
This interaction initiates a cascade of downstream signaling pathways, playing a pivotal role in the activation, proliferation, and anti-apoptotic processes in NK cells, CD8+ T cells, and B cells. It provides a substantial theoretical foundation and potential therapeutic targets for tumor immunotherapy. Whether through active or passive immunotherapeutic strategies, IL-15 has emerged as a critical molecule for stimulating anti-tumor cell proliferation.
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