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:BTN3A: A Promising Immune Checkpoint for Cancer Prognosis and Treatment.
BTN3A: A Promising Immune Checkpoint for Cancer Prognosis and Treatment.
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Butyrophilin-3A (BTN3A) 亚家族成员是一组存在于不同细胞类型表面的免疫球蛋白,包括先天免疫细胞和癌细胞。由于它们与 B7 家族成员高度相似,已有不同研究开展并揭示了 BTN3A 分子参与调节肿瘤微环境 (TME) 中 T 细胞活性。然而,这些研究的很大一部分集中在 γδ T 细胞以及 BTN3A 如何促进其功能上。在这篇综述中,我们将描述 BTN3A 分子在不同肿瘤微环境中的作用和各个方面,并回顾 BTN3A 受体如何调节多种免疫效应功能,包括 CD4+ (Th1)、细胞毒性 CD8+ T 细胞和 NK 细胞的功能。我们还将强调 BTN3A 分子作为有效免疫治疗和成功控制癌症的治疗靶点的潜力,这可能代表患者治疗的光明未来。
Butyrophilin-3A (BTN3A) subfamily members are a group of immunoglobulins present on the surface of different cell types, including innate and cancer cells. Due to their high similarity with the B7 family members, different studies have been conducted and revealed the involvement of BTN3A molecules in modulating T cell activity within the tumor microenvironment (TME).
However, a great part of this research focused on γδ T cells and how BTN3A contributes to their functions. In this review, we will depict the roles and various aspects of BTN3A molecules in distinct tumor microenvironments and review how BTN3A receptors modulate diverse immune effector functions including those of CD4+ (Th1), cytotoxic CD8+ T cells, and NK cells.
We will also highlight the potential of BTN3A molecules as therapeutic targets for effective immunotherapy and successful cancer control, which could represent a bright future for patient treatment.
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