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:Signaling new therapeutic opportunities: cytokines in prostate cancer.
Signaling new therapeutic opportunities: cytokines in prostate cancer.
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基于细胞因子的疗法提供了一种替代性免疫策略,可靶向 T 细胞之外的多效性前列腺癌肿瘤微环境。未来前列腺癌的免疫治疗策略应针对这些免疫细胞群体,它们可能在前列腺癌肿瘤微环境中发挥更重要的作用。
尽管FDA于2010年批准了sipuleucel-T,但在未经选择的prostate cancer患者中使用immune checkpoint inhibitors的努力并未改善临床结局。这些努力包括单独使用anti-PD1/PD-L1和anti-CTLA-4以及将其与现有标准治疗联合的研究。这些策略通常以T细胞为中心,忽视了prostate cancer tumor microenvironment中更广泛的复杂和多效性组成部分,如natural killer cells、myeloid-derived suppressor cells和tumor-associated macrophages。涵盖领域:我们进行了在线文献检索,并对与prostate cancer相关的cytokine-based therapy的现有临床前和临床文献进行了综述,特别是关于interleukin (IL)-2、IL-15、IL-12、IL-23、IL-8和转化生长因子 (TGF)-β。
INTRODUCTION: Despite FDA approval of sipuleucel-T in 2010, endeavors to use immune checkpoint inhibitors in unselected prostate cancer patients have not improved clinical outcomes. These efforts include studies with anti-PD1/PD-L1 and anti-CTLA-4 alone and in combination with existing standards of care. These strategies are generally T-cell centric and disregard the broader complex and pleiotropic components of the prostate cancer tumor microenvironment such as natural killer cells, myeloid-derived suppressor cells, and tumor-associated macrophages.
AREAS COVERED: We performed an online literature search and undertook a review of existing preclinical and clinical literature for cytokine-based therapy related to prostate cancer, specifically on interleukin (IL)-2, IL-15, IL-12, IL-23, IL-8, and transforming growth factor (TGF)-β.
EXPERT OPINION: Cytokine-based therapies present an alternative immune strategy to target the pleiotropic prostate cancer tumor microenvironment beyond T-cells. Future immunotherapy strategies in prostate cancer should address these immune cell populations, which may play more important roles in the prostate cancer tumor microenvironment.
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