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:Tumor-Infiltrating Immune Cells in Colorectal Cancer.
Tumor-Infiltrating Immune Cells in Colorectal Cancer.
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结直肠癌包含一组异质性恶性肿瘤,其在病理生理机制、免疫反应与浸润、治疗反应以及临床预后方面均存在差异。大量研究强调了肿瘤浸润免疫细胞在不同类型结直肠肿瘤中的临床相关性,但在细胞类型定义和细胞识别策略上各不相同。当涉及多种免疫亚型时,免疫特征的区分尤为困难,但这对于识别肿瘤微环境中新的细胞间机制至关重要。在本综述中,我们汇总了关于肿瘤浸润免疫细胞的人类和非人类研究,并概述了免疫亚型、其病理生理功能及其在结直肠癌中的预后作用。我们讨论了区分免疫特征如何指导免疫治疗靶点和个性化治疗方案的开发。我们分析了覆盖整个免疫谱系的全面人类蛋白质生物标志物图谱,以提高肿瘤研究的可解释性和应用性,并最终增强免疫治疗、推进结直肠癌患者的精准医学。
Colorectal cancer encompasses a heterogeneous group of malignancies that differ in pathophysiological mechanisms, immune response and infiltration, therapeutic response, and clinical prognosis. Numerous studies have highlighted the clinical relevance of tumor-infiltrating immune cells among different types of colorectal tumors yet vary in cell type definitions and cell identification strategies.
The distinction of immune signatures is particularly challenging when several immune subtypes are involved but crucial to identify novel intercellular mechanisms within the tumor microenvironment. In this review, we compile human and non-human studies on tumor-infiltrating immune cells and provide an overview of immune subtypes, their pathophysiological functions, and their prognostic role in colorectal cancer.
We discuss how differentiating immune signatures can guide the development of immunotherapeutic targets and personalized treatment regimens.
We analyzed comprehensive human protein biomarker profiles across the entire immune spectrum to improve interpretability and application of tumor studies and to ultimately enhance immunotherapy and advance precision medicine for colorectal cancer patients.
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