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:Nanomedicines Reshape the Tumor Microenvironment: Multidimensional Strategies from Modulating "Barriers" to Metabolic Intervention.
Nanomedicines Reshape the Tumor Microenvironment: Multidimensional Strategies from Modulating "Barriers" to Metabolic Intervention.
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纳米颗粒驱动的肿瘤微环境(TME)重塑代表了一种变革性的癌症治疗策略,从传统方法转向多维调控。本综述探讨了工程化纳米颗粒如何精确靶向并改变TME的关键组分——包括免疫细胞(如NK细胞、树突状细胞、T细胞)、癌相关成纤维细胞和细胞外基质——以克服“化学屏障”和“物理屏障”。此外,我们强调了纳米颗粒在重编程TME代谢中的关键作用,如缓解缺氧、破坏Warburg效应以及调节脂质和腺苷代谢。通过将免疫激活与代谢干预相结合,纳米药物不仅增强抗肿瘤免疫,还恢复代谢平衡,为克服治疗耐药和抑制肿瘤进展提供了一种协同且有效的治疗途径。
Nanoparticle-driven remodeling of the Tumor Microenvironment (TME) represents a transformative strategy in cancer therapy, shifting from traditional approaches to multidimensional modulation. This review explores how engineered nanoparticles precisely target and alter key TME components-including immune cells (eg, NK cells, dendritic cells, T cells), cancer-associated fibroblasts, and the extracellular matrix-to overcome "Chemical barriers" and "physical barriers".
Furthermore, we highlight the pivotal role of nanoparticles in reprogramming TME metabolism, such as alleviating hypoxia, disrupting the Warburg effect, and modulating lipid and adenosine metabolism. By integrating immune activation with metabolic intervention, nanomedicines not only enhance anti-tumor immunity but also restore metabolic balance, offering a synergistic and potent therapeutic avenue for overcoming treatment resistance and inhibiting tumor progression.
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