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.
肿瘤细胞治疗研究
英文原题:miR-150-5p at the Interface of Cancer Biology and Immune Regulation: Dual Roles, Mechanisms, and Therapeutic Opportunities.
miR-150-5p at the Interface of Cancer Biology and Immune Regulation: Dual Roles, Mechanisms, and Therapeutic Opportunities.
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MicroRNAs(miRNAs)是一类小的非编码 RNA,在转录后水平调控基因表达,并在癌症生物学和免疫功能中发挥关键作用。其中,miR-150-5p 已成为一个关键调控因子,在肿瘤发生和免疫细胞分化中具有复杂的、依赖背景的作用。本综述对当前关于 miR-150-5p 的知识进行了全面综合,强调其作为肿瘤抑制因子或癌基因的双重功能取决于癌症类型和细胞背景。
我们审视了其在血液系统恶性肿瘤和实体瘤中的参与,详细阐述了其影响增殖、凋亡和转移的分子机制。特别强调了细胞外囊泡(EV)相关的 miR-150-5p 作为肿瘤微环境(TME)调节因子的作用,包括其对血管生成、免疫逃逸和细胞间通讯的影响。
我们进一步探讨了 miR-150-5p 对关键免疫细胞亚群的调控——如巨噬细胞、树突状细胞、T 细胞和NK 细胞——及其对抗肿瘤免疫的意义。
最后,我们讨论了靶向 miR-150-5p 的治疗潜力和挑战,包括递送障碍、脱靶效应以及个性化医疗的机遇。通过整合近期发现,本综述强调了 miR-150-5p 作为癌症免疫学中生物标志物和治疗靶点的价值。
MicroRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression post-transcriptionally and play crucial roles in cancer biology and immune function. Among them, miR-150-5p has emerged as a key regulator with complex, context-dependent roles in both tumorigenesis and immune cell differentiation. This review provides a comprehensive synthesis of current knowledge on miR-150-5p, highlighting its dual function as a tumor suppressor or oncogene depending on cancer type and cellular context.
We examine its involvement in hematologic malignancies and solid tumors, detailing the molecular mechanisms through which it influences proliferation, apoptosis, and metastasis. Particular emphasis is placed on the role of extracellular vesicle (EV)-associated miR-150-5p as a modulator of the tumor microenvironment (TME), including its impact on angiogenesis, immune evasion, and intercellular communication.
We further explore miR-150-5p's regulation of key immune cell subsets-such as macrophages, dendritic cells, T cells, and natural killer cells-and its implications for anti-tumor immunity.
Finally, we discuss the therapeutic potential and challenges of targeting miR-150-5p, including delivery barriers, off-target effects, and opportunities for personalized medicine. By integrating recent findings, this review underscores miR-150-5p's value as both a biomarker and a therapeutic target in cancer immunology.
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