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:Nanotechnology Meets the Tumor Microenvironment: Unlocking New Horizons in Cancer Therapy.
Nanotechnology Meets the Tumor Microenvironment: Unlocking New Horizons in Cancer Therapy.
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肿瘤微环境(TME)是癌症进展的重要调控者,其形成不仅受基因突变影响,也受酸性pH、细胞外基质(ECM)失调、免疫抑制细胞和细胞因子网络等动态因素影响。这些因素共同促进治疗耐药和转移,给传统治疗带来挑战。纳米技术已成为破除TME屏障的变革性方法,可实现精准靶向和改善药物递送。另一重点是克服ECM致密和免疫抑制。例如,负载透明质酸酶或胶原酶的ECM降解纳米颗粒(NP)可改善药物穿透;免疫调节型NP则可将巨噬细胞从促肿瘤M2表型重编程为抗肿瘤M1表型。与这些策略相辅相成,CAR-T 或自然杀伤(NK)细胞等免疫细胞工程技术可与NP递送的检查点抑制剂协同,增强抗肿瘤免疫。
此外,pH敏感和酶响应型NP可利用TME特异条件实现药物控释,降低全身毒性。尽管临床前结果令人鼓舞,临床转化仍面临障碍,包括优化NP生物相容性、可规模化生产和长期安全性,以及应对患者间TME异质性。
因此,本综述探讨适应TME复杂性的创新NP设计,包括以抗体、叶酸、转铁蛋白、肽和氨基酸进行表面修饰。这些功能化NP可增强肿瘤特异性靶向并逃避免疫清除,从而提高化疗疗效、减少脱靶作用。综述还评估靶向TME的现有NP临床试验进展,并讨论结合实时成像与治疗的新兴诊疗一体化平台。通过整合材料科学、免疫学和系统生物学等多学科见解,纳米技术有望推动个体化癌症治疗。未来研究需优先实现规模化生产,并采用稳健的生物标志物驱动策略,充分实现这一肿瘤学范式转变。
The tumor microenvironment (TME) is a critical orchestrator of cancer progression, shaped not only by genetic mutations but also by dynamic factors such as acidic pH, dysregulated extracellular matrix (ECM), immunosuppressive cells, and cytokine networks. These elements collectively foster therapeutic resistance and metastasis, challenging conventional treatments. Nanotechnology has emerged as a transformative approach to dismantling TME barriers, enabling precise targeting and enhanced drug delivery.
In addition, a key focus is overcoming ECM density and immunosuppression. For instance, ECM-degrading nanoparticles (NPs) loaded with hyaluronidase or collagenase improve drug penetration, while immune-modulating NPs reprogram macrophages from protumor (M2) to antitumor (M1) phenotypes. Complementing these strategies, advances in immune cell engineering, such as chimeric antigen receptor (CAR) T cells or natural killer (NK) cells, are synergized with NPs-delivered checkpoint inhibitors to amplify antitumor immunity.
Additionally, pH-sensitive and enzyme-responsive NPs exploit TME-specific conditions for controlled drug release, minimizing systemic toxicity. Despite promising preclinical results, clinical translation faces hurdles. Challenges include optimizing NPs' biocompatibility, scalability, and long-term safety as well as addressing interpatient TME heterogeneity.
Thus, this review explores innovative NPs designs engineered to navigate the TME complexity, including surface modifications with antibodies, folic acid, transferrin, peptides, and amino acids. These functionalized NPs improve tumor-specific targeting while evading immune clearance, thereby enhancing chemotherapeutic efficacy and reducing off-target effects.
Moreover, this review evaluates current progress in NPs-based clinical trials targeting the TME and discusses emerging theranostic platforms that combine real-time imaging with therapy. By integration of multidisciplinary insights from materials science, immunology, and systems biology, nanotechnology holds immense potential to unlock personalized cancer therapies. Future research must prioritize scalable manufacturing and robust biomarker-driven approaches to realize this paradigm shift in oncology fully.
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