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释放纳米技术以重新定义乳腺癌中肿瘤相关巨噬细胞的动态和非编码 RNA 串扰。

Unleashing nanotechnology to redefine tumor-associated macrophage dynamics and non-coding RNA crosstalk in breast cancer.

机构信息

Biological and Life Sciences, School of Arts and Sciences, Ahmedabad University, Central Campus, Navrangpura, Ahmedabad 380009, Gujarat, India.

出版信息

Nanoscale. 2024 Oct 10;16(39):18274-18294. doi: 10.1039/d4nr02795g.

DOI:10.1039/d4nr02795g
PMID:39292162
Abstract

Breast cancer is a significant global health issue. Tumor-associated macrophages (TAMs) are crucial in influencing the tumor microenvironment and the progression of the disease. TAMs exhibit remarkable plasticity in adopting distinct phenotypes ranging from pro-inflammatory and anti-tumorigenic (M1-like) to immunosuppressive and tumor-promoting (M2-like). This review elucidates the multifaceted roles of TAMs in driving breast tumor growth, angiogenesis, invasion, and metastatic dissemination. Significantly, it highlights the intricate crosstalk between TAMs and non-coding RNAs (ncRNAs), including microRNAs, long noncoding RNAs, and circular RNAs, as a crucial regulatory mechanism modulating TAM polarization and functional dynamics that present potential therapeutic targets. Nanotechnology-based strategies are explored as a promising approach to reprogramming TAMs toward an anti-tumor phenotype. Various nanoparticle delivery systems have shown potential for modulating TAM polarization and inhibiting tumor-promoting effects. Notably, nanoparticles can deliver ncRNA therapeutics to TAMs, offering unique opportunities to modulate their polarization and activity.

摘要

乳腺癌是一个重大的全球健康问题。肿瘤相关巨噬细胞(TAMs)在影响肿瘤微环境和疾病进展方面起着至关重要的作用。TAMs 在表现出不同表型的能力上具有显著的可塑性,从促炎和抗肿瘤(M1 样)到免疫抑制和促进肿瘤(M2 样)。这篇综述阐明了 TAMs 在推动乳腺肿瘤生长、血管生成、侵袭和转移扩散中的多方面作用。值得注意的是,它强调了 TAMs 与非编码 RNA(ncRNA)之间的复杂相互作用,包括 microRNAs、长非编码 RNA 和环状 RNA,作为调节 TAM 极化和功能动态的关键调控机制,为治疗提供了潜在的靶点。基于纳米技术的策略被探索作为一种有前途的方法,用于将 TAMs 重新编程为抗肿瘤表型。各种纳米颗粒递送系统已显示出调节 TAM 极化和抑制促进肿瘤作用的潜力。值得注意的是,纳米颗粒可以将 ncRNA 治疗药物递送到 TAMs 中,为调节其极化和活性提供了独特的机会。

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