Jóźwicka Teresa Maria, Erdmańska Patrycja Maria, Stachowicz-Karpińska Agnieszka, Olkiewicz Magdalena, Jóźwicki Wojciech
Department of Oncology, Faculty of Health Sciences, Ludwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, 87-100 Torun, Poland.
Department of Lung Diseases, Tuberculosis and Sarcoidosis, Kuyavian-Pomeranian Pulmonology Center, 85-326 Bydgoszcz, Poland.
Cancers (Basel). 2024 Feb 25;16(5):923. doi: 10.3390/cancers16050923.
Extracellular vesicles (EVs), including exosomes and microvesicles, together with apoptotic bodies form a diverse group of nanoparticles that play a crucial role in intercellular communication, participate in numerous physiological and pathological processes. In the context of cancer, they can allow the transfer of bioactive molecules and genetic material between cancer cells and the surrounding stromal cells, thus promoting such processes as angiogenesis, metastasis, and immune evasion. In this article, we review recent advances in understanding how EVs, especially exosomes, influence tumor progression and modulation of the microenvironment. The key mechanisms include exosomes inducing the epithelial-mesenchymal transition, polarizing macrophages toward protumoral phenotypes, and suppressing antitumor immunity. The therapeutic potential of engineered exosomes is highlighted, including their loading with drugs, RNA therapeutics, or tumor antigens to alter the tumor microenvironment. Current techniques for their isolation, characterization, and engineering are discussed. Ongoing challenges include improving exosome loading efficiency, optimizing biodistribution, and enhancing selective cell targeting. Overall, exosomes present promising opportunities to understand tumorigenesis and develop more targeted diagnostic and therapeutic strategies by exploiting the natural intercellular communication networks in tumors. In the context of oncology, regulatory therapy provides the possibility of reproducing the original conditions that are unfavorable for the existence of the cancer process and may thus be a feasible alternative to population treatments. We also review current access to the technology enabling regulatory intervention in the cancer process using exosomes.
细胞外囊泡(EVs),包括外泌体和微囊泡,与凋亡小体共同构成了一组多样的纳米颗粒,它们在细胞间通讯中发挥着关键作用,参与众多生理和病理过程。在癌症背景下,它们能够促使生物活性分子和遗传物质在癌细胞与周围基质细胞之间传递,从而促进血管生成、转移和免疫逃逸等过程。在本文中,我们综述了近期在理解EVs尤其是外泌体如何影响肿瘤进展和微环境调节方面的进展。关键机制包括外泌体诱导上皮-间质转化、使巨噬细胞极化为促肿瘤表型以及抑制抗肿瘤免疫。强调了工程化外泌体的治疗潜力,包括用药物、RNA疗法或肿瘤抗原装载外泌体以改变肿瘤微环境。讨论了目前用于其分离、表征和工程化的技术。当前面临的挑战包括提高外泌体装载效率、优化生物分布以及增强选择性细胞靶向性。总体而言,外泌体为通过利用肿瘤中天然的细胞间通讯网络来理解肿瘤发生以及开发更具针对性的诊断和治疗策略提供了有前景的机会。在肿瘤学背景下,调节疗法提供了重现不利于癌症进程存在的原始条件的可能性,因此可能是群体治疗的一种可行替代方案。我们还综述了当前使用外泌体对癌症进程进行调节干预的技术途径。