Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.
Division of Infectious Diseases, State Key Laboratory of Biotherapy and Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.
J Hematol Oncol. 2019 May 29;12(1):53. doi: 10.1186/s13045-019-0739-0.
The tumor microenvironment (TME) is an essential intrinsic portion of hepatocellular carcinoma (HCC) for the regulation of its origination, development, invasion, and metastasis. As emerging components of the tumor-host interaction, exosomes are increasingly recognized as professional carriers of information in TME and as pivotal molecular entities involved in tumorigenic microenvironment setup. However, much remains unknown about the role of the exosome communication system within TME in the development and progression of HCC. In this review, we focus on the roles and probable mechanisms of TME in HCC and show the exosome-based immune regulation in TME to promote HCC. Multiple processes are involved in HCC, including tumor survival, growth, angiogenesis, invasion, and metastasis. We also discuss the specific roles of exosomes in HCC processes by molding hospitable TME for HCC, such as providing energy, transmitting protumor signals, and evading inhibitory signals. In addition, exosomes induce angiogenesis by changing the biological characteristics of endothelial cells and directly regulating proangiogenic and propermeability factors. Furthermore, exosomes may lead to HCC metastatic invasion by epithelial-mesenchymal transformation, extracellular matrix degradation, and vascular leakage. Finally, we summarize the therapeutic usage of exosomes in the HCC microenvironment and attempt to provide a theoretical reference for modern antitumor agents designed to target these mechanisms.
肿瘤微环境(TME)是肝细胞癌(HCC)发生、发展、侵袭和转移的重要内在组成部分。作为肿瘤-宿主相互作用的新兴成分,外泌体越来越被认为是 TME 中信息的专业载体,也是参与肿瘤微环境形成的关键分子实体。然而,外泌体通讯系统在 TME 中在 HCC 发展和进展中的作用仍知之甚少。在这篇综述中,我们重点关注 TME 在 HCC 中的作用和可能的机制,并展示基于外泌体的 TME 免疫调节以促进 HCC。多个过程涉及 HCC,包括肿瘤存活、生长、血管生成、侵袭和转移。我们还通过塑造有利于 HCC 的 TME 来讨论外泌体在 HCC 过程中的具体作用,例如提供能量、传递促肿瘤信号和逃避抑制信号。此外,外泌体通过改变内皮细胞的生物学特性并直接调节促血管生成和通透性因子来诱导血管生成。此外,外泌体可能通过上皮-间充质转化、细胞外基质降解和血管渗漏导致 HCC 转移侵袭。最后,我们总结了外泌体在 HCC 微环境中的治疗用途,并试图为针对这些机制设计的现代抗肿瘤药物提供理论参考。