外泌体转运的非编码 RNA 重塑低氧肿瘤微环境。
Non-coding RNAs shuttled via exosomes reshape the hypoxic tumor microenvironment.
机构信息
Interdisciplinary Program in Cancer Biology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Cancer Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
出版信息
J Hematol Oncol. 2020 Jun 5;13(1):67. doi: 10.1186/s13045-020-00893-3.
Exosomes are small extracellular vesicles secreted by almost all the cells. Molecular cargos of exosomes can partially reflect the characteristics of originating cells. Exosome-mediated cell-to-cell interactions in the microenvironment are critical in cancer progression. Hypoxia, a key pro-cancerous feature of the tumor microenvironment, alters the releasing and contents of exosomes. A growing body of evidence shows that hypoxia induces more aggressive phenotypes in cancer. Of note, non-coding RNAs shuttled in hypoxic tumor-derived exosomes have been demonstrated as fundamental molecules in regulating cancer biology and remodeling tumor microenvironment. Furthermore, these hypoxic tumor-derived exosomal non-coding RNAs can be detected in the body fluids, serving as promising diagnostic and prognostic biomarkers. The current review discusses changes in cancer behaviors regulated by exosomes-secreted non-coding RNAs under hypoxic conditions.
外泌体是几乎所有细胞分泌的小细胞外囊泡。外泌体的分子货物可以部分反映来源细胞的特征。外泌体介导的微环境中的细胞间相互作用在癌症进展中至关重要。缺氧是肿瘤微环境中促进癌症发生的关键特征,改变了外泌体的释放和内容物。越来越多的证据表明,缺氧会诱导癌症表现出更具侵袭性的表型。值得注意的是,在缺氧肿瘤衍生的外泌体中转运的非编码 RNA 已被证明是调节癌症生物学和重塑肿瘤微环境的基本分子。此外,这些缺氧肿瘤衍生的外泌体非编码 RNA 可以在体液中检测到,作为有前途的诊断和预后生物标志物。本综述讨论了在缺氧条件下由外泌体分泌的非编码 RNA 调节的癌症行为变化。