Ren Xudong, Zhou Yu, Luo Yunling, Wang Chaoqun, Pan Anna, Ju Yanqin, Sun Haoting, Lin Zhifei, Hu Beiyuan, Sun Guangzheng, Zhu Wenwei, Hong Liang
Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Department of Infectious Diseases, The Third Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Gastroenterol Res Pract. 2022 Apr 6;2022:4589163. doi: 10.1155/2022/4589163. eCollection 2022.
Interleukin-6 (IL-6), an important inflammatory cytokine, is a key factor regulating cancer metastasis. Cancer cells can modulate their tumorigenic abilities by sorting specific microRNAs (miRNAs) as exosomes into the tumor microenvironment. The relationship between IL-6 and exosomal miRNAs related to hepatocellular carcinoma (HCC) metastasis remains to be elucidated. We examined the metastatic ability of HCC cells after IL-6 treatment and found that miR-133a-3p was sorted into exosomes after IL-6 stimulation and was subsequently released into the tumor microenvironment. In vitro analysis confirmed that exosomal miR-133a-3p acted as a tumor suppressor in HCC. Bioinformatic analysis revealed several signaling pathways and hub genes (CREB1, VCP, CALM1, and YES1) regulated by miR-133a-3p. Survival curves further verified the important roles of hub genes in the prognosis of patients with HCC. It is envisaged that the IL-6/miR-133a-3p axis may be related to the activation of CREB1, VCP, CALM1, and YES1. Our findings provide new insights into the role of exosomal miRNA-mediated tumor progression under inflammatory conditions.
白细胞介素-6(IL-6)是一种重要的炎症细胞因子,是调节癌症转移的关键因素。癌细胞可通过将特定的微小RNA(miRNA)作为外泌体分选到肿瘤微环境中,来调节其致瘤能力。IL-6与肝细胞癌(HCC)转移相关的外泌体miRNA之间的关系仍有待阐明。我们检测了IL-6处理后HCC细胞的转移能力,发现miR-133a-3p在IL-6刺激后被分选到外泌体中,随后释放到肿瘤微环境中。体外分析证实,外泌体miR-133a-3p在HCC中起肿瘤抑制作用。生物信息学分析揭示了受miR-133a-3p调控的几种信号通路和枢纽基因(CREB1、VCP、CALM1和YES1)。生存曲线进一步验证了枢纽基因在HCC患者预后中的重要作用。据推测,IL-6/miR-133a-3p轴可能与CREB1、VCP、CALM1和YES1的激活有关。我们的研究结果为炎症条件下外泌体miRNA介导的肿瘤进展作用提供了新的见解。