Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Operating Room, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Cancer Biomark. 2020;29(3):317-326. doi: 10.3233/CBM-201518.
MicroRNAs (miRNAs) have been validated to play prominent roles in the occurrence and development of anaplastic thyroid carcinoma (ATC). miR-199a-5p was previously reported to act as a tumor suppressor or oncomiRNA in various types of cancer. However, its accurate expression, function, and mechanism in ATC remain unclear. Here, we find that miR-199a-5p is significantly downregulated in ATC tissues compared with adjacent non-cancerous tissues. Overexpression of miR-199a-5p significantly inhibits migration and invasion of ATC cells in vitro, and lung metastasis in vivo. Importantly, miR-199a-5p suppresses epithelial-mesenchymal transition (EMT) both in vitro and in vivo by targeting Snail. Taken together, this study reveals that miR-199a-5p is critical to the EMT progression in ATC cells. Targeting the pathway described here may be a novel approach for inhibiting metastasis of ATC.
微小 RNA(miRNAs)已被证实在间变性甲状腺癌(ATC)的发生和发展中发挥重要作用。miR-199a-5p 先前被报道在多种类型的癌症中作为肿瘤抑制因子或癌基因发挥作用。然而,其在 ATC 中的准确表达、功能和机制仍不清楚。在这里,我们发现 miR-199a-5p 在 ATC 组织中明显下调,与相邻的非癌组织相比。miR-199a-5p 的过表达可显著抑制 ATC 细胞在体外的迁移和侵袭,以及体内的肺转移。重要的是,miR-199a-5p 通过靶向 Snail 在线粒体和体内均抑制上皮间质转化(EMT)。综上所述,本研究揭示了 miR-199a-5p 在 ATC 细胞的 EMT 进展中至关重要。靶向这里描述的通路可能是抑制 ATC 转移的一种新方法。