| Literature DB >> 33763118 |
Na Luan1,2, Yali Mu1,2, Jiayi Mu2, Yiquan Chen1,2, Xun Ye1,2, Qin Zhou1,2, Miaorong Xu2, Qun Deng2, Yeting Hu2, Zhe Tang3,4, Jianwei Wang1,2.
Abstract
Hypoxia plays a key role in colorectal cancer (CRC) metastasis, but its underlying mechanism remains largely unknown. Dicer1, an RNase, has been considered as a tumor regulator in many tumors. However, whether Dicer1 affects CRC progression under hypoxia remains uncertain. In this study, we found that Dicer1 expression was induced by hypoxia in CRC cells and it mediates hypoxia-induced CRC cell progression. Furthermore, we found that the expression of tRF-20-MEJB5Y13, a small non-coding RNA derived from tRNA, was increased under hypoxic conditions, and its upregulation by Dicer1 resulted in hypoxia-induced CRC cell invasion and migration. These results advance the current understanding of the role of Dicer1 in regulating hypoxia signals and provide a new pathway for the development of therapeutic interventions for inhibiting cancer progression.Entities:
Keywords: Dicer; colorectal cancer; epithelial-to-mesenchymal transition; hypoxia; tRNA-derived fragments
Year: 2021 PMID: 33763118 PMCID: PMC7982525 DOI: 10.3389/fgene.2021.638244
Source DB: PubMed Journal: Front Genet ISSN: 1664-8021 Impact factor: 4.599