AI Article Synopsis
- Most human endogenous retroviruses (HERVs) are inactive due to mutations but still impact human health, particularly in diseases like cancer.
- This study identified 29 microRNAs from HERV sequences, focusing on miR-4454, which is upregulated in non-muscle-invasive bladder cancer (NMIBC) cells.
- Researchers found that miR-4454 reduces the expression of tumor suppressor genes, promoting the progression of NMIBC.
Article Abstract
Although most human endogenous retroviruses (HERVs) have been silenced and lost their ability to translocate because of accumulated mutations during evolution, they still play important roles in human biology. Several studies have demonstrated that HERVs play pathological roles in numerous human diseases, especially cancer. A few studies have revealed that long non-coding RNAs that are transcribed from HERV sequences affect cancer progression. However, there is no study on microRNAs derived from HERVs related to cancer. In this study, we identified 29 microRNAs (miRNAs) derived from HERV sequences in the human genome. In particular, we discovered that miR-4454, which is HERV-H-derived miRNA, was upregulated in non-muscle-invasive bladder cancer (NMIBC) cells. To figure out the effects of upregulated miR-4454 in NMIBC, genes whose expression was downregulated in NMIBC, as well as tumor suppressor genes, were selected as putative target genes of miR-4454. The dual-luciferase assay was used to determine the negative relationship between miR-4454 and its target genes, and , and they were confirmed to be promising target genes of miR-4454. Taken together, this study suggests that the upregulation of miR-4454 derived from HERV-H in NMIBC reduces the expression of the tumor suppressor genes, and , to promote NMIBC progression.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379226 | PMC |
| http://dx.doi.org/10.3390/genes14071410 | DOI Listing |
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