| Literature DB >> 29620929 |
Liujun Chen1, Lang Chen1, Luoshiyuan Zuo2, Ziang Gao1, Yingying Shi3, Peipei Yuan1, Song Han1,4, Jun Yin1,4, Biwen Peng1,4, Xiaohua He1,4, Wanhong Liu1,4.
Abstract
HIV is the causative pathogen of AIDS, which has generated worldwide concern. Long noncoding RNAs (lncRNAs) are a rising star in virus-host cross-talk pathways; they are differentially expressed during many viral infections and are involved in multiple biological processes. Currently, lncRNA growth arrest-specific transcript 5 (GAS5) is known to be downregulated during HIV-1 infection. However, the functions and mechanisms of GAS5 in HIV-1 infection remain largely unknown. In this report, it was found for the first time that GAS5 could inhibit HIV-1 replication. Interestingly, using bioinformatics analyses (with Genomica and starBase.v2.0), GAS5 was found to potentially interact with miR-873. It was further verified that GAS5 could suppress miR-873. Moreover, miR-873 could promote HIV-1 replication. Together, these results not only suggest that GAS5 may inhibit HIV-1 replication through interaction with miR-873 but the results may also provide novel biomarkers for antiviral drugs or potential targets for future therapeutics for HIV/AIDS.Entities:
Keywords: GAS5; HIV; lncRNAs; miR-873
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Year: 2018 PMID: 29620929 DOI: 10.1089/AID.2017.0177
Source DB: PubMed Journal: AIDS Res Hum Retroviruses ISSN: 0889-2229 Impact factor: 2.205