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PLoS Pathog ; 13(7): e1006508, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28715488

ABSTRACT

Kaposi's sarcoma (KS) is a highly prevalent cancer in AIDS patients, especially in sub-Saharan Africa. Kaposi's sarcoma-associated herpesvirus (KSHV) is the etiological agent of KS and other cancers like Primary Effusion Lymphoma (PEL). In KS and PEL, all tumors harbor latent KSHV episomes and express latency-associated viral proteins and microRNAs (miRNAs). The exact molecular mechanisms by which latent KSHV drives tumorigenesis are not completely understood. Recent developments have highlighted the importance of aberrant long non-coding RNA (lncRNA) expression in cancer. Deregulation of lncRNAs by miRNAs is a newly described phenomenon. We hypothesized that KSHV-encoded miRNAs deregulate human lncRNAs to drive tumorigenesis. We performed lncRNA expression profiling of endothelial cells infected with wt and miRNA-deleted KSHV and identified 126 lncRNAs as putative viral miRNA targets. Here we show that KSHV deregulates host lncRNAs in both a miRNA-dependent fashion by direct interaction and in a miRNA-independent fashion through latency-associated proteins. Several lncRNAs that were previously implicated in cancer, including MEG3, ANRIL and UCA1, are deregulated by KSHV. Our results also demonstrate that KSHV-mediated UCA1 deregulation contributes to increased proliferation and migration of endothelial cells.


Subject(s)
Herpesvirus 8, Human/physiology , MicroRNAs/metabolism , RNA, Long Noncoding/genetics , RNA, Viral/metabolism , Sarcoma, Kaposi/genetics , Viral Proteins/metabolism , Cell Line , Herpesvirus 8, Human/genetics , Host-Pathogen Interactions , Humans , MicroRNAs/genetics , RNA, Long Noncoding/metabolism , RNA, Viral/genetics , Sarcoma, Kaposi/metabolism , Sarcoma, Kaposi/virology , Viral Proteins/genetics , Virus Latency
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