Epstein-Barr virus (EBV) is an oncogenic virus that ubiquitously establishes life-long persistence in humans. To ensure its survival and maintain its B cell transformation function, EBV has developed powerful strategies to evade host immune responses. Emerging evidence has shown that microRNAs (miRNAs) are powerful regulators of the maintenance of cellular homeostasis. In this review, we summarize current progress on how EBV utilizes miRNAs for immune evasion. EBV encodes miRNAs targeting both viral and host genes involved in the immune response. The miRNAs are found in two gene clusters, and recent studies have demonstrated that lack of these clusters increases the CD4+ and CD8+ T cell response of infected cells. These reports strongly indicate that EBV miRNAs are critical for immune evasion. In addition, EBV is able to dysregulate the expression of a variety of host miRNAs, which influence multiple immune-related molecules and signaling pathways. The transport via exosomes of EBV-regulated miRNAs and viral proteins contributes to the construction and modification of the inflammatory tumor microenvironment. During EBV immune evasion, viral proteins, immune cells, chemokines, pro-inflammatory cytokines, and pro-apoptosis molecules are involved. Our increasing knowledge of the role of miRNAs in immune evasion will improve the understanding of EBV persistence and help to develop new treatments for EBV-associated cancers and other diseases..
Citation: Lielian Zuo, Wenxin Yue, Shujuan Du, Shuyu Xin, Jing Zhang, Lingzhi Liu, Guiyuan Li, Jianhong Lu. An update: Epstein-Barr virus and immune evasion via microRNA regulation [J]. VIROLOGICA SINICA, 2017, 32 (3) : 175-187 https://doi.org/10.1007/s12250-017-3996-5
Received: 8 April, 2017; Accepted: 12 June 2017; Published online: 26 June 2017
Copyright: © The Author(s) 2017. This article is published with open access at Springerlink.com
Data Availability: All relevant data are within the paper and its Supporting Information files.
Epstein-Barr virus (EBV) was the first confirmed oncogenic virus capable of infecting humans, and it belongs to the human herpesvirus family. It is associated with several lymphocytic and epithelial malignancies in humans such as Burkitt’s lymphoma and nasopharyngeal carcinoma (NPC) (Young and Rickinson, 2004; Luo and Ou, 2015; Tsang and Tsao, 2015). EBV can establish life-long latent infections and, if it not cleared by the host immune system, it can contribute to cancer development, suggesting that it has evolved the ability to escape recognition by the host’s innate immune system. Similarly, immunocompromised individuals, such as HIV and post-transplant patients, are prone to develop EBV-associated lymphomas, implying that when there is less host immune surveillance, the function of EBV changes. Since EBV pathogenesis consists of a virus-host interaction, both viral and host factors are involved in the viral immune evasion strategies. In primary EBV infections, cellular immunity is the main host immune response.
MicroRNAs (miRNAs) are a type of small non-coding RNA molecule, consisting of about 18 to 22 nucleotides. The mature single-stranded miRNAs bind to the 3'-untranslated region (UTR) of target mRNAs so as to inhibit the expression of target genes (Buchan and Parker, 2007; Jia et al., 2014). miRNAs have emerged as major transcriptional regulators of gene expression related to critical biological processes including cellular proliferation, differentiation, and viral immune evasion, and they are known to contribute to the development of cancers (Adams et al., 2014; Tsang and Tsao, 2015). In latent EBV infections involving host functional immunity, EBV expresses limited levels of protein but high levels of noncoding RNAs, including miRNAs. This indicates that the miRNAs are related to viral immune evasion (Jia et al., 2014; Zeng et al., 2014). EBV expresses about 40 mature miRNAs that target viral or cellular genes to induce different functions. In addition, viral proteins also regulate host miRNAs. EBV-encoded and EBV-regulated miRNAs appear to play an important role in immune evasion (Piedade and Azevedo-Pereira, 2016).
Accumulating studies have highlighted the link between the immune system and inflammatory tumor microenvironments. Tumors are surrounded and infiltrated by a variety of cell types, including fibroblasts, immune cells, and vascular endothelial cells, which can interact with each other to generate the tumor microenvironment. This complex microenvironment is thought to be regulated by the tumor cells in order to promote their survival and replication. The inflammatory tumor microenvironment plays a role in cancer development. EBV-encoded latent membrane proteins (LMP1 and LMP2A), which are able to induce the expression of multiple molecules linked to inflammation and the immune response, may act as targets of EBV-encoded miRNAs (Ressing et al., 2015). The molecules in the microenvironment constitute potential targets for anticancer and antiviral drug development (De Clercq and Li, 2016). This review will update the current knowledge about both EBV-encoded and EBV-dysregulated host-encoded miRNAs involved in viral immune evasion, the inflammatory response, and the tumor microenvironment in EBV-related carcinogenesis.
BIOGENESIS OF EBV miRNAs
EBV was the first virus that encodes miRNAs to be discovered, and the biogenesis of these miRNAs is similar to the biogenesis of cellular miRNAs (Kim and Lee, 2012). The EBV miRNAs are encoded in two main clusters: the EBV BamH I fragment H rightward open reading frame 1 (BHRF1) cluster and the BamH I fragment A rightward transcript (BART) cluster. They are mainly transcribed by RNA polymerase II (pol II) to produce stem-loop structures, and they are subjected to sequential processing. The host endonuclease Drosha and DiGeorge syndrome chromosomal region 8 (DGCR8) complex cleaves the primary miRNA, resulting in a precursor miRNA, which has an imperfect hairpin structure and which is transported from the nucleus to the cytoplasm. Subsequently, the host protein Dicer further processes the precursor miRNA in the cytoplasm to generate the mature miRNA (Kim and Lee, 2012).
EBV-ENCODED miRNAs REGULATE THE IMMUNE RESPONSE BY TARGETING VIRAL PROTEINS
EBV miRNAs are expressed in EBV-positive cells such as the primary effusion lymphoma cell line (PEL-1) and EBV-positive Burkitt’s lymphoma and nasopharyngeal carcinomas (NPC). EBV BHRF1 encodes three miRNA precursors (EBV-miR-BHRF1-3), generating four mature EBV miRNAs. The BART region encodes 22 miRNA precursors (EBV-miR-BART1-22), producing about 40 mature miRNAs (Lo et al., 2012; Barth et al., 2011).
EBV miRNAs can target both cellular and viral mRNAs to evade the host immune response (as summarized in Figure 1, 2 and Table 1, 2). Viral proteins such as LMP1 and LMP2A have been found to be associated with EBV immune evasion (Ressing et al., 2015). LMP1 triggers multiple pathways such as the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB), activator protein-1 (AP-1), Janus kinase (JAK)/signal transducer and activator of transcription (STAT) and phosphatidylinositol-specific phospholipase C (P1-PLC)-protein kinase C (PKC) signaling pathways to upregulate or downregulate a series of molecules related to the immune response (Dukers et al., 2000; Ding et al., 2007; Zheng et al., 2007). For example, LMP1 stimulates the receptor-interacting protein (RIP) and RIP-dependent K63-linked ubiquitination of interferon regulatory factor 7 (IRF7), which plays an important role in immune defense (Huye et al., 2007; Li et al., 2007). Four EBV miRNAs (miR-BART3, miR-BART5, miR-BART16, and miR-BART17) directly target LMP1, and thereby indirectly inhibit surface expression of certain immune co-receptors and adhesion molecules. This helps to alter the balance of LMP1’s growth-promoting and pro-apoptotic actions (Lo et al., 2007; Skalsky et al., 2014; Verhoeven et al., 2016). Unlike the four abovementioned EBV miRNAs, miR-BART9 is involved in maintaining LMP1 mRNA stability in growing T cell lymphomas, though it does not target LMP1 directly (Lo et al., 2007). The targeting of LMP2A by miR-BART22 in EBV latent infections can lead to immune surveillance escape, cellular invasion, and metastasis (Lung et al., 2009; Kanda et al., 2015).
In addition to LMP1 and LMP2A, other viral genes, such as early genes, may be targeted by EBV miRNAs in order to maintain the viral latent infection and inhibit lytic replication. EBV miR-BART2-5p targets BALF5, while miR-BART20-5p targets BZLF1 and BRLF1 (Barth et al., 2008; Jung et al., 2014). EBV miR-BART6-5p inhibits the expression of Epstein-Barr virus nuclear antigen 2 (EBNA2), which is a key activator that causes the latent infection to change to bring about lytic replication (Iizasa et al., 2010). Thus, it can be seen that EBV has evolved a set of miRNAs to effectively maintain the latent infection.
EBV-ENCODED miRNAs REGULATE THE IMMUNE RESPONSE BY TARGETING CELLULAR IMMUNE-RELATED GENES
Viral miRNAs can also directly target cellular mRNAs involved in the host immune response (Figure 1). Both miR-BHRF1-3 and miR-BART17 target transporter associated with antigen processing 2 (TAP2), which is a mediator of antigenic peptide transportation and EBV epitope presentation (Albanese et al., 2016). EBV miR-BHRF1-2 has a role in the inhibition of PR domain-containing protein 1 (PRDM1) in lymphoblastoid cell lines (Ma et al., 2016). PRDM1 is a master regulator of B cell terminal differentiation and has been identified as a tumor suppressor gene in aggressive lymphomas such as diffuse large B cell lymphoma (DLBCL). The major histocompatibility complex class I-related chain B (MICB) is targeted by miR-BART2-5p, preventing natural killer (NK) cells from recognizing EBV-infected cells. In virus infections and tumor proliferation, MICB expression increases, and it has been found to activate NK and T cells, thereby initiating the immune reaction (Diefenbach et al., 2000; Nachmani et al., 2009; Lisnic et al., 2010; Liu et al., 2012). EBV miR-BART1, miR-BART2, and miR-BART22 co-target interleukin-12 (IL-12), leading to decreased T cell differentiation, activation, and recognition at different stages of infection and malignant disease (Albanese et al., 2016). EBV miR-BART3-3p weakens the cytotoxic effect by inhibiting the expression of importin 7 (IPO7), which regulates T cells activation and immune tolerance (Dolken et al., 2010). MiR-BART20-5p and miR-BART8 target and alter interferon-γ (IFN-γ) secretion in EBV-positive tumors (Huang and Lin, 2014). This may be why many immune cells (such as CD8+ and CD4+ T cells, B cells, NK cells, and macrophages) can be found in NPC, but EBV-specific cytotoxic T lymphocytes (CTLs) are incapable of increasing cell-mediated immunity.
In addition, CXC-chemokine ligand 11 (CXCL11) can be targeted by miR-BHRF1-3, which in turn shields EBV-infected B cells from CTLs (Xia et al., 2008). Recently, EBV miR-BHRF1-2-5p has been reported to target mucosa-associated lymphoid tissue lymphoma transport protein 1 (MALT1), a key regulator of immune homeostasis (Wang et al., 2017). EBV miR-BART16 interferes with the type I IFN signaling pathway by directly targeting cAMP response element-binding protein (CREB)-binding protein (CREBBP), a key transcriptional coactivator in IFN signaling (Hooykaas et al., 2017).
Therefore, EBV-encoded miRNAs impair the recognition and clearance functions of the host immune system, thus increasing viral pathogenesis. The identification of target genes of EBV miRNAs may help to unveil the role of EBV in immune evasion.
LACK OF VIRAL miRNA GENE CLUSTERS IN THE EBV GENOME INCREASES THE HOST IMMUNE RESPONSE
EBV miRNAs are encoded by two gene clusters in the viral genome. The narrow spaces between the miRNAs indicate that there is interplay between them that influences their function and expression. The transcription order of the viral miRNAs remains unknown. A recent study found that the distance between two miRNAs in the same cluster may affect the miRNA expression levels, independent of the seed regions (Haar et al., 2016). The EBV BHRF1 miRNA cluster promotes B cell transformation. Increasing the distance between miR-BHRF1-2 and miR-BHRF1-3 in EBV enhances the expression of miR-BHRF1-3 but reduces the transforming potential of the BHRF1 miRNAs in B cells (Haar et al., 2016).
Therefore, studies on the miRNA clusters in the context of the whole viral genome may be valuable for elucidating the viral miRNA functions. To reach this goal, EBV mutants that lack the miRNA clusters may help. Several approaches have recently demonstrated that lack of the miRNA clusters in EBV mutants increases the CD4+ and CD8+ T cell host immune response, strongly supporting the conclusion regarding the important roles of EBV miRNAs in immune evasion.
Wolfgang Hammerschmidt’s group has conducted multiple key studies on EBV mutants. Using EBV mutants that lacked the miRNA clusters, they demonstrated that the EBV miRNAs inhibit antiviral CD4+ T cell responses by targeting IL-12 and peptide processing (Tagawa, 2016). At the same time, EBV miRNAs reduce immune surveillance by virus-specific CD8+ T cells (Albanese et al., 2016). The findings are helpful to explain the abundance of miRNAs in the complex virus, and to clarify how EBV can escape elimination for the lifetime of its host in spite of intense adaptive host immune responses.
In another EBV mutant study, knock-out of the BHRF1 cluster increased the production of phosphatase and tensin homolog (PTEN) and p27, implying that BHRF1 miRNAs are associated with a propensity to promote neoplastic cell transformation, which is beneficial for long-term persistence of the virus in the host.
All these results support the importance of EBV miRNAs for immune evasion. EBV miRNAs use multiple distinct pathways, allowing the virus to evade host immune surveillance (Bernhardt et al., 2016). Understanding of the functions of EBV miRNAs provides novel insights into the elaborate systems that EBV has evolved to successfully establish lifelong infections. EBV miRNA-mediated interference may contribute to the maintenance of EBV-positive tumors.
EBV LATENT PROTEINS DYSREGULATE HOST miRNAs TO REGULATE THE IMMUNE RESPONSE
In EBV-associated cancers, a few EBV latent proteins can be detected. These proteins (LMP1, LMP2A, EBNA1, EBNA2, EBNA3A, and EBNA3C) induce or inhibit the expression of a variety of endogenous miRNAs, which regulates the immune response (as summarized in Table 2 and Figure 2).
Multiple cellular miRNAs that are dysregulated by EBV can be induced in innate immune cells. Among them, miR-155, miR-146a, and miR-21 are associated with inflammation and immune modulation (Zhu et al., 2013; Zeng et al., 2015; Zhang et al., 2015a). MiR-155 suppresses Toll-like receptors (TLRs) and triggers an immune response (Sun et al., 2012). In the presence of a TLR3 ligand, the expression level of miR-21 can be upregulated in a NPC cell line (C666-1) and tissues (Miao et al., 2015). MiR155 also mediates an increase in IL-10 expression by B lymphocytes, resulting in the inhibition of CD8+ T cell activation (Sun et al., 2012). By targeting C-C motif chemokine ligand 22 (CCL22), miR-34a is involved in immune escape and stromal cell recruitment (Yang et al., 2012). STAT3 can promote the expression of a large number of immunosuppressive factors such as IL-10 (Yu et al., 2016). In turn, these factors activate STAT3. STAT3 is able to transcriptionally bind to the promoter of miR-146a, which is a key regulator of innate antiviral responses (Sun et al., 2015). MiR-146a also targets two immune-associated genes, interleukin-1 receptor-associated kinase 1 (IRAK1) and TNF receptor-associated factor 6 (TRAF6). IRAK1 is a key innate immune signal molecule (Li et al., 2010b; Saba et al., 2014). It participates in signaling cascade regulation associated with TLR/IL-1R, changing the expression of inflammatory factors such as tumor necrosis factor-α (TNF-α) and type I IFNs. TRAF6 is involved in the cellular immune response by interacting with TLRs and the IFN-γ signal transduction pathway (Yang et al., 2007; Li et al., 2010b). Let-7a is upregulated by EBNA1 and has been shown to directly alter cell cycle progression and pro-inflammatory cytokine production. The let-7a expression and IL-6 production is significantly decreased by the depletion of E2F2 or NF-κB in immune-stimulated cells (Cho et al., 2015). MiR-222, miR-223, the miR-17~92 cluster, and miR-155 are associated with the differentiation of T cells (Riley et al., 2012; Poole and Sinclair, 2015; Saki et al., 2015). EBV-encoded EBNA2 induces the expression of miR-21, consequently promoting B cell transformation and driving the antiviral immune response (Rosato et al., 2012; Zhu et al., 2013). The upregulation of miR-127 in EBV-positive Burkitt’s lymphoma may cause the downregulation of the B cell markers, B lymphocyte-induced maturation protein 1 (BLIMP-1) and X-box binding protein 1 (XBP-1) (Onnis et al., 2012).
These miRNAs dysregulated by EBV proteins may serve as the tumor promotors. EBV utilizes multiple host miRNAs to adapt to the host immune response and promote immune evasion. In-depth studies of this aspect may provide a more complete understanding about the pathogenic mechanism employed by EBV.
EBV miRNAs SUPPRESS APOPTOSIS OF INFECTED CELLS TO MAINTAIN THE EBV LATENT STATUS AND IMMUNE EVASION
In general, EBV remains latent in tumors and expresses a limited repertoire of latent proteins to avoid host immune surveillance. Apoptosis may expedite EBV-associated tumor cell death and is detrimental for the viral latent infection and EBV evasion of the host immune attack. Thus, the virus has evolved strategies to suppress the apoptosis of infected cells. Several studies have directly or indirectly revealed that EBV miRNAs are involved in apoptosis suppression. For instance, in EBV-associated gastric carcinomas, miR-BART 20-5p not only targets the EBV immediate early genes BRLF1 and BZLF1, but also Bcl-2-associated death promoter (BAD) in the caspase-3-dependent apoptosis pathway (Jung et al., 2014; Kim et al., 2015).
In the BART cluster, an interference approach revealed that at least seven BART miRNAs are involved in anti-apoptotic activity in NPC by targeting multiple pro-apoptotic cellular genes. Naturally, the BHRF1 miRNA cluster is located at the BHRF1 gene, and the protein product of this gene has anti-apoptotic properties. If B cells are infected with a mutant EBV lacking the BHRF1 miRNAs, they may undergo apoptosis to a greater extent and grow more slowly compared to B cells infected with an intact virus. The BHRF miRNAs also regulate the expression of PTEN, p27, and a Bcl-2 homolog, allowing the expansion of the virus B cell reservoir during the early infection without increasing long-term immune pressure (Bernhardt et al., 2016). In NPC, miR-BART5 can target p53-upregulated modulator of apoptosis (PUMA) to inhibit cellular apoptosis (Choy et al., 2008). EBV BART miRNA Cluster I or II directly inhibit the pro-apoptotic protein, Bim (Marquitz et al., 2011). The translocase of outer mitochondrial membrane 22 (TOMM22), which serves as a receptor for the Bcl-2-associated X (BAX), is targeted by miR-BART16. Antisense knockdown of TOMM22 has been shown to inhibit the association of the pro-apoptotic protein Bcl-2-associated X (BAX) with mitochondria and thus prevent BAX-induced apoptosis (Bellot et al., 2007; Dolken et al., 2010). MiR-BART15-3p can induce apoptosis partially by inhibiting an apoptosis inhibitor, BIR repeat-containing ubiquitin-conjugating enzyme (BRUCE) (Choi et al., 2013). These reports show that EBV miRNAs help to maintain the viral latent status in the infected cells by preventing the host immune response.
EBV REGULATES THE INFLAMMATORY TUMOR MICROENVIRONMENT VIA miRNAs
The regulation of cellular or viral protein expression by EBV-encoded and EBV-regulated miRNAs may result in changes in cellular pathways, creating a virus-friendly microenvironment. LMP1 regulates the tumor microenvironment by inducing the NF-κB signaling pathway (Yu et al., 2012). As mentioned above, four EBV BART-miRNAs co-target LMP1, potentially contributing to the modulation of the tumor microenvironment. It has also been shown that EBV-miR-BART11 targets forkhead box P1 (FOXP1), a key molecule involved in differentiation of monocytes to macrophages (Song et al., 2016). In EBV-associated NPC and gastric carcinomas, the inhibition of FOXP1 induces the differentiation of tumor-associated macrophages (TAMs) and secretion of inflammatory cytokines into the tumor microenvironment.
EBV miR-BART15 targets the NOD-like receptors protein 3 (NLRP3) and inhibits the inflammasome production of IL-1β (Haneklaus et al., 2012). NLRP3 is one of the best-studied NLRs, which monitor intracellular homeostatic molecules. Many cell types require NLRP3 inflammasome priming, such as stimulation with a TLR ligand. As mentioned above, EBV-related miRNAs influence IL-6 signaling. IL-6, a pro-inflammatory factor secreted by immune cells, is able to promote the secretion of miR-21 and miR-29b by tumor cells, and the miRNAs in turn induce the expression of IL-6 (Patel and Gooderham, 2015). Downregulation of IPO7 by miR-BART3 in macrophages has been shown to reduce IL-6 production upon lipopolysaccharide challenge (Yang et al., 2009). In the pathogenesis of inflammatory diseases (including tumors and infections), miR-21 can act as an immune response circuit switch in order to control the balance between the initial pro-inflammatory response and the anti-inflammatory response (Sheedy, 2015).
Matrix metalloproteinase-2 and -9 (MMP2 and MMP9), which are miR-29b targets, may be involved in extracellular matrix remodeling and inhibition of epithelial-mesenchymal transition (Chou et al., 2013). The miR-203 inhibited by EBV-LMP1 targets IL-8, which is a chemotaxis cytokine and immune response mediator (Yu et al., 2011; Yu et al., 2012; Qu et al., 2015). EBV-induced miR-155 and miR-146a are also important molecules in the regulation of the inflammatory reaction (Zhang et al., 2015a; Yang et al., 2016; Bitar et al., 2017). EBNA1-induced miR-let-7a is a potential mediator of the inflammatory tumor microenvironment because miR-let-7a reduces the expression of inducible nitric oxide synthase (iNOS) and IL-6, and enhances the expression of IL-4 and IL-10 in microglia (Chen et al., 2007; Mansouri et al., 2014; Cho et al., 2015).
Cells can secrete multiple types of membrane vesicles, including exosomes, which are the best-characterized membrane vesicles. Exosomes are vesicles of 50–100 nm in size that are over-produced by most proliferating cell types during normal states, pathological states (such as cancer), and states such as pregnancy. Exosomes contain a wide variety of proteins, lipids, RNAs, non-transcribed RNAs, miRNAs, and small RNAs (Yin et al., 2013; Becker et al., 2016). Ongoing efforts have shown that miRNAs are secreted into tumor microenvironments to regulate cancer cell proliferation, migration, immune response, intercellular communication, and stromal modification, thereby promoting tumor growth and progression (Meckes et al., 2010; Zhang et al., 2015b; Li et al., 2016). EBV-regulated miRNAs and viral proteins can be secreted in exosomes to regulate the tumor microenvironment. It is speculated that tumor cells inhibit the host immune response by transporting exosomes containing EBV miRNAs to nearby cells or immune cells.
EBV-positive lymphoblastoid cell lines and NPC cells contain EBV BART miRNAs. The BART miRNAs secreted by NPC cells have enough stability to diffuse from the tumor site to the peripheral bloodstream, as well as to other non-infected cells. In EBV-positive NPC, exosomes containing several viral miRNAs, including miR-BART4, miR-BART7, miR-BART16, miR-BART9, miR-BART12 and miR-BART13, have been shown to be transported to adjacent endothelial cells (Pegtel et al., 2010). EBV-transformed lymphoblastoid B cells also secrete several viral miRNAs, including miR-BHRF1-1, miR-BHRF1-2, miR-BART1-3p, miR-BART1-5p, and miR-BART2-5p (Meckes et al., 2010). EBV-infected B lymphocytes are able to secrete miR-BART15 (Choi et al., 2013). The exosomal miR-BART15 provides a favorable microenvironment for the growth of EBV-associated tumors. This evidence shows that miRNAs are utilized by EBV for cell-to-cell communication and expanding the influence of the virus.
As described above, some viral proteins such as LMP1 are regulators of the immune response. LMP1 can be packaged into exosomes (Ceccarelli et al., 2007). Exosomes can deliver viral proteins to recipient cells such as epithelial, endothelial, and fibroblast cells (Meckes et al., 2010). It is noteworthy that LMP1 is not expressed in all the cells of EBV-associated tumors (Haneklaus et al., 2012). However, through exosomal transmission, viral oncoproteins can induce immune dysfunction in neighboring or even distant EBV-negative cells, providing a favorable microenvironment for the growth and migration of EBV-associated cancers.
EBV-ENCODED AND EBV-DYSREGULATED miRNAs ARE POTENTIAL BIOMARKERS AND THERAPEUTIC TARGETS
In the above mentioned miRNA studies, a series of EBV-encoded and EBV-dysregulated miRNAs have been shown to be potential clinical targets. EBV miR-BART1-5p and BART1-3p are dramatically increased in the N2-3 stages or advanced stages (III–IV) of NPC (Cai et al., 2015; Zheng et al., 2016). The levels of both miR-BART7 and miR-BART13 in NPC plasma are found to be present at distinct levels among patients with different stages of NPC, with elevated levels among patients with advanced disease. An analysis of 41 NPC patients before and after radiotherapy showed that miR-BART7 and miR-BART13 were diminished after treatment, suggesting a potential use for them in terms of NPC serological diagnosis and prediction of treatment efficacy (Zhang et al., 2015). The overexpression of EBV-miRBART10-3p in patients with NPC is significantly associated with poor disease-free and overall survival (Yan et al., 2012). These findings suggest that the effectiveness of current NPC treatments may be a result of the modulation of miRNA expression. In addition, miR-BART1-5p, miR-BART4-5p, and miR-BART20-5p are readily detectable in EBV-associated gastric carcinoma tissues, and the expression level of BART20-5p may predict relapse among these patients (Kang et al., 2017).
A study revealed a significant correlation between miR-183 and the NPC N stages (Tang et al., 2012). In 16 patients with non-keratinizing undifferentiated NPC, the miR-146a expression level was significantly elevated and may be useful as an indicator of NPC development (Zhao et al., 2012). Low expression of miR-204 is closely correlated with EBV infection status, lymph node metastasis, and more advanced clinical stages (Ma et al., 2014). There is a negative correlation between plasma miRNA expression and cancer progression, with miR-21 expression levels being significantly associated with the NPC T and N stages (Liu et al., 2013). In serum samples from patients with DLBCL, miR-21 expression levels are positively correlated with poor overall survival, thereby acting as an independent prognostic marker of overall survival in patients with DLBCL (Li et al., 2015). As described above, miR-155 has a crucial role in the immune response and inflammation. The miR-155 is upregulated in several malignancies and is associated with poor prognosis, thus it may be useful as a diagnostic and prognostic biomarker (Hanne et al., 2016; Due et al., 2016).
In addition, functional miRNAs in exosomes have been recognized as potentially stable cancer biomarkers. The miR-21 is found in many types of exosomes including tumor- and immunocyte-derived exosomes (Fabbri et al., 2012; Tian et al., 2014). Exosomal miRNAs such as miR-BART7-3p are usually stable, making them potentially ideal biomarkers (Gourzones et al., 2010). EBV BART miRNAs are secreted by NPC cells, with enough stability to diffuse from the tumor site to the peripheral bloodstream at levels that are detectable in plasma samples. Our increasing knowledge about the role of miRNAs in immune evasion will prove useful for understanding EBV persistence and developing improved treatments for EBV-associated cancers and other diseases.
EBV miRNAs are able to change the expression of a series of genes to regulate immune evasion. They also play a powerful role in regulating cancer progression via construction and modification of the microenvironment. EBV-encoded and EBV-dysregulated miRNAs are critical regulators of cellular gene expression associated with innate and adaptive immunity. The information presented in this review is summarized in Figure 3. Emerging evidence has demonstrated that exosomes play important roles in intracellular communication associated with cancer development. EBV-positive tumor cells secrete exosomes containing EBV-associated molecules such as miRNAs and viral proteins. Further studies of EBV-encoded and EBV-regulated miRNAs will be of great significance for the identification of the in-depth immunological mechanisms underlying EBV pathogenesis. The development of new treatments should place more emphasis on identifying potential target miRNAs to improve the effectiveness and personalization of EBV treatment.
BAD, Bcl-2-associated death promoter; BALF5, Viral DNA polymerase gene; BRLF1, EBV immediate early gene; BRUCE, BIR repeat-containing ubiquitin-conjugating enzyme; BZLF1, EBV immediate early gene; CBP, CREB binding protein; CCL17, Chemokine (C-C motif) ligand 17; CCL22, Chemokine (C-C motif) ligand 22; CTSB, Cathepsin B; CXCL-11, CXC-chemokine ligand 11; DGCR8: DiGeorge syndrome chromosomal region 8; DNAM-1, CD226 molecule; EBF1, Early B-cell factor 1; EBNAs, Epstein-Barr virus nuclear antigens; EBNA1, Epstein-Barr virus nuclear antigen 1; EBNA2, Epstein-Barr virus nuclear antigen 2; EBNA3A/EBNA3C, Epstein-Barr virus nuclear antigen 3A/3C; ICAM, Intercellular adhesion molecule; IFI30, Lysosomal thiol reductase; IFN-β: Interferon-β; IFN-γ: Interferon-γ; IFN-α: Interferon-α; IL-1β, Interleukin-1β; IL-6, Interleukin-6; IL-8, Interleukin-8; IL-10, Interleukin-10; IL-12, Interleukin-12; IL-12β, Interleukin-12 subunit beta; IPO7, Importin-7; IRF3, Interferon regulatory factor 3; IRF7, Interferon regulatory factor 7; LGMN, Legumain; LMP1, Latent membrane protein 1; LMP2A, Latent membrane protein 2A; MALT1, Mucosa-associated lymphoid tissue lymphoma translocation protein 1; MICA, MHC class I polypeptide-related sequence A; MICB, Major histocompatibility complex class I-related chain B; NDRG1, N-myc downstream-regulated gene 1; NLRP3, Nod-like receptor protein 3; TAP2, Transporter 2; PDL-1, Programmed cell death 1 ligand 1; PRDM1, PR domain zinc finger protein 1; PUMA, A p53 upregulated modulator of apoptosis.
This work was supported by the National Natural Science Foundations of China (81372139, 31670171), the Hunan Provincial Natural Science Foundation of China (2015JJ2149), and the Hunan Provincial Innovation Foundation for Postgraduates (CX2016B055).
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The authors declare that they have no conflict of interest. This article does not contain any studies with human or animal subjects performed by any of the authors.
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- . Adams BD, Kasinski AL, Slack FJ. 2014. Aberrant regulation and function of microRNAs in cancer. Curr Biol, 24: R762–R776.
- . Albanese M, Tagawa T, Bouvet M, Maliqi L, Lutter D, Hoser J, Hastreiter M, Hayes M, Sugden B, Martin L, Moosmann A, Hammerschmidt W. 2016. Epstein-Barr virus microRNAs reduce immune surveillance by virus-specific CD8+ T cells. Proc Natl Acad Sci U S A, 113: e6467–e6475.
- . Anastasiadou E, Boccellato F, Vincenti S, Rosato P, Bozzoni I, Frati L, Faggioni A, Presutti C, Trivedi P. 2010. Epstein-Barr virus encoded LMP1 downregulates TCL1 oncogene through miR-29b. Oncogene, 29: 1316–1328.
- . Barth S, Meister G, Grasser FA. 2011. EBV-encoded miRNAs. Biochim Biophys Acta, 1809: 631–640.
- . Barth S, Pfuhl T, Mamiani A, Ehses C, Roemer K, Kremmer E, Jaker C, Hock J, Meister G, Grasser FA. 2008. Epstein-Barr virus-encoded microRNA miR-BART2 down-regulates the viral DNA polymerase BALF5. Nucleic Acids Res, 36: 666–675.
- . Bazot Q, Paschos K, Skalska L, Kalchschmidt JS, Parker GA, Allday MJ. 2015. Epstein-Barr Virus Proteins EBNA3A and EBNA3C Together Induce Expression of the Oncogenic MicroRNA Cluster miR-221/miR-222 and Ablate Expression of Its Target p57KIP2. PLoS Pathog, 11: e1005031.
- . Becker A, Thakur BK, Weiss JM, Kim HS, Peinado H, Lyden D. 2016. Extracellular Vesicles in Cancer: Cell-to-Cell Mediators of Metastasis. Cancer Cell, 30: 836–848.
- . Bellot G., Cartron PF, Er E, Oliver L, Juin P, Armstrong LC, Bornstein P, Mihara K, Manon S, Vallette FM. 2007. TOM22, a core component of the mitochondria outer membrane protein translocation pore, is a mitochondrial receptor for the proapoptotic protein Bax. Cell Death Differ, 14: 785–794.
- . Bernhardt K, Haar J, Tsai MH, Poirey R, Feederle R, Delecluse HJ. 2016. A Viral microRNA Cluster Regulates the Expression of PTEN, p27 and of a bcl-2 Homolog. PLoS Pathog, 12: e1005405.
- . Bitar A, De R, Melgar S, Aung KM, Rahman A, Qadri F, Wai SN, Shirin T, Hammarstrom ML. 2017. Induction of immunomodulatory miR-146a and miR-155 in small intestinal epithelium of Vibrio cholerae infected patients at acute stage of cholera. PLoS One, 12: e0173817.
- . Buchan JR, Parker R. 2007. Molecular biology. The two faces of miRNA. Science, 318: 1877–1878.
- . Cai L, Ye Y, Jiang Q, Chen Y, Lyu X, Li J, Wang S, Liu T, Cai H, Yao K, Li JL, Li X. 2015. Epstein-Barr virus-encoded microRNA BART1 induces tumour metastasis by regulating PTEN-dependent pathways in nasopharyngeal carcinoma. Nat Commun, 2;6: 7353.
- . Ceccarelli S, Visco V, Raffa S, Wakisaka N, Pagano JS, Torrisi MR. 2007. Epstein-Barr virus latent membrane protein 1 promotes concentration in multivesicular bodies of fibroblast growth factor 2 and its release through exosomes. Int J Cancer, 121: 1494–1506.
- . Chen X, Shi J, Zhong J, Huang Z, Luo X, Huang Y, Feng S, Shao J, Liu D. 2015. miR-1, regulated by LMP1, suppresses tumour growth and metastasis by targeting K-ras in nasopharyngeal carcinoma. Int J Exp Pathol, 96: 427–432.
- . Chen YX, Man K, Ling GS, Chen Y, Sun BS, Cheng Q, Wong OH, Lo CK, Ng IO, Chan LC, Lau GK, Lin CL, Huang F, Huang FP. 2007. A crucial role for dendritic cell (DC) IL-10 in inhibiting successful DC-based immunotherapy: superior antitumor immunity against hepatocellular carcinoma evoked by DC devoid of IL-10. J Immunol, 179: 6009–6015.
- . Cho KJ, Song J, Oh Y, Lee JE. 2015. MicroRNA-Let-7a regulates the function of microglia in inflammation. Mol Cell Neurosci, 68: 167–176.
- . Choi H, Lee H, Kim SR, Gho YS, Lee SK. 2013. Epstein-Barr virus-encoded microRNA BART15-3p promotes cell apoptosis partially by targeting BRUCE. J Virol, 87: 8135–8144.
- . Chou J, Lin JH, Brenot A, Kim JW, Provot S, Werb Z. 2013. GATA3 suppresses metastasis and modulates the tumour microenvironment by regulating microRNA-29b expression. Nat Cell Biol, 15: 201–213.
- . Choy EY, Siu KL, Kok KH, Lung RW, Tsang CM, To KF, Kwong DL, Tsao SW, Jin DY. 2008. An Epstein-Barr virus-encoded microRNA targets PUMA to promote host cell survival. J Exp Med, 205: 2551–2560.
- . De Clercq E, Li G. 2016. Approved Antiviral Drugs over the Past 50 Years. Clin Microbiol Rev, 29: 695–747.
- . Diefenbach A, Jamieson AM, Liu SD, Shastri N, Raulet DH. 2000. Ligands for the murine NKG2D receptor: expression by tumor cells and activation of NK cells and macrophages. Nat Immunol, 1: 119–126.
- . Ding L, Li L, Yang J, Zhou S, Li W, Tang M, Shi Y, Yi W, Cao Y. 2007. Latent membrane protein 1 encoded by Epstein-Barr virus induces telomerase activity via p16INK4A/Rb/E2F1 and JNK signaling pathways. J Med Virol, 79: 1153–1163.
- . Dolken L, Malterer G, Erhard F, Kothe S, Friedel CC, Suffert G, Marcinowski L, Motsch N, Barth S, Beitzinger M, Lieber D, Bailer SM, Hoffmann R, Ruzsics Z, Kremmer E, Pfeffer S, Zimmer R, Koszinowski UH, Grasser F, Meister G, Haas J. 2010. Systematic analysis of viral and cellular microRNA targets in cells latently infected with human gamma-herpesviruses by RISC immunoprecipitation assay. Cell Host Microbe, 7: 324–334.
- . Du ZM, Hu LF, Wang HY, Yan LX, Zeng YX, Shao JY, Ernberg I. 2011. Upregulation of MiR-155 in nasopharyngeal carcinoma is partly driven by LMP1 and LMP2A and downregulates a negative prognostic marker JMJD1A. PLoS One, 6: e19137.
- . Due H, Svendsen P, Bødker JS, Schmitz A, Bøgsted M, Johnsen HE, El-Galaly TC, Roug AS, Dybkær KF. 2016. miR-155 as a Biomarker in B-Cell Malignancies. Biomed Res Int.
- . Dukers DF, Meij P, Vervoort MB, Vos W, Scheper RJ, Meijer CJ, Bloemena E, Middeldorp JM. 2000. Direct immunosuppressive effects of EBV-encoded latent membrane protein 1. J Immunol, 165: 663–670.
- . Fabbri M, Paone A, Calore F, Galli R, Gaudio E, Santhanam R, Lovat F, Fadda P, Mao C, Nuovo GJ., Zanesi N, Crawford M, Ozer GH, Wernicke D, Alder H, Caligiuri MA, Nana-Sinkam P, Perrotti D, Croce CM. 2012. MicroRNAs bind to toll-like receptors to induce prometastatic inflammatory response. Proc Natl Acad Sci USA, 109: E2110–E2116.
- . Forte E, Salinas RE, Chang C, Zhou T, Linnstaedt SD, Gottwein E, Jacobs C, Jima D, Li QJ, Dave SS, Luftig MA. 2012. The Epstein-Barr virus (EBV)-induced tumor suppressor microRNA MiR-34a is growth promoting in EBV-infected B cells. J Virol, 86: 6889–6898.
- . Gourzones C, Gelin A, Bombik I, Klibi J, Vérillaud B, Guigay J, Lang P, Témam S, Schneider V, Amiel C, Baconnais S, Jimenez AS, Busson P. 2010. Extra-cellular release and blood diffusion of BART viral micro-RNAs produced by EBV-infected nasopharyngeal carcinoma cells. Virol J, 7: 271.
- . Haar J, Contrant M, Bernhardt K, Feederle R, Diederichs S, Pfeffer S, Delecluse HJ. 2016. The expression of a viral microRNA is regulated by clustering to allow optimal B cell transformation. Nucleic Acids Res, 44: 1326–1341.
- . Haneklaus M, Gerlic M, Kurowska-Stolarska M, Rainey AA, Pich D, McInnes IB, Hammerschmidt W, O’Neill LA, Masters SL. 2012. Cutting edge: miR-223 and EBV miR-BART15 regulate the NLRP3 inflammasome and IL-1beta production. J Immunol, 189: 3795–3799.
- . Hooykaas MJG, van Gent M, Soppe JA, Kruse E, Boer IGJ, van Leenen D, Groot Koerkamp MJA, Holstege FCP, Ressing ME, Wiertz EJHJ, Lebbink RJ. 2017. EBV MicroRNA BART16 Suppresses Type I IFN Signaling. J Immunol, 198: 4062–4073.
- . Huang WT, Lin CW. 2014. EBV-encoded miR-BART20-5p and miR-BART8 inhibit the IFN-gamma-STAT1 pathway associated with disease progression in nasal NK-cell lymphoma. Am J Pathol, 184: 1185–1197.
- . Huye LE, Ning S, Kelliher M, Pagano JS. 2007. Interferon regulatory factor 7 is activated by a viral oncoprotein through RIP-dependent ubiquitination. Mol Cell Biol, 27: 2910–2918.
- . Iizasa H, Wulff BE, Alla NR, Maragkakis M, Megraw M, Hatzigeorgiou A, Iwakiri D, Takada K, Wiedmer A, Showe L, Lieberman P, Nishikura K. 2010. Editing of Epstein-Barr virus-encoded BART6 microRNAs controls their dicer targeting and consequently affects viral latency. J Biol Chem, 285: 33358–33370.
- . Jia S, Zhai H, Zhao M. 2014. MicroRNAs regulate immune system via multiple targets. Discov Med, 18: 237–247.
- . Jung YJ, Choi H, Kim H, Lee SK. 2014. MicroRNA miR-BART20-5p stabilizes Epstein-Barr virus latency by directly targeting BZLF1 and BRLF1. J Virol, 88: 9027–9037.
- . Kanda T, Miyata M, Kano M, Kondo S, Yoshizaki T, Iizasa H. 2015. Clustered microRNAs of the Epstein-Barr virus cooperatively downregulate an epithelial cell-specific metastasis suppressor. J Virol, 89: 2684–2697.
- . Kang BW, Choi Y, Kwon OK, Lee SS, Chung HY, Yu W, Bae HI, Seo AN, Kang H, Lee SK, Jeon SW, Hur K, Kim JG.. 2017. High level of viral microRNA-BART20-5p expression is associated with worse survival of patients with Epstein-Barr virus-associated gastric cancer. Oncotarget, 8: 14988–14994.
- . Kim DN, Lee SK. 2012. Biogenesis of Epstein-Barr virus microRNAs. Mol Cell Biochem, 365: 203–210.
- . Kim H, Choi H, Lee SK. 2015. Epstein-Barr virus miR-BART20-5p regulates cell proliferation and apoptosis by targeting BAD. Cancer Lett, 356: 733–742.
- . Komabayashi Y, Kishibe K, Nagato T, Ueda S, Takahara M, Harabuchi Y. 2014. Downregulation of miR-15a due to LMP1 promotes cell proliferation and predicts poor prognosis in nasal NK/T-cell lymphoma. Am J Hematol, 89: 25–33.
- . Li G, Wu Z, Peng Y, Liu X, Lu J, Wang L, Pan Q, He ML, Li XP. 2010a. MicroRNA-10b induced by Epstein-Barr virus-encoded latent membrane protein-1 promotes the metastasis of human nasopharyngeal carcinoma cells. Cancer Lett, 299: 29–36.
- . Li J, Fu R, Yang L, Tu W. 2015. miR-21 expression predicts prognosis in diffuse large B-cell lymphoma. Int J Clin Exp Pathol, 8: 15019–15024.
- . Li L, Chen XP, Li YJ. 2010b. MicroRNA-146a and human disease. Scand J Immunol, 71: 227–231.
- . Li L, Li Z, Zhou S, Xiao L, Guo L, Tao Y, Tang M, Shi Y, Li W, Yi W, Cao Y. 2007. Ubiquitination of MDM2 modulated by Epstein-Barr virus encoded latent membrane protein 1. Virus Res, 130: 275–280.
- . Li P, Liu C, Yu Z, Wu M. 2016. New Insights into Regulatory T Cells: Exosome- and Non-Coding RNA-Mediated Regulation of Homeostasis and Resident Treg Cells. Front Immunol, 7: 574.
- . Lisnic VJ, Krmpotic A, Jonjic S. 2010. Modulation of natural killer cell activity by viruses. Curr Opin Microbiol, 13: 530–539.
- . Liu X, Li L, Pan F, Tian W. 2012. MICB polymorphism in a southern Chinese Han population: the identification of two new MICB alleles, MICB*005:06 and MICB*026. Hum Immunol, 73: 818–823.
- . Liu X, Luo HN, Tian WD, Lu J, Li G1, Wang L, Zhang B, Liang BJ, Peng XH, Lin SX, Peng Y, Li XP. 2013. Diagnostic and prognostic value of plasma microRNA deregulation in nasopharyngeal carcinoma. Cancer Biol Ther, 14: 1133–1142.
- . Lo AK, To KF, Lo KW, Lung RW, Hui JW, Liao G, Hayward SD. 2007. Modulation of LMP1 protein expression by EBV- encoded microRNAs. Proc Natl Acad Sci U S A, 104: 16164–16169.
- . Lung RW, Tong JH, Sung YM, Leung PS, Ng DC, Chau SL, Chan AW, Ng EK, Lo KW, To KF. 2009. Modulation of LMP2A expression by a newly identified Epstein-Barr virus-encoded microRNA miR-BART22. Neoplasia, 11: 1174–1184.
- . Luo GG, Ou JH. 2015. Oncogenic viruses and cancer. Virol Sin, 30: 83–84.
- . Ma J, Nie K, Redmond D, Liu Y, Elemento O, Knowles DM, Tam W. 2016. EBV-miR-BHRF1-2 targets PRDM1/Blimp1: potential role in EBV lymphomagenesis. Leukemia, 30: 594–604.
- . Ma L, Deng X, Wu M, Zhang G, Huang J. 2014. Down-regulation of miRNA-204 by LMP-1 enhances CDC42 activity and facilitates invasion of EBV-associated nasopharyngeal carcinoma cells. FEBS Lett, 588: 1562–1570.
- . Mansouri S, Pan Q, Blencowe BJ, Claycomb JM, Frappier L. 2014. Epstein-Barr virus EBNA1 protein regulates viral latency through effects on let-7 microRNA and dicer. J Virol, 88: 11166–11177.
- . Marquitz AR, Mathur A, Nam CS, Raab-Traub N. 2011. The Epstein-Barr Virus BART microRNAs target the pro-apoptotic protein Bim. Virology, 412: 392–400.
- . Meckes DG, Jr., Shair KH, Marquitz AR, Kung CP, Edwards RH, Raab-Traub N. 2010. Human tumor virus utilizes exosomes for intercellular communication. Proc Natl Acad Sci U S A, 107: 20370–20375.
- . Miao BP, Zhang RS, Li M, Fu YT, Zhao M, Liu ZG, Yang PC. 2015. Nasopharyngeal cancer-derived microRNA-21 promotes immune suppressive B cells. Cell Mol Immunol, 12: 750–756.
- . Nachmani D, Stern-Ginossar N, Sarid R, Mandelboim O. 2009. Diverse herpesvirus microRNAs target the stress-induced immune ligand MICB to escape recognition by natural killer cells. Cell Host Microbe, 5: 376–385.
- . Onnis A, Navari M, Antonicelli G, Morettini F, Mannucci S, De Falco G, Vigorito E, Leoncini L. 2012. Epstein-Barr nuclear antigen 1 induces expression of the cellular microRNA hsa-miR-127 and impairing B-cell differentiation in EBV-infected memory B cells . New insights into the pathogenesis of Burkitt lymphoma. Blood Cancer J, 2: e84.
- . Oussaief L, Fendri A, Chane-Woon-Ming B, Poirey R, Delecluse HJ, Joab I, Pfeffer S. 2015. Modulation of MicroRNA Cluster miR-183-96-182 Expression by Epstein-Barr Virus Latent Membrane Protein 1. J Virol, 89: 12178–12188.
- . Patel SA, Gooderham NJ. 2015. IL6 Mediates Immune and Colorectal Cancer Cell Cross-talk via miR-21 and miR-29b. Mol Cancer Res, 13: 1502–1508.
Pegtel DM, Cosmopoulos K, Thorley-Lawson DA, van Eijndhoven MA, Hopmans ES, Lindenberg JL, de Gruijl TD, Wurdinger T, Middeldorp JM.
2010. Functional delivery of viral miRNAs via exosomes. Proc Natl Acad Sci U S A, 107: 6328–
- . Piedade D, Azevedo-Pereira JM. 2016. The Role of microRNAs in the Pathogenesis of Herpesvirus Infection. Viruses, 8.
- . Poole E, Sinclair J. 2015. Sleepless latency of human cytomegalovirus. Med Microbiol Immunol, 204: 421–429.
- . Qu JQ, Yi HM, Ye X, Zhu JF, Yi H, Li LN, Xiao T, Yuan L, Li JY, Wang YY, Feng J, He QY, Lu SS, Xiao ZQ. 2015. MiRNA-203 Reduces Nasopharyngeal Carcinoma Radioresistance by Targeting IL8/AKT Signaling. Mol Cancer Ther, 14: 2653–2664.
- . Ressing ME, van Gent M, Gram AM, Hooykaas MJ, Piersma SJ, Wiertz EJ. 2015. Immune Evasion by Epstein-Barr Virus. Curr Top Microbiol Immunol, 391: 355–381.
- . Riley KJ, Rabinowitz GS, Yario TA, Luna JM, Darnell RB, Steitz JA. 2012. EBV and human microRNAs co-target oncogenic and apoptotic viral and human genes during latency. EMBO J, 31: 2207–2221.
- . Rosato P, Anastasiadou E, Garg N, Lenze D, Boccellato F, Vincenti S, Severa M, Coccia EM, Bigi R, Cirone M, Ferretti E, Campese AF, Hummel M, Frati L, Presutti C, Faggioni A, Trivedi P. 2012. Differential regulation of miR-21 and miR-146a by Epstein-Barr virus-encoded EBNA2. Leukemia, 26: 2343–2352.
- . Saba R, Sorensen DL, Booth SA. 2014. MicroRNA-146a: A Dominant, Negative Regulator of the Innate Immune Response. Front Immunol, 5: 578.
- . Saki N, Abroun S, Soleimani M, Hajizamani S, Shahjahani M, Kast RE, Mortazavi Y. 2015. Involvement of MicroRNA in T-Cell Differentiation and Malignancy. Int J Hematol Oncol Stem Cell Res, 9: 33–49.
- . Sheedy FJ. 2015. Turning 21: Induction of miR-21 as a Key Switch in the Inflammatory Response. Front Immunol, 6: 19.
- . Skalsky RL, Kang D, Linnstaedt SD, Cullen BR. 2014. Evolutionary conservation of primate lymphocryptovirus microRNA targets. J Virol, 88: 1617–1635.
- . Song Y, Li X, Zeng Z, Li Q, Gong Z, Liao Q, Li X, Chen P, Xiang B, Zhang W, Xiong F, Zhou Y, Zhou M, Ma J, Li Y, Chen X, Li G, Xiong W. 2016. Epstein-Barr virus encoded miR-BART11 promotes inflammation-induced carcinogenesis by targeting FOXP1. Oncotarget, 7: 36783–36799.
- . Sun X, Zhang J, Hou Z, Han Q, Zhang C, Tian Z. 2015. miR-146a is directly regulated by STAT3 in human hepatocellular carcinoma cells and involved in anti-tumor immune suppression. Cell Cycle, 14: 243–252.
- . Sun Y, Cai J, Ma F, Lu P, Huang H, Zhou J. 2012. miR-155 mediates suppressive effect of progesterone on TLR3, TLR4-triggered immune response. Immunol Lett, 146: 25–30.
- . Tagawa T AM, Bouvet M, Moosmann A, Mautner J, Heissmeyer V, Zielinski C, Lutter D, Hoser J, Hastreiter M, Hayes M, Sugden B, Hammerschmidt W. 2016. Epstein-Barr viral miRNAs inhibit antiviral CD4+ T cell responses targeting IL-12 and peptide processing. J Exp Med, 213: 15.
- . Tang JF, Yu ZH, Liu T, Lin ZY, Wang YH, Yang LW, He HJ, Cao J, Huang HL, Liu G. 2014. Five miRNAs as novel diagnostic biomarker candidates for primary nasopharyngeal carcinoma. Asian Pac J Cancer Prev, 15: 7575–7581.
- . Tian T, Zhu YL, Zhou YY, Liang GF, Wang YY, Hu FH, Xiao ZD. 2014. Exosome uptake through clathrin-mediated endocytosis and macropinocytosis and mediating miR-21 delivery. J Biol Chem, 289: 22258–22267.
- . Tsang CM, Tsao SW. 2015. The role of Epstein-Barr virus infection in the pathogenesis of nasopharyngeal carcinoma. Virol Sin, 30: 107–121.
- . Verhoeven RJ, Tong S, Zhang G, Zong J, Chen Y, Jin DY. 2016. NF-kappaB Signaling Regulates Expression of Epstein-Barr Virus BART MicroRNAs and Long Noncoding RNAs in Nasopharyngeal Carcinoma. , 90: 6475–6488.
- . Wang Y, He D, Liang H, Yang D, Yue H, Zhang X, Wang R, Li B, Yang H, Liu Y, Chen Y, Duan Y, Zhang C, Chen X, Fu J. 2017. The identification of upregulated ebv-mir-BHRF1-2-5p targeting MALT1 and ebv-miR-BHRF1-3 in the circulation of patients with multiple sclerosis. Clin Exp Immunol, 2017 Jul;189: 120–126.
- . Xia T, O’Hara A, Araujo I, Barreto J, Carvalho E, Sapucaia JB, Ramos JC, Luz E, Pedroso C, Manrique M, Toomey NL, Brites C, Dittmer DP, Harrington WJ, Jr. 2008. EBV microRNAs in primary lymphomas and targeting of CXCL-11 by ebv-mir-BHRF1-3. Cancer Res, 68: 1436–1442.
- . Yan Q, Zeng Z, Gong Z, Zhang W, Li X, He B, Song Y, Li Q, Zeng Y, Liao Q, Chen P, Shi L, Fan S, Xiang B, Ma J, Zhou M, Li X, Yang J, Xiong W, Li G. 2015. EBV-miR-BART10-3p facilitates epithelial-mesenchymal transition and promotes metastasis of nasopharyngeal carcinoma by targeting BTRC. Oncotarget, 6: 41766–41782.
- . Yang F, Liu Q, Hu CM. 2015. Epstein-Barr virus-encoded LMP1 increases miR-155 expression, which promotes radioresistance of nasopharyngeal carcinoma via suppressing UBQLN1. Eur Rev Med Pharmacol Sci, 19: 4507–4515.
- . Yang GD, Huang TJ, Peng LX, Yang CF, Liu RY, Huang HB, Chu QQ, Yang HJ, Huang JL, Zhu ZY, Qian CN, Huang BJ. 2013. Epstein-Barr Virus_Encoded LMP1 upregulates microRNA-21 to promote the resistance of nasopharyngeal carcinoma cells to cisplatin-induced Apoptosis by suppressing PDCD4 and Fas-L. PLoS One, 8: e78355.
- . Yang IV, Wade CM, Kang HM, Alper S, Rutledge H, Lackford B, Eskin E, Daly MJ, Schwartz DA. 2009. Identification of novel genes that mediate innate immunity using inbred mice. Genetics, 183: 1535–1544.
- . Yang P, Li QJ, Feng Y, Zhang Y, Markowitz GJ, Ning S, Deng Y, Zhao J, Jiang S, Yuan Y, Wang HY, Cheng SQ, Xie D, Wang XF. 2012. TGF-beta-miR-34a-CCL22 signaling-induced Treg cell recruitment promotes venous metastases of HBV-positive hepatocellular carcinoma. Cancer Cell, 22: 291–303.
- . Yang Y, Wu BQ, Wang YH, Shi YF, Luo JM, Ba JH, Liu H, Zhang TT. 2016. Regulatory effects of miR-155 and miR-146a on repolarization and inflammatory cytokine secretion in human alveolar macrophages in vitro. Immunopharmacol Immunotoxicol: 1–27.
- . Yang Y, Zhou H, Li W, Zhou M, Zeng Z, Xiong W, Wu M, Huang H, Zhou Y, Peng C, Huang C, Li X, Li G. 2007. Lipopolysaccharide (LPS) regulates TLR4 signal transduction in nasopharynx epithelial cell line 5-8F via NFkappaB and MAPKs signaling pathways. Mol Immunol, 44: 984–992.
- . Yin W, Ouyang S, Li Y, Xiao B, Yang H. 2013. Immature dendritic cell-derived exosomes: a promise subcellular vaccine for autoimmunity. Inflammation, 36: 232–240.
- . Young LS, Rickinson AB. 2004. Epstein-Barr virus: 40 years on. Nat Rev Cancer, 4: 757–768.
- . Yu H, Lu J, Zuo L, Yan Q, Yu Z, Li X, Huang J, Zhao L, Tang H, Luo Z, Liao Q, Zeng Z, Zhang J, Li G. 2012. Epstein-Barr virus downregulates microRNA 203 through the oncoprotein latent membrane protein 1: a contribution to increased tumor incidence in epithelial cells. J Virol, 86: 3088–3099.
- . Yu P, Xiao L, Lin L, Tang L, Chen C, Wang F, Wang Y. 2016. STAT3-mediated TLR2/4 pathway upregulation in an IFN-gamma-induced Chlamydia trachomatis persistent infection model. Pathog Dis, 74.
- . Yu Z, Lu J, Yu H, Yan Q, Zuo L, Li G. 2011. A precise excision of the complete Epstein-Barr virus genome in a plasmid based on a bacterial artificial chromosome. J Virol Methods, 176: 103–107.
- . Zeng FR, Tang LJ, He Y, Garcia RC. 2015. An update on the role of miRNA-155 in pathogenic microbial infections. Microbes Infect, 17: 613–621.
- . Zeng L, Cui J, Wu H, Lu Q. 2014. The emerging role of circulating microRNAs as biomarkers in autoimmune diseases. Autoimmunity, 47: 419–429.
- . Zhang G, Zong J, Lin S, Verhoeven RJ, Tong S, Chen Y, Ji M, Cheng W, Tsao SW, Lung M, Pan J, Chen H. 2015. Circulating Epstein-Barr virus microRNAs miR-BART7 and miR-BART13 as biomarkers for nasopharyngeal carcinoma diagnosis and treatment. Int J Cancer, Mar 1;136(5): E301–E312.
- . Zhang J, Jia G, Liu Q, Hu J, Yan M, Yang B, Yang H, Zhou W, Li J. 2015a. Silencing miR-146a influences B cells and ameliorates experimental autoimmune myasthenia gravis. Immunology, 144: 56–67.
- . Zhang J, Li S, Li L, Li M, Guo C, Yao J, Mi S. 2015b. Exosome and exosomal microRNA: trafficking, sorting, and function. Genomics Proteomics Bioinformatics, 13: 17–24.
- . Zhao Y, Chen X, Jing M, Du H, Zeng Y. 2012. Expression of miRNA-146a in nasopharyngeal carcinoma is upregulated by Epstein-Barr virus latent membrane protein 1. Oncol Rep, 28: 1237–1242.
- . Zheng H, Li LL, Hu DS, Deng XY, Cao Y. 2007. Role of Epstein-Barr virus encoded latent membrane protein 1 in the carcinogenesis of nasopharyngeal carcinoma. Cell Mol Immunol, 4: 185–196.
- . Zheng XH, Lu LX, Cui C, Chen MY, Li XZ, Jia WH. 2016. Epstein-Barr virus mir-bart1-5p detection via nasopharyngeal brush sampling is effective for diagnosing nasopharyngeal carcinoma. Oncotarget, 7: 4972–4980.
- . Zhu H, Luo H, Li Y, Zhou Y, Jiang Y, Chai J, Xiao X, You Y, Zuo X. 2013. MicroRNA-21 in scleroderma fibrosis and its function in TGF-beta-regulated fibrosis-related genes expression. J Clin Immunol, 33: 1100–1109.