Insights into the roles of lncRNAs in skeletal and dental diseases

Long noncoding RNAs (lncRNAs) are a class of non-protein-coding transcripts with the length longer than 200 nucleotides. Growing evidence suggests that lncRNAs, which were initially thought to be merely transcriptional “noise”, participate in a wide repertoire of biological processes. It has been well established that lncRNAs not only play important roles in genomic regulation, transcription, posttranscriptional processes but are also implicated in the pathogenesis of human diseases including cardiovascular diseases, diabetes, neurodegenerative disorders, and cancer. However, the pathological role of lncRNAs in skeletal and dental diseases is just beginning to be uncovered. In the present review, we outline the current understanding of the established functions and underlying mechanisms of lncRNAs in various cellular processes. Furthermore, we discuss new findings on the role of lncRNAs in osteoblastogenesis and osteoclastogenesis as well as their involvement in skeletal and dental diseases. This review intends to provide a general framework for the actions of lncRNAs and highlight the emerging evidence for the functions of lncRNAs in skeletal and dental diseases.

The term noncoding RNA (ncRNA) refers to diverse RNA molecules that do not encode any protein. ncRNAs include infrastructural RNAs such as transfer RNAs (tRNAs), ribosomal RNAs (rRNAs), small nuclear RNAs (snRNAs), and small nucleolar RNAs (snoRNAs) [1]. Increasing evidence indicates that additional regulatory ncRNAs such as lncRNAs exist and play important roles in regulating chromatin architecture/epigenetic memory, transcription, and mRNA splicing, stability, and translation [2].

lncRNAs are among the least understood RNAs despite their pervasive transcription in the genome. The most updated annotation of the human genome (Version 27, GRCh38) identifies 27,908 lncRNA transcripts from 15,778 lncRNA genes (http://www.gencodegenes.org/stats/current.html). Like mRNAs, many polyadenylated lncRNAs are transcribed by RNA polymerase II (Pol II) and are often alternatively spliced into multiple isoforms. But genes coding for lncRNAs also have characteristics distinct from those for mRNAs: lncRNA genes have fewer but longer exons, tend to be expressed at lower levels, and exhibit less-conserved sequences [3]. However, some lncRNAs that are expressed in development- and tissue-specific patterns have highly conserved promoter regions and splice sites [4].

lncRNAs do not possess any apparent protein-coding potential and are mostly expressed at low levels; they are thus characterized largely by bioinformatic approaches. Advances in high-throughput RNA sequencing technologies provide systems with which RNA transcription can be observed in an unbiased manner [5]. lncRNAs have been shown to regulate various biological processes via distinct mechanisms [6], whereas mutations or aberrant expression of lncRNAs have been implicated in the pathogenesis of a wide range of human diseases [7,8,9].

In this review, we briefly present the current knowledge of the functions and mechanisms of lncRNAs. We then review the role of lncRNAs in osteoblastogenesis and osteoclastogenesis based on data from multiple studies. Finally, we discuss the important roles of lncRNAs in the etiology of skeletal and dental disorders.

The discovery of the myriad roles of lncRNAs has made it increasingly clear that lncRNAs can function via numerous paradigms and are key regulatory molecules in cells [6]. They not only participate in nuclear events such as chromatin modification and transcription [10], but also reside in the cytoplasm, where they interact with RNA-binding proteins or modulate mRNA translation. Here, we outline a concise scheme of the functions of lncRNAs for a better understanding of what roles lncRNAs play in osteoblastogenesis, osteoclastogenesis, as well as skeletal and dental diseases.

lncRNAs in chromatin modification

In the nucleus, lncRNAs target some chromatin remodeling complexes and guide them to specific genomic loci, leading to changes in gene transcription. A classic example is a long intergenic noncoding RNA (lincRNA) termed X inactive-specific transcript (XIST), which is transcribed from one of the two X chromosomes in female mammals (Fig. 1a). It recruits polycomb group complexes, such as polycomb repressive complex 2 (PRC2) [11], to the female X chromosome, leading to transcriptional silencing in cis across a majority of the chromosome. In contrast, lncRNA HOTAIR, which is transcribed from the antisense strand of homeobox C (HOXC) locus, recruits PRC2 in trans to the HOXD cluster for epigenetic repression [12].

Schematic representation of how lncRNAs may function in genome regulation. a The participation of lncRNA XIST in chromosome silencing. XIST recruits PRC2 to the female X chromosome, leading to H3K27me3 formation (presented as pink pentagon with “Me”) and silencing of the chromosome. b Chromatin modification by lncRNA HOTTIP. HOTTIP interacts with adaptor protein WDR5 and targets WDR5/MLL complexes, inducing H3K4me3 (presented as a pink pentagon with “Me”) and transcription of 5′HOXA genes. c Evf-2 as an example of lncRNAs that facilitate transcriptional activation. Combination of Evf-2 with the protein Dlx-2 forms an Evf-2/Dlx-2 complex, which targets the Dlx-5/6 enhancer region and promotes transcription. Question marks indicate that the specific role of Evf-2 in the process remains to be elucidated. d Alu ncRNA can act as a potent transcriptional repressor. Alu RNA contains RNA polymerase II (Pol II, enzyme that synthesizes mRNAs in eukaryotes) binding arms and modular repression domains, allowing it to bind Pol II and block RNA synthesis

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lncRNAs also associate with other chromatin regulators. An example is the lineage-specific imprinting mediated by the lncRNA Kcnq1ot1, a nuclear and moderately stable transcript from the paternal chromosome. In addition to interacting with members of the PRC2 complex, Kcnq1ot1 also recruits chromatin regulators such as G9a methyltransferase to mediate repressive histone modifications, including the trimethylation of lysine 27 on histone H3 (H3K27me3) and trimethylation of lysine 9 on histone H3 (H3K9me3) in the Kcnq1 domain [13].

However, some lncRNAs function in chromatin activation rather than chromatin silencing. Enhancers are regulatory elements that increase the expression of target genes [14]. An enhancer-like lncRNA termed HOTTIP has been identified as a key intermediate that transmits information from higher order chromosomal looping into chromatin modifications. HOTTIP is transcribed from the distal 5′tip of the HOXA locus and is brought into close proximity to multiple HOXA genes by chromosomal looping of the HOXA 5′end. It directly binds the adaptor protein WDR5 and targets WDR5/MLL complexes across the HOXA locus, leading to histone H3 lysine 4 trimethylation (H3K4me3) and gene transcription [15] (Fig. 1b).

lncRNAs in transcription regulation

As shown above, lncRNAs indirectly influence transcription through chromatin modification. However, some lncRNAs regulate transcription directly. The 3.8-kb lncRNA Evf-2 is transcribed from the Dlx-5/6 ultraconserved region. Evf-2 has been found to activate the transcriptional activity of the Dlx-5/6 enhancer by cooperating with a homeodomain protein Dlx-2 (Fig. 1c). This single-stranded RNA and the ultraconserved protein form an Evf-2/Dlx-2 complex and then the complex targets the Dlx-5/6 enhancer. But whether the complex helps Dlx-2 bind to the enhancer site or only helps stabilize the protein requires further investigation [16]. Nevertheless, some lncRNAs serve as transcriptional repressors [6]. In response to heat shock, the Alu ncRNA binds Pol II and enters complexes at promoters, ultimately blocking all detectable RNA synthesis (Fig. 1d). An interesting thing is that although there are sequence discrepancies between the Pol II-binding domains of Alu RNA and B2 RNA (Alu RNA-like sequences in mouse), both of them repress transcription by Pol II. So the mechanism by which Alu RNA functions may not be sequence specific [17].

lncRNAs in pre-mRNA splicing

In the nucleus, lncRNAs are implicated in posttranscriptional regulatory steps, including pre-mRNA splicing, mRNA capping, polyadenylation, and nuclear export. Pre-mRNA splicing is a key process to increase proteome diversity in higher eukaryotes [18]. The lncRNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) has been proposed to regulate alternative splicing (AS) by modulating the distribution of active serine/arginine-rich (SR) proteins in nuclear speckle domains. SR proteins are essential splicing factors that function in both constitutive splicing and AS [19, 20]. Previous studies indicated that MALAT1 modulated AS of endogenous pre-mRNAs by regulating SR splicing factors phosphorylation, as well as altering the distribution and ratio of phosphorylated versus non-phosphorylated pools of SR proteins (Fig. 2a). These changes may lead to alterations in the expression of specific isoforms of proteins in cells [21].

A schematic diagram illustrating the involvement of lncRNAs in posttranscriptional processes. a lncRNA MALAT1 is implicated in pre-mRNA splicing. MALAT1 changes the expression and ratio of phosphorylated (orange circle with the letter “p”) versus dephosphorylated serine/arginine-rich (SR) proteins (splicing factors can regulate splicing; blue circle), thus altering the splicing mode of pre-mRNAs. b lncRNAs also influence mRNA stability. lncRNA BACE1-AS associates with cell stressor Aβ 1–42 and stabilizes BACE1 mRNA (dashed line represents unstable mRNA). c lncRNAs may cause mRNA decay. lncRNA 1/2-sbsRNA mediates mRNA decay by binding protein STAU1, with further base-pairing with an Alu element at the 3′-untranslated regions (3′-UTRs) of CDCP1 or MTAP mRNA (dashed line represents unstable mRNA). lncRNAs can serve as activators d or repressors e in mRNA translation. Antisense Uchl1 RNA associates mRNA with active polysomes, resulting in the promotion of translation. Conversely, lincRNA-p21 enhances interaction between translational repressor Rck and mRNAs such as CTNNB1 and JUNB, giving rise to polysome size reduction and translation repression. f lncRNAs also act as miRNA sponges, leading to derepression of miRNA targets. As indicated, lncRNA linc-MD1 “sponges” miR-133 and miR-135, antagonizing the miRNA-mediated translation suppression

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Another example of involvement of lncRNA in AS is sno-lncRNA, a class of nuclear-enriched intron-derived lncRNAs transcribed from a critical region of chromosome 15 (15q11-q13). This region is specifically deleted in Prader–Willi Syndrome (PWS). sno-lncRNAs are flanked by snoRNA sequences at both ends [22]. Studies have demonstrated that at least some of these sno-lncRNAs acted as molecular sinks of the splicing regulator Fox2, a member of the Fox family. sno-lncRNAs binded to Fox2 and altered the splicing patterns. Importantly, sno-lncRNA knockdown leaded to changes in Fox2-regulated splicing, while the overall gene expression levels were unaltered [23].

lncRNAs in mRNA protection and decay

As an intermediate, mRNA carries information from genes to ribosomes for protein synthesis. However, it is unstable and the concentration of mRNA depends on the balance between the rates of synthesis and degradation [24]. lncRNAs are increasingly recognized as important modulators of both mRNA synthesis and degradation.

Functional characterization of the lncRNA BACE1-AS has revealed the action of lncRNAs in maintaining mRNA stability. BACE1-AS is a conserved antisense transcript partner of β-site amyloid precursor protein cleaving enzyme 1 (BACE1), which is a crucial enzyme in the pathogenesis of Alzheimer’s disease. When exposured to amyloid-β 1–42 (Aβ 1–42), which can induce oxidative stress, elevated BACE1-AS levels increase BACE1 mRNA stability and generate additional Aβ 1–42 through a posttranscriptional feed-forward mechanism [25] (Fig. 2b).

Another type of lncRNA exerts its function by facilitating mRNA decay. Staufen 1 (STAU1) is a double-stranded RNA binding protein that binds to a subset of mRNAs and targets them for STAU1-mediated mRNA decay (SMD) [26]. Half-STAU1-binding site RNA (1/2-sbsRNA) is a polyadenylated lncRNA that induces mRNA decay by recruiting STAU1 to target mRNAs. STAU1-binding sites can be formed by imperfect base-pairing between an Alu element of an mRNA target of SMD and another Alu element in 1/2-sbsRNAs. The 1/2-sbsRNA-regulated mRNAs such as CUB-domain-containing protein 1 (CDCP1) mRNA and methylthioadenosine phosphorylase (MTAP) mRNAs can thus be degraded [27] (Fig. 2c).

lncRNAs in translation activation and repression

mRNA translation is the final step of protein synthesis. Recent studies have demonstrated that some lncRNAs control protein synthesis by either post-transcriptional activation or repression of mRNA translation in the cytoplasm.

The nuclear-enriched lncRNA, antisense Uchl1, forms sense-antisense pairs by pairing with the ubiquitin carboxy-terminal hydrolase L1 (Uchl1) gene. Under stress conditions, antisense Uchl1 lncRNA shuttles from the nucleus to the cytoplasm. It then binds the 5′end of the Uchl1 mRNA and promotes the association of this overlapping sense protein-coding mRNA with active polysomes for translation [28] (Fig. 2d).

On the contrary, lincRNA-p21 inhibits the translation of target mRNAs encoding β-catenin (CTNNB1) and JunB (JUNB) after HuR (also known as embryonic lethal abnormal vision 1, ELAVL1) is silenced. HuR is a ubiquitous RNA-binding protein that functions in cell proliferation, survival, and carcinogenesis, as well as in stress and immune responses [29, 30]. HuR exerts its functions mainly by interacting with a subset of mRNAs, and further increasing their stability and modulating their translation [31]. HuR also enhances the decay of lincRNA-p21. Therefore, in the absence of HuR, stable lincRNA-p21 inhibits the translation of CTNNB1 and JUNB mRNAs by enhancing their interaction with the translational repressor Rck, which may result in polysome size reduction and even ribosome “drop-off” [32] (Fig. 2e).

lncRNAs in miRNA biology

microRNAs (miRNAs) are endogenous 19–23-nucleotide RNAs that negatively regulate gene expression at the post-transcriptional level. They interact with partially complementary sequences in the 3′-UTR of a target mRNA, leading to translational repression, mRNA cleavage, and mRNA decay [33, 34]. Recent reports have demonstrated that lncRNAs may prevent the repressive effects of miRNAs on their targets [35,36,37]. lncRNAs function as competing endogenous RNAs (ceRNAs) to sequester miRNAs, thereby protecting the target mRNAs from degradation [38].

linc-MD1 has been implicated as a ceRNA that competes for shared miRNAs with mRNAs. Therefore, it can be regarded as an activator in mRNA translation. Linc-MD1 “sponges” miR-133 and miR-135 to regulate the mRNA translation of mastermind-like-1 (MAML1) and myocyte-specific enhancer factor 2C (MEF2C), respectively (Fig. 2f). With the finding that both MAML1 and MEF2C are critical genes for normal myogenic differentiation [39], linc-MD1 is postulated to be involved in the control of myoblast differentiation [40]. The well-known lncRNA H19 has been identified as a novel activator of the Wnt/β-catenin pathway by serving as a miRNA sponge. H19 antagonizes the functions of miR-141 and miR-22, both of which are negative modulators of the Wnt/β-catenin pathway and osteogenesis. The presence of H19 leads to the derepression of their shared target gene, β-catenin, and eventually promotes osteoblast differentiation [41].

Mesenchymal stem cells (MSCs) have the potential to differentiate into multiple cell types, including osteoblasts, chondrocytes, adipocytes, and neurocytes [42]. Osteoclasts are derived from hematopoietic precursor cells of the monocyte-macrophage lineage. They are large, multinucleated, terminally differentiated cells, functioning as the sole bone-resorbing cells [43]. Skeletal development and adult bone remodeling depend on the coordinated function of osteoblasts and osteoclasts, which differentiate from precursor cells in the mesenchymal osteoblastic lineage [44] and the hematopoietic osteoclastic lineage [45], respectively.

The involvement of lncRNAs in the differentiation of MSCs into osteoblasts has been unveiled over the past decade (Table 1). Analysis of lncRNA expression profiles has revealed significant differences between untreated and bone morphogenetic protein 2 (BMP-2)-treated C3H10T1/2 MSCs [46]. In the study, the authors used BMP-2 to induce early osteoblastogenesis, and compared the differential expression profiles of lncRNA by microarray and bioinformatic approaches. Over 100 differentially expressed lncRNAs were identified. A subset of 24 lncRNAs was determined to concurrently change with their nearby coding genes, which are involved in osteoblastogenesis. For example, mouselincRNA0231 and its nearby gene epidermal growth factor receptor (EGFR), which suppressed osteoblast differentiation via regulating Runx2 and Osterix, were downregulated after BMP-2 treatment. A similar correlation was observed between NR_027652 and mouselincRNA0243 with their respective nearby coding genes DLK1 and IL-5, respectively. Another study demonstrated that anti-differentiation ncRNA (ANCR) regulated Runx2 expression and osteoblastogenesis. ANCR interacted with the enhancer of zeste homolog 2 (EZH2). The recruitment of ANCR with EZH2 catalyzed H3K27me3 in Runx2 gene promoter, resulting in the inhibition of Runx2 expression and subsequent osteoblastogenesis [47].

The function of the lncRNA hypoxia-inducible factor 1α-anti-sense 1 (HIF1α-AS1) in osteoblastogenesis was recently identified. HIF1α-AS1 expression was significantly repressed after overexpression of the histone deacetylase sirtuin 1 (SIRT1), an important regulator of osteoblast differentiation [48]. Lower levels of SIRT1 gave rise to the upregulation of HIF1α-AS1 in human bone marrow stem cells (BMSCs). Moreover, HIF1α-AS1 knockout inhibited the expression of HOXD10 by interfering with acetylation, suggesting the potential role of HIF1α-AS1 in the activation of osteoblastogenesis [49].

Attention has also been paid to the effects of lncRNAs on dentinogenesis (Table 1). Dentinogenesis shares many similarities with osteogenesis, and consists of multiple steps including odontoblast differentiation. Chen et al. showed that lncRNAs were involved in the odontoblast-like differentiation of human dental pulp cells (hDPCs) [50]. In their study, the expression of the differentiation-antagonizing lncRNA DANCR was considerably downregulated in a time-dependent manner in the process of hDPCs differentiation into odontoblast-like cells. Furthermore, mineralized nodule formation as well as the expression of dentin sialophosphoprotein and dentin matrix protein-1 was blocked after overexpression of DANCR in hDPCs. Upregulation of DANCR also decreased the expression levels of p-GSK-3β and β-catenin. These results reveal a role of DANCR in regulating the Wnt/β-catenin pathway and modulating dentin formation.

lncRNAs also play a regulatory role in osteoclastogenesis (Table 1). In one study, microarray analysis was performed to examine the expression profiles of lncRNAs at different stages of osteoclastogenesis. Then gene ontology analysis, pathway analysis, and lncRNA-mRNA co-expression network characterization showed the co-expression of multiple lncRNAs with tumor necrosis factor ligand superfamily member (TNFSF)12 and TNFSF13 [51], factors involved in the differentiation of monocyte/macrophage precursor cells into osteoclasts [52, 53]. Circulating monocytes are directly involved in osteoclastogenesis by acting as osteoclast precursors [54]. The role of lncRNA DANCR in blood mononuclear cells has been studied. Overexpression of DANCR increased the secretion of IL-6 and TNF-α in blood mononuclear cells [55], both of which were inflammatory cytokines and important mediators of accelerated bone loss in osteoporosis [56, 57]. This suggests that DANCR can be a potential biomarker and regulatory element in circulating monocytes for osteoclastogenesis. However, further studies are needed to determine the underlying mechanisms of lncRNAs in osteoclastogenesis.

lncRNAs not only play critical roles in various aspects of cellular biology but are also implicated in disease pathogenesis and progression. Several lncRNAs have been functionally associated with important pathogenic processes of cardiovascular diseases [58], diabetes [59], neurodegenerative disorders [60], immune response [61], as well as several types of cancer [62, 63]. However, the identity of lncRNAs in skeletal and dental diseases is not well known. Here, we summarize new findings in the functions of lncRNAs in these diseases (Table 1).

Osteoporosis

Emerging evidence demonstrates the correlation of lncRNAs with osteoporosis, which is a common metabolic bone disorder [55]. Osteoporosis is characterized by reduced bone mineral density and increased incidence of fractures, resulting mainly from enhanced osteoclastic bone resorption activity outpacing bone formation by osteoblasts [64]. The sequence encoding lncRNA DANCR resides on human chromosome 4, located 54.8 kb upstream of USP46 and 28.7 kb downstream from ERVMER34-1 and the ANCR locus. As mentioned above, DANCR was upregulated in circulating monocytes of postmenopausal women with low bone mineral density, and could induce the expression of IL-6 and TNF-α [55]. These results suggest the important role of DANCR in the pathogenesis of osteoporosis and possibly as a biomarker for postmenopausal osteoporosis (PMOP). Another case is the involvement of lncRNA MEG3 in the pathogenesis of PMOP [65]. In this study, MEG3 expression was increased in BMSCs derived from PMOP patients and ovariectomized mice. MEG3 directly bound to and activated miR-133a-3p, thereby inhibiting the expression of SLC39A1 (a direct target of miR-133a-3p), which was regarded as a positive regulator of osteogenic differentiation. Overexpression of MEG3 inhibited osteogenic differentiation of BMSCs, which was markedly reversed by miR-133a-3p knockdown. These data indicate that lncRNAs participate in the pathogenesis of osteoporosis, which provide novel targets for the prevention and treatment of osteoporosis.

Skeletal transformation

After its first identification in primary human fibroblasts [66], the lncRNA Hotair has also been found to be important in the embryonic patterning of the skeletal system [67]. Targeted deletion of Hotair resulted in lumbosacral homeotic transformation (6th lumbar vertebrae transform to 1th sacral vertebrae, L6 → S1) in a C57BL/6 mouse model. Moreover, malformation of the metacarpals and 4th caudal vertebrae was also observed. Hotair knockdown caused derepression of multiple HoxD cluster genes in embryos and tail tip fibroblasts. Insights into the molecular basis for the observed phenotypes revealed that Hotair acted in trans to bind both PRC2 and LSD1 complex. Hotair recruited them to hundreds of genomic sites to promote coordinated H3K27 methylation and H3K4 demethylation for gene silencing. However, in another study, the skeletal malformation indicated above was not detected after Hotair knockdown in a mixed CBAxBL/6 mouse model [68]. Whether the discrepancy in the phenotypic effects of Hotair knockdown is attributed to the different genetic background of animals needs further study.

Osteoarthritis

Osteoarthritis (OA) is the clinical and pathological outcome of a range of disorders that results in structural and functional failure of synovial joints. While many risk factors (e.g., IL-1, IL-6, TNF-α, PGE2, MMPs) contribute to the onset of OA [69], the mechanism responsible for OA has not been fully elucidated. Recent studies have investigated the effects of lncRNAs on OA. Xing et al. reported that over 100 lncRNAs were up- or down-regulated in OA cartilage compared with normal cartilage based on microarray analysis. The increased expression of six lncRNAs (HOTAIR, GAS5, PMS2L2, RP11-445H22.4, H19 and CTD-2574D22.4) in the microarray data was validated by real-time PCR [70], suggesting the regulatory potential of lncRNAs in OA. SOX9nc2 is a cartilage-specific lncRNA which lies upstream of SOX9 in the genome. Depletion of the SOX9nc2 transcript by RNA interference prevented chondrogenesis and the expression of the transcription factor SOX9 [71]. Moreover, a significant correlation has been observed among the expression of lncRNA H19, miR-675, and COL2A1 in OA cartilage. Co-upregulation of H19, COL2A1, and miRNA-675 was observed in chondrocytes under hypoxic conditions, which were known to stimulate chondrocyte anabolism. When chondrocytes were treated with inflammatory factors IL-1β and TNF-α to induce chondrocyte catabolism, the expression of H19, COL2A1, and miRNA-675 was significantly decreased [72]. In addition, Dudek et al. showed that inhibition of H19 downregulated COL2A1, while overexpression of miR-675 rescued COL2A1 expression in H19-depleted human articular chondrocytes [73]. More work is needed to investigate the function and mechanisms of lncRNAs as key regulators of OA.

Periodontitis

Evidence for the relationship between periodontitis and lncRNAs is emerging. Periodontitis is a common chronic inflammatory disease initiated by a group of bacterial pathogens in dental plaque. The inflammation extends deep into tissues, damages the connective tissue and alveolar bone around teeth, and eventually leads to tooth loss [74]. Microarray analysis of lncRNA expression profile revealed a total of 8925 differently expressed lncRNAs in chronic periodontitis tissues compared with adjacent normal tissues. Further subgroup analysis showed there were 589 enhancer-like lncRNAs, 238 HOX cluster lncRNAs, as well as 1218 lincRNAs. Based on the information, the function and mechanisms of lncRNAs associated with periodontitis needs further investigation [75]. The role of a crucial lncRNA related to periodontitis, lncRNA-POIR, has recently been investigated. lncRNA-POIR expression was significantly lower in periodontal mesenchymal stem cells (PDLSCs) from periodontitis patients (pPDLSCs) than that in human periodontal MSCs (hPDLSCs). Overexpression of lncRNA-POIR promoted osteogenic differentiation of pPDLSCs. Further study revealed that lncRNA-POIR acted as a ceRNA for miR-182, thus positively regulating expression of FoxO1. The inflammatory environment, which usually occurred in periodontitis, increased miR-182 expression through NF-κB pathway, finally resulted in an imbalance in the lncRNA-POIR-miR-182 regulatory network [76]. The association between periodontitis and another lncRNA ANRIL has also been reported. ANRIL is the first shared genetic risk factor of coronary artery disease and aggressive periodontitis [77]. Bochenek et al. demonstrated that ANRIL knockdown resulted in repression of three genes ADIPOR1, VAMP3, and C11ORF10. Exploration of the identified genes highlighted a region upstream of VAMP3 within CAMTA1 (rs10864294) to be associated with increased risk of coronary artery disease and aggressive periodontitis [78]. These studies indicate the potential of lncRNAs as diagnostic biomarkers and targets for the treatment of periodontitis.

Osteosarcoma

Differences in the expression of lncRNAs in different types of tumors have been well documented [79, 80]. This finding promoted interest in addressing the potential of lncRNAs in skeletal tumors. Osteosarcoma is the most common primary malignant tumor of bone with cytogenetic complexity. The lncRNA TUSC7 (tumor suppressor candidate 7), previously named as LOC285194, was significantly downregulated in osteosarcomas. The decreased expression of TUSC7 was due to copy number loss of the genomic region on chr3q13.31. Depletion of TUSC7 promoted proliferation and inhibited apoptosis in osteosarcoma cells. TUSC7 suppression also increased osteosarcoma growth in a mouse model, and was correlated with poor survival of osteosarcoma patients [81, 82]. In addition, recent studies revealed that the lncRNA MALAT1 was dysregulated in multiple malignant tumors, including osteosarcoma. Knockdown of MALAT1 decreased proliferation, migration, and induced apoptosis in osteosarcoma. MALAT1 knockdown significantly inhibited PI3K/AKT and RhoA/ROCK signaling pathway. High expression of MALAT1 was closely correlated with pulmonary metastasis in patients with osteosarcoma [83, 84]. Interestingly, Fang et al. demonstrated that downregulation of MALAT1 induced by high dose of 17β-Estradiol promoted the binding of SFPQ to oncogene PTBP2, therefore affecting proliferation, migration or invasion in osteosarcoma cells [85]. Further discussion of lncRNAs in osteosarcoma can be found elsewhere [86, 87].

Ameloblastoma

Ameloblastoma is a benign but locally invasive odontogenic tumor of the jaws [88]. It often results in facial deformity and significant morbidity because of its high rate of recurrence and requirement for radical surgery. Considerable efforts have been made to clarify the underlying molecular mechanisms and actions of lncRNAs in ameloblastoma. The ncRNA expression profile of ameloblastoma was characterized in a well-defined ameloblastoma cohort. In this study, whole transcriptome profiling by microarray followed by real-time PCR assays validated five highly associated ncRNAs, including the lncRNA LINC340 (also known as CASC15). However, whether LINC340 is a prognostic and therapeutic marker that can improve the treatment of ameloblastoma requires further investigation [89].

Over the past decade, extensive research has established that lncRNAs play important roles in diverse cellular processes. Moreover, the molecular mechanisms by which lncRNAs exert their functions have been largely elucidated. These discoveries have promoted investigators in the skeletal and dental fields to address the potential role of lncRNAs in regulating the differentiation and function of bone cells as well as in the pathogenesis of skeletal and dental diseases. However, whereas a few studies have revealed the functional role of some lncRNAs, most of the results have merely demonstrated an association of lncRNAs with either bone cell biology or the development of some skeletal and dental diseases. Hence, future investigations should focus on further establishing the functional links between lncRNAs and hard tissue diseases and elucidating the underlying molecular mechanisms. A better understanding of the regulatory roles and molecular mechanisms of lncRNAs in skeletal and dental diseases may identify new biomarkers for diagnosis and novel therapeutic targets for these disorders.

ANCR:

anti-differentiation noncoding RNA

AS:

alternative splicing

Aβ 1-42:

amyloid-β 1-42

BACE1:

β-secretase-1

BMSC:

bone marrow stem cell

BMP-2:

bone morphogenetic protein 2

CDCP1:

CUB-domain-containing protein 1

ceRNA:

competing endogenous RNA

DANCR:

differentiation-antagonizing long noncoding RNA

EGFR:

epidermal growth factor receptor

EZH2:

enhancer of zeste homolog 2

hDPC:

human dental pulp cell

HIF1α-AS1:

hypoxia-inducible factor 1α-anti-sense 1

HOX:

homeobox

hPDLSC:

human periodontal mesenchymal stem cell

H3K4me3:

trimethylation of lysine 4 on histone H3

H3K9me3:

trimethylation of lysine 9 on histone H3

H3K27me3:

trimethylation of lysine 27 on histone H3

lincRNA:

long intergenic noncoding RNA

lncRNA:

long noncoding RNA

LSD1:

lysine-specific demethylase 1

MALAT1:

metastasis-associated lung adenocarcinoma transcript 1

MAML1:

mastermind-like-1

MEF2C:

myocyte-specific enhancer factor 2C

miRNA:

microRNA

MSC:

mesenchymal stem cell

MTAP:

methylthioadenosine phosphorylase

ncRNA:

non-protein-coding RNA

OA:

osteoarthritis

PDLSC:

periodontal mesenchymal stem cell

PMOP:

postmenopausal osteoporosis

Pol II:

polymerase II

pPDLSC:

patient periodontal mesenchymal stem cell

PRC2:

polycomb repressive complex 2

PWS:

Prader–Willi Syndrome

rRNA:

ribosomal RNA

RT-PCR:

real-time polymerase chain reaction

SIRT1:

sirtuin 1

SMD:

STAU1-mediated mRNA decay

snoRNA:

small nucleolar RNA

snRNA:

small nuclear RNA

SR protein:

serine/arginine-rich protein

STAU1:

Staufen 1

TNFSF:

necrosis factor ligand superfamily

tRNA:

transfer RNA

Uchl1:

ubiquitin carboxy-terminal hydrolase L1

XIST:

X inactive-specific transcript

1/2-sbsRNA:

half-STAU-1-binding site RNA

3′-UTR:

3′-untranslated region

YL wrote the manuscript. JZ, JP and PD created the figures. XY, YX and YW made the table and revised the manuscript. XF and SZ revised and approved this manuscript prior to its submission. All authors read and approved the final manuscript.

Acknowledgements

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Not applicable.

Funding

This work was supported by the National Natural Science Foundation of China [Grant Number: 81470777].

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Affiliations

1. State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, No.14, 3rd Section, Renmin South Road, Chengdu, 610041, China
   • Yuyu Li
   • , Jiawei Zhang
   • , Jie Pan
   • , Peipei Duan
   • , Xing Yin
   • , Yang Xu
   • , Xin Wang
   •  & Shujuan Zou
2. Department of Orthodontics, West China Hospital of Stomatology, Sichuan University, No.14, 3rd Section, Renmin South Road, Chengdu, 610041, China
   • Yuyu Li
   • , Jiawei Zhang
   • , Jie Pan
   • , Peipei Duan
   • , Xing Yin
   • , Yang Xu
   • , Xin Wang
   •  & Shujuan Zou
3. Department of Pathology, University of Alabama at Birmingham, 1670 University Blvd., VH G019E, Birmingham, AL, 35294, USA
   • Xu Feng

Corresponding author

Correspondence to Shujuan Zou.

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