MALAT1, also referred to as nuclear-enriched abundant transcript 2, is a nuclear lincRNA >8,000 nt that is transcribed from chromosome 11q13 (26). The highly preserved level of MALAT1 in numerous species indicates its functional significance (25). MALAT1 has been shown to modulate primary transcripts transcriptionally or post-transcriptionally (27, 28).

Lai et al (29) reported that MALAT1 was increased in vitro and in vivo. In addition, analysis of multivariate data demonstrated that MALAT1 level was an independent prognostic factor for HCC recurrence. More importantly, the higher expression of MALAT1 was also associated with shortened patient disease-free survival following liver transplantation. These results suggest that treatment by targeting MALAT1 may be of clinical value by selectively eliminating diffuse or residual cancer cells following surgery. Silencing of MALAT1 by siRNA in HepG2 cells may significantly decrease cell viability, inhibit motility and invasiveness and sensitize cells to multi-stimuli-induced apoptosis.

Another lncRNA implicated in cancer metastasis is referred to as HOTAIR, is encoded in antisense direction from the HOXC gene cluster and acts in trans to regulate HOXD genes through interaction and recruitment of the polycomb repressive complex 2 (PRC2) to induce transcriptional silencing (30). Notably, pull-down assays with PRC2 revealed a direct and specific interaction with HOTAIR, which was an unexpected novel finding.

High levels of HOTAIR are mostly correlated with poor patient survival rate and tumor recurrence (31–33). Ishibashi et al (34) reported that high expression of HOTAIR was identified in primary HCCs in 13 of 64 patients. Patients with high HOTAIR expression exhibited significantly poorer prognoses and a larger primary tumor size compared to those with low HOTAIR expression. Furthermore, application of human HOTAIR to liver cancer cells demonstrated that HOTAIR induced a more rapid proliferation when compared to control samples.

Geng et al (35) demonstrated that knockdown of HOTAIR in the Bel7402 HCC cell line led to the reduction of matrix metalloproteinase-9 and vascular endothelial growth factor proteins, which are critical for cell motility and metastasis. Their study also revealed that there was a obvious association between HOTAIR level and lymph node metastasis. Thus, HOTAIR lincRNA may be a potential biomarker for the presence of lymph node metastasis in HCC. Yang et al (36) reported that the HOTAIR level in HCC was higher compared to that in adjacent non-cancerous tissues. Additionally, a high level of HOTAIR was an independent prognostic marker for predicting HCC recurrence in liver transplantation patients. Furthermore, patients with a higher level of HOTAIR exhibited significantly shorter recurrence-free survival. Similar to breast cancer, the inhibition of HOTAIR by siRNA in a liver cancer cell line decreased cell viability and invasion, sensitized cancer cells to tumor necrosis factor α-induced apoptosis and improved the sensitivity of cancer cells to cisplatin and doxorubicin.

Oncofetal H19 had been extensively investigated in cancer biology, even before research was focused on lncRNA (37, 38). H19 is a paternally imprinted gene which locates at chromosome 11p15.5. H19 is highly expressed during embryonic development, but is repressed right after birth in most tissues (39, 40). H19 is highly expressed during tumorigenesis and was shown to possess tumorigenic properties in all types of tissues (37, 41–43).

Matouk et al (44) demonstrated that H19 was excessively produced in a human HCC, even more than the traditional HCC marker α-fetoprotein. Therefore, an approach based on H19 knokdown may be an efficient method of targeting tumor cells. The results of that study suggested that HCC tumors transfected with H19 siRNA exhibited significant inhibition of tumor growth and, in certain cases, there was complete inhibition of tumor formation. There was a 82% decrease of mean tumor weights and mean tumor volumes in the two transfected cell lines. By contrast, Zhang et al (45) demonstrated that H19 was downregulated in intratumoral HCC tissues (T) when compared to peritumoral tissues (L). In addition, the Kaplan-Meier analysis revealed that HCC patients with low T/L ratios exhibited a worse prognosis compared to those with high ratios. H19 inhibited HCC metastasis and epithelial-to-mesenchymal transition. More importantly, H19 stimulated the miR-200 family by inducing histone acetylation, thus inhibiting the rate of tumor metastasis in advanced-stage HCC. The results of that study provided novel insights to the mechanism underlying the modulation of the level of small ncRNAs by lncRNAs. Yoshimizu et al (46) demonstrated that H19 regulated the timing of appearance of SV40-induced hepatocellular carcinoma using in vivo murine models of tumorigenesis. Therefore, it was concluded that H19 exerts a tumor suppressor effect in mice.

In summary, the above contradictory results indicate that the precise functions of H19 remain to be further investigated.

Another extensively investigated lncRNA is MEG3, which locates on chromosome 14q32. MEG3 belongs to the DLK1-MEG3 imprinting locus, containing at least three paternal protein-coding genes and abundant maternal ncRNAs (47, 48). The gene expression in this locus is firmly regulated by at least two differentially methylated regions (DMRs), namely the intergenic DMR and the MEG3-DMR (49).

MEG3 plays a crucial role in cell development and growth (50, 51). In humans, MEG3 is highly expressed in normal tissues and downregulation of MEG3 has been identified in a number of human tumors (50, 52). Additionally, upregulation of MEG3 inhibits in vitro tumor cell proliferation. Consequently, it was concluded that MEG3 is a tumor suppressor gene (53).

Braconi et al (54) reported that MEG3 was decreased by 210-fold in HCC tumor tissues compared to non-malignant hepatocytes. Enforced expression of MEG3 in HCC cells notably inhibited cell growth and increased apoptosis. Furthermore, hypermethylation of MEG3 promoter was detected by methylation-specific PCR and the level of MEG3 was increased with siRNA treatment of DNA methyltransferase (DNMT) 1 and 3b. More importantly, miR-29, which is able to regulate DNMT 1 and 3, increased the level of MEG3. These findings highlighted the interrelationship between two classes of non-coding RNAs, namely miRNAs and lncRNAs, and the epigenetic modulation of gene expression.

In addition, Anwar et al (55) suggested that the DLK1-MEG3 locus was continually deregulated in HCC. Knockdown of DNMT1 in HCC cells resulted in a reduction of MEG3-DMR methylation and a subsequent increase in the MEG3 level.

MVIH is located in the intron of the RPS24 gene and encodes a protein that belongs to the S24E family of ribosomal proteins (56). Despite the location of MVIH within the RPS24 gene, these two genes are transcribed separately, indicating that MVIH may play an independent role in biological behavior (57).

Yuan et al (58) reported an lncRNA termed MVIH that was increased in tumor tissues compared to the corresponding non-cancerous tissues and was associated with microvascular invasion of HCC. Furthermore, MVIH was considered to be an independent risk factor predictive of poor recurrence-free survival. The authors of that study also observed that MVIH was able to boost tumor growth and intrahepatic metastasis in vivo. The suppression of phosphoglycerate kinase 1 secretion by MVIH resulted in activation of angiogenesis in vitro and in vivo.

HULC is a~500-nt lncRNA located on chromosome 6p24.3 (59). Compared to non-neoplastic liver tissues, high expression of HULC was observed in HCC tissues (60). Xie et al (61) found that HULC lncRNA was detected with higher frequency in the plasma of HCC patients when compared to healthy controls. Higher HULC detection rates were also observed in the plasma of patients with higher Edmondson grades or with hepatitis B virus (HBV)-positive status. These findings suggested for the first time that the level of HULC in the plasma may be used as a novel, non-invasive biomarker for the diagnosis and/or prognosis of HCC. Interestingly, in other tumors, no obvious difference was observed in the expression of HULC between the tumor and normal tissues (62). In addition, high level of HULC was detected in metastatic liver nodules from colon cancer, but not in the primary colorectal carcinoma specimen and corresponding normal tissues. High level of HULC was also detected in liver metastases but not in lymph nodes, demonstrating its specificity to any malignant cells located in the liver (62).

Wang et al (63) provided evidence that HULC was a self-amplifying, auto-regulatory loop through inhibition of miRNA-372. There was a binding site of cAMP response element-binding protein (CREB) in the proximal promoter region of HULC (from −67 to −53 nt). Activation of the protein kinase A pathway was implicated in the upregulation of HULC. HULC may function as an endogenous ‘sponge’, downregulating the expression and activity of miR-372. Suppression of miR-372 resulted in reducing the translational inhibition of its target gene, cAMP-dependent protein kinase catalytic subunit beta, which in turn increased the phosphorylation of CREB. This regulatory loop demonstrates the latent interactions between lncRNAs and miRNAs and increases the complexity of the gene regulation network.

Liu et al (64) indicated that the variant genotypes of rs7763881 were significantly correlated with reduced HCC risk in a dominant genetic model. However, there was no significant association between single-nucleotide polymorphisms and HBV clearance. Therefore, the authors concluded that the variant genotypes of rs7763881 in HULC may contribute to the decreased susceptibility to HCC in HBV chronic carriers.

Du et al (65) revealed that HULC participated in HBx-mediated HCC. The expression of HULC was positively associated with the level of HBx in clinical HCC samples. Moreover, the luciferase reporter gene assay and chromatin immunoprecipitation assay indicated that HBx improved the activation of the HULC promoter via CREB. Finally, it was confirmed that the upregulation of HULC by HBx increased the proliferation of HCC cells through inhibiting p18. Taken together, these findings provide novel insight into the roles of lncRNAs in HBx-related HCC.

Recent studies revealed that several other lncRNAs are dysregulated in HCC. Huang et al (66) reported that downregulated expression by HBx (termed lncRNA-Dreh) was able to decrease HCC growth and function as a tumor suppressor in the progression of HBV-related HCC. It was further observed that lncRNA-Dreh altered the normal cytoskeleton structure to suppress tumor metastasis by targeting the intermediate filament protein vimentin. In addition, lncRNA-Dreh was significantly associated with poor prognosis of HCC. In summary, these results may provide a strategy for the development of lncRNA-based targeted methods for the treatment of HBV-related HCC. Yang et al (67) revealed that the level of lncRNA high expression in HCC (termed lncRNA-HEIH) in HBV-related HCC was markedly associated with recurrence and was an independent prognostic biomarker for survival. The authors of that study also manifested that lncRNA-HEIH played a pivotal role in G0/G1 arrest. It was further demonstrated that lncRNA-HEIH was correlated with enhancer of zeste homolog 2 (EZH2) and that this correlation was required for the inhibition of EZH2 target genes. Taken together, these results reveal that lncRNA-HEIH is an oncogenic lncRNA that promotes tumor development and, thus, it may act as a critical regulatory factor in HCC progression. Yang et al (68) indicated that uc002mbe.2 exhibited the most notable changes among these differentially expressed lncRNAs in HCC cell lines upon trichostatin A (TSA) treatment. Moreover, the TSA-induced uc002mbe.2 expression was positively associated with the apoptotic effect of TSA on HCC cells. Furthermore, a reduction in the level of uc002mbe.2 significantly decreased TSA-induced apoptosis of Huh7 cells, consequently unmasking that the TSA-induced apoptosis of HCC cells is uc002mbe.2-dependent and the low expression of uc002mbe.2 may be associated with liver carcinogenesis.