Lung cancer is the primary cause of cancer mortality and the most commonly occurring type of cancer worldwide (68,69). No fewer than 2.1 million people are diagnosed with lung cancer annually (1). Histologically, lung cancer can be divided into small cell lung cancer (SCLC) and NSCLC. Approximately 80–85% of newly diagnosed cases of lung cancer belong to the NSCLC type (70,71). Numerous lncRNAs, including HOXA11-AS, have been shown to have significant roles in NSCLC. Zhang et al (73,74) reported that the expression of HOXA11-AS is higher in both squamous cell carcinoma (SCC) and lung adenocarcinoma (LUAD) compared with that in normal lung tissues, and HOXA11-AS knockdown suppresses tumorigenesis, angiogenesis, proliferation, migration and invasion of NSCLC cells, inducing apoptosis by impeding the cell cycle at the G0/G1 or the G2/M phase. Moreover, Chen et al (75) identified that high levels of HOXA11-AS predict poor prognosis in patients with NSCLC. Furthermore, Yu et al (48) demonstrated that the expression level of HOXA11-AS is associated with lymph node metastasis and tumor size. Zhao et al (76) also reported that high levels of HOXA11-AS are associated with poor prognosis.

Mechanistically, Zhang et al (72–74) revealed that HOXA11-AS expression is negatively correlated with dedicator of cytokinesis 8 (DOCK8) in SCC and LUAD. Those authors conjectured that HOXA11-AS could have an oncogenic role in the development and progression of NSCLC by modulating various pathways, such as the transforming growth factor (TGF)-β pathway, the phosphoinositide 3-kinase (PI3K)-Akt pathway and the Hippo signaling pathway, and genes, such as DOCK8 gene. In other studies, the same authors demonstrated that the expression of HOXA11-AS co-expressed genes in NSCLC may be partly regulated by the NSCLC pathway and that HOXA11-AS could affect various biological processes of NSCLC via regulation of the expression of miR-642b-3p by targeting the expression of phosphodiesterase 4D (PDE4D) or other target genes (72–74). Additionally, Chen et al (75) found that HOXA11-AS interacts with DNA (cytosine-5)-methyltransferase 1 (DNMT1) and enhancer of zeste homolog 2 (EZH2), recruiting these proteins to the promoter regions of miR-200b and mediating methylation silencing of miR-200b in NSCLC cells, a process that promotes both NSCLC cell epithelial-mesenchymal transition (EMT) via regulation of the protein levels of E-cadherin, N-cadherin, Snail1/2 and ZEB1/2 and tumor progression. Yu et al (48) revealed that HOXA11-AS acts as a ceRNA to positively modulate the expression of transcription factor Sp1 by sequestering miR-124, a process that can inhibit cell proliferation and the invasion-promoting effects of HOXA11-AS. Futhermore, those authors found that HOXA11-AS can serve as an oncogene by promoting EMT via regulation of the protein levels of E-cadherin, β-catenin, vimentin and the EMT-mediating transcription factors Slug and Snail in NSCLC (48). Zhao et al (76) discovered that, in human LUAD cells, HOXA11-AS can function as a ceRNA to facilitate cisplatin tolerance through the miR-454-3p/Stat3 pathway (the abovementioned mechanisms are shown in Fig. 2A). Recent findings (77) have shown that membrane-bound extracellular vesicles, especially exosomes, serve significant roles as mediators for communication among different tissues and organs. Exosomes have a vital role in signal transduction among cells, and a wide range of biological functions. Wu et al (77) reported that high expression levels of HOXA11-AS in exosomes are closely associated with smoking and NSCLC in lung tissues. These findings indicate that HOXA11-AS has several functions associated with oncogenesis, regulating various physiological activities in NSCLC. These findings shed light upon the effects of HOXA11-AS on the progression of NSCLC and indicate that HOXA11-AS is a potential target for future treatment of NSCLC.

Hepatocellular carcinoma (HCC), which accounts for 90% of cases of liver cancer, is the fifth most frequent cancer in men and the ninth in women worldwide (78,79). The mortality rate of HCC ranks second in the world (80,81). Recently, cancer-associated studies focused on lncRNAs have demonstrated that a considerable number of lncRNAs are involved in the progression of HCC (82–84). Previous studies revealed that HOXA11-AS is overexpressed in HCC cells and tissues (82–84). Liu et al (82) found that high expression levels of HOXA11-AS are significantly correlated with vascular invasion, cirrhosis, tumor size and Edmondson grade. The overall survival (OS) rate of patients with high levels of HOXA11-AS expression is markedly shorter compared with those with lower levels of HOXA11-AS expression. Overexpression of HOXA11-AS promotes cell cycle progression, proliferation, invasion, and EMT, as well as repressing apoptosis in HCC cells.

Yu et al (83) reported that HOXA11-AS recruits PRC2 to the promoter region of large tumor suppressor 1 (LATS1) to obstruct its transcription, thereby promoting HCC growth and inhibiting apoptosis and cell cycle progression at the G0/G1 phase. The results from flow cytometry experiments indicated that the cell cycle progression of HCC cells was stalled at the G0/G1 phase when HOXA11-AS RNAi was transfected into HCC cells (83). Zhan et al (84) showed that the overexpression of HOXA11-AS is able to facilitate HCC proliferation and invasion, and induce EMT by repressing the expression of miR-214-3p. In addition, these authors demonstrated that the expression of miR-214-3p in early clinical stages (I–II) was higher than that in advanced clinical stages (III–IV). Furthermore, Liu et al (82) reported that HOXA11-AS recruits EZH2 to the promoter region of dual specificity protein phosphatase 5 (DUSP5), thereby inhibiting the transcription of DUSP5, which is a downstream target of HOXA11-AS and can function as a tumor suppressor gene. HOXA11-AS performs an oncogenic role in HCC by interacting with PRC2 (the abovementioned mechanisms are shown in Fig. 2B). HOXA11-AS may function as an oncogene in HCC development. The interaction between HOXA11-AS and LATS1, DUSP5 or miR-214-3p may supply novel prognostic markers and therapeutic targets for HCC.

Glioma, accounting for approximately 80% of primary malignant brain tumors, is the most aggressive primary tumor of the nervous system. Effective treatment of gliomas is very difficult, particularly glioblastomas (GBMs, also known as grade IV astrocytomas), with a median survival time for patients of less than 15 months using standard therapy (85–88). To date, although many studies have been focused on seeking improvements in diagnosis and treatment, the trend of poor prognosis has not been reversed (89). Among the numerous biomolecules involved in the occurrence and development of glioma, lncRNAs have attracted sustained attention due to their abnormal expression during tumorigenesis. Wang et al (90) discovered that high levels of HOXA11-AS expression are closely correlated with OS in high-grade glioma, and HOXA11-AS may be an independent prognostic factor for GBM. HOXA11-AS overexpression might occur during initial gliomagenesis and increased levels might be maintained in higher grades of gliomas. Those authors reported that the expression levels of HOTTIP, HOXA9, HOXA10, and HOXA13 are prominently correlated with HOXA11-AS expression, and HOXA11-AS can alter the expression of cell cycle-associated proteins, thus regulating cell cycle progression. Moreover, Cui et al (91) and Xu et al (92) found that high expression levels of HOXA11-AS are correlated with decreased survival time and poorer prognosis compared with patients with lower HOXA11-AS expression. In addition, Xu et al (93) found that the overexpression of HOXA11-AS is associated with advanced stages of glioma and poor prognosis. Authors of that study reported that knocking down the expression of HOXA11-AS leads to suppression of the proliferation, migration, and invasion rates of glioma cells in vitro, with the consequent further enhancement of cell cycle arrest at the G0/G1 stage and improved apoptotic responses.

Cui et al (91) showed that miR-140-5p is able to directly target the 3′-UTR of HOXA11-AS, and the effects of HOXA11-AS knockdown are shown to be reversed by an miR-140-5p inhibitor, as determined by its effects on cell cycle arrest, proliferation and apoptosis. Xu et al (92) demonstrated that HOXA11-AS functions as a ceRNA by sponging miR-214-3p, which can directly target EZH2 and suppress its mRNA transcriptional level. It was thereby confirmed that HOXA11-AS may serve in an oncogenic role by regulating the miR-214-3p/EZH2 pathway. Yang et al (94) found that HOXA11-AS leads to a marked increase in proliferation, invasion and migration rates, while inhibiting apoptosis by absorbing miR-124-3p in glioma cells. Furthermore, Xu et al (93) found that HOXA11-AS can exert its oncogenic role by directly binding to miR-130a-5p as a ceRNA, which inhibits the inhibitory effect of miR-130a-5p on HMGB2 expression. HMGB2 has been demonstrated to be involved in several diseases, such as sepsis, arthritis and cancer (the abovementioned mechanisms are shown in Fig. 2C). The above results suggest that HOXA11-AS may be an oncogene participating in the prognosis and treatment response of specific GBM subtypes.

Colorectal cancer (CRC) ranks third among the most common types of cancer in men, and second among women worldwide, with ~55% of CRC cases occurring in developed countries (95,96). The incidence of CRC has rapidly increased in China, and in 2011, it was shown to be the second most common cause of cancer-associated mortality (97). Although recent advances have been made in the diagnosis and treatment of CRC in recent years, the prognosis of patients diagnosed with CRC remains poor; in fact, the 5-year survival rate in patients with metastatic CRC has been shown to be less than 20% (98,99). Li et al (100) reported that HOXA11-AS is downregulated in CRC cell lines and tissues, and low expression levels of HOXA11-AS are associated with advanced tumor-lymph node-metastasis (TNM) stages, lymphatic metastasis, large tumor size and elevated levels of carcinoembryonic antigen (CEA). Authors of that study also showed that the lncRNA HOXA11-AS may distinguish CRC tissue from noncancerous tissue, and they further explored the correlation between HOXA11-AS and lymph node metastasis. Moreover, Chen et al (101) reported that the level of HOXA11-AS was markedly upregulated in CRC patients with liver metastasis, and the migration and invasion of CRC cells was facilitated by HOXA11-AS. In addition, Chen et al (101) found that HOXA11-AS can act as a ceRNA sequestering miR-125a-5p to modulate the expression of protein-arginine deiminase type-2 (PADI2), which was shown to facilitate metastasis and the invasion of CRC (the abovementioned mechanisms are shown in Fig. 2D). Consequently, a novel HOXA11-AS/miR-125a-5p/PADI2 pathway, involved in CRC liver metastasis, was identified. Taken together, these results demonstrated that HOXA11-AS is a potential biomarker and molecular therapy target in CRC.

Breast cancer (BC) is one of the most frequent causes of cancer-associated mortality in women worldwide (102,103). Although great progress has been made in earlier diagnosis of this disease and in the effective of systemic therapies, the overall prognosis of BC remains unsatisfactory. In particular, distant metastasis is a barrier for successful treatment (104–106). Su and Hu (107) discovered that lncRNA HOXA11-AS is overexpressed in human BC, and the expression of HOXA11-AS is markedly associated with metastasis, tumor size and TNM staging. Clinical statistics revealed that the expression of HOXA11-AS was correlated with Ki-67 protein and human epidermal growth factor receptor (HER2), but not with estrogen receptor (ER) or progesterone receptor (PR). Their results indicated that decreased expression levels of HOXA11-AS in human BC led to suppression in the rates of cell proliferation, migration and invasion, and cell cycle arrest at the G0/G1 phase. Li et al (108) also reported that low levels of HOXA11-AS expression inhibited cell proliferation and induced tumor cell apoptosis by inducing cell cycle arrest at the G0/G1 stage. By contrast, high levels of HOXA11-AS expression facilitated metastasis and invasion both in vitro and in vivo by exerting an influence on EMT in BC (the abovementioned mechanisms are shown in Fig. 2E). Note that the above articles (107,108) only determined the involvement of HOXA11-AS in these processes; the specific mechanisms have yet to be properly elucidated. These studies, however, have confirmed that HOXA11-AS exerts carcinogenic effects in BC, thereby providing some novel insights for even earlier diagnosis in the future, and for the therapy of BC.

Gastric cancer. Gastric cancer (GC) ranks the fifth among the most common types of cancer, and is the third leading cause of cancer mortality (109). GC is more common in men: The mortality rate in men is 2-fold higher compared with women (1). In men, GC is the most commonly occurring gastrointestinal malignancy in East Asia, the most common cancer in several Western Asian countries and the main cause of cancer deaths (110,111). Despite advances in surgical techniques and the successful development of targeted drugs, the 5-year OS rate, however, remains unsatisfactory, and the majority of patients are diagnosed with advanced cancer along with lymphatic metastasis (98). Sun et al (112) reported that HOXA11-AS is significantly upregulated in GC tissues. High levels of HOXA11-AS expression are closely related to poor differentiation, larger tumor size, lymph node metastasis and advanced pathological stage in GC. Researchers also found that progression-free survival (PFS) and OS rates in excess of 3 years in the group with high levels of HOXA11-AS expression were lower compared with the group with low levels of HOXA11-AS expression. HOXA11-AS overexpression leads to increased rates of cell growth, migration and invasion, and inhibition of apoptosis in GC. By contrast, Liu et al (113) reported that HOXA11-AS knockdown induces G0/G1 phase arrest in GC cells and decreases GC cell metastasis, migration and invasion, both in vitro and in vivo.

In terms of the underlying mechanism, Sun et al (112) demonstrated that HOXA11-AS acts as a protein scaffold to recruit EZH2, accompanied by DNMT1 or LSD1. In addition, HOXA11-AS functions as a miR-1297 sponge, thereby regulating the translation of EZHZ, a direct miR-1297 target. Knockdown of HOXA11-AS increases the expression of the tumor suppressors, serine protease 8 (PRSS8) and Krüppel-like Factor 2 (KLF2), leading to the promotion of cell proliferation and invasion and inhibiting apoptosis in GC cells. Those authors reported that EZH2 can directly bind to the promoter regions of PRSS8 and KLF2 and DNMT1 can directly bind to the promoter region of KLF2 to stimulate H3K27me3 modifications. LSD1 is also able to directly bind to the promoter region of PRSS8 to mediate H3K4 demethylation. Knockdown of HOXA11-AS suppresses the binding capability of DNA with several chromatin modification factors (namely, PRC2, LSD1 and DNMT1). Moreover, Sun et al (112) identified the potential regulator E2F1, which can directly bind to the promoter region of HOXA11-AS and regulate the transcription of HOXA11-AS. In addition, HOXA11-AS can function as an oncogene by regulating the miR-1297/EZH2 and HOXA11-AS-EZH2/DNMT1/LSD1-KLF2/PRSS8 pathways to promote GC cell proliferation, migration and invasion and inhibit apoptosis. Liu et al (113) identified that HOXA11-AS enhances β-catenin transcription by interacting with WD repeat-containing protein 5 (WDR5), and p21 transcription is subsequently inhibited via binding with EZH2. In addition, HOXA11-AS can interact with double-stranded RNA-binding protein staufen homolog 1 (STAU1) to promote KLF2 mRNA degradation. These findings revealed that HOXA11-AS may serve as an oncogene by modulating the HOXA11-AS-WDR5/EZH2/STAU1-β-catenin/p21/KLF2 pathway (Fig. 3A). Taken together, these results have revealed that HOXA11-AS can function as an oncogene in GC cells, further elucidating the role of HOXA11-AS in promoting better diagnosis of the disease, and developing further how lncRNA may be used in treatments of GC.

Clear cell renal cell carcinoma (ccRCC) is a common malignant tumor of the urinary system, accounting for >80% of all types of RC (114). No fewer than 209,000 new cases of ccRCC are reported each year, and among these cases, approximately 25–30% of the patients present with distant metastasis and 40% of patients have local recurrence after the initial diagnosis (115,116). The biological behavior of ccRCC is extremely complex and the underlying molecular mechanisms have yet to be fully elucidated, factors which explain how prognosis is both poor and difficult to predict (117). Recently, Yang et al (118) found that HOXA11-AS was clearly upregulated in ccRCC cell lines and tissues, and high HOXA11-AS expression levels were very closely correlated with lymph node metastasis, tumor stage and advanced clinical stage. Downregulation of the HOXA11-AS transcript led to a marked decrease in the growth, proliferation, invasion, and EMT of the ccRCC cells. Regarding the mechanism, Yang et al (118) discovered that HOXA11-AS functions as a ceRNA to suppress the expression of miR-146b-5p, which subsequently modulates the expression of its downstream target, matrix metalloproteinase-16 (MMP16) in RC. Therefore, HOXA11-AS promotes RC cell invasion and proliferation by regulating the miR-146b-5p/MMP16 pathway (Fig. 3B). During this process, HOXA11-AS may function as an oncogene in ccRCC and may therefore represent an efficient therapeutic target for RCC.

Uveal melanoma. Uveal melanoma (UM) ranks first among primary intraocular malignant tumors in adults, and the uvea ranks second among the common sites of primary melanoma (119,120). The metastatic rate of UM is very high, and UM ultimately spreads to the liver in up to 50% of patients (121). Lu et al (122) discovered that HOXA11-AS is overexpressed in UM, and HOXA11-AS is shown to enhance the rates of UM cell proliferation and invasion, while repressing apoptosis. Authors of that study also reported that HOXA11-AS recruits EZH2 to the promoter region of p21 and mediates H3K27me3 to suppress its transcription. Furthermore, HOXA11-AS acts as a ceRNA for miR-124, which directly targets EZH2, and the cell proliferation and invasion-increasing effects of HOXA11-AS were attenuated upon miR-124 overexpression (Fig. 3C). Taken together, these studies indicate that HOXA11-AS has an oncogenic role through regulating the HOXA11-AS/EZH2/p21 and miR-124/EZH2 pathways in UM tumorigenesis, and HOXA11-AS may also represent a potential therapeutic target for treatment of UM.

Ovarian malignancies are among the most commonly occurring malignancies in female reproductive organs. The most frequent ovarian malignancy type is cutaneous carcinoma, followed by malignant germ cell tumor. Among these malignant gynecological tumors, the mortality rate of epithelial ovarian cancer (EOC) is the highest, posing a serious threat to women's health (1). A large number of studies have shown that not only HOXA11-AS, but also many other lncRNAs act as oncogenes or tumor suppressor genes in different cancers. Ignarski et al (123) reported that the expression pattern of lncRNA genes is far more tissue- and cell-type specific than is the case for protein coding genes. HOXA11-AS exerts opposing effects in different types of cancer. Such expressional and functional discrepancies of HOXA11-AS in different types of cancer could be caused by distinct gene expression backgrounds in different tumors (124). For example, in EOC, HOXA11-AS can act as a tumor suppressor gene, which is different from the tumor mentioned above.

It has been reported that common germline genetic variants or single nucleotide polymorphisms (SNPs) affecting lncRNAs are conducive to the development of various types of cancer (125), such as EOC (126). Richards et al (126) reported that overexpression of HOXA11-AS results in a clear reduction in cell proliferation and survival, which are two main cellular processes associated with EOC development in both common and minor allele constructs. In particular, the existence of minor allele constructs markedly reduced the proliferation and survival of EOC cells compared with the common allele, and the expression of both alleles served to diminish cell migration and invasion. However, compared with the common allele, the minor allele exerted a more pronounced suppressive effect in both assays. Richards et al (126) found that the minor allele repressed the carcinogenic phenotypes to a greater extent compared with the common allele in EOC cells. The finding has identified a greatly decreased risk of EOC among women who have the HOXA11-AS rs17427875 T allele (126). In EOC tumor tissue, HOXA11-AS expression was reduced by over 60% on average compared with normal ovarian tissue. Richards et al (126) also found HOXA11-AS cannot exert any influence upon HOXA11 and HOXA13 (Fig. 3D). Thus, these studies suggest that HOXA11-AS may function as a tumor suppressor gene in EOC.

Laryngeal squamous cell carcinoma (LSCC) is a commonly occurring malignant tumor of the upper respiratory tract. Laryngeal carcinoma is ranked second in terms of the most frequently occurring malignant tumors in the head and neck (127). Qu et al (128) found that the expression levels of HOXA11-AS are closely correlated with pathological grade, T (tumor) grade, clinical stage, neck nodal metastasis and advanced tumors of grade T3 to T4 in LSCC. Furthermore, advanced clinical stages, poor prognosis, poor differentiation and lymph node metastasis were identified in patients who expressed higher levels of HOXA11-AS. Authors of that study also found that HOXA11-AS was able to promote LSCC cell proliferation, invasion and migration (Fig. 3E). Notably, only the general effects attributable to HOXA11-AS were identified in the study of Qu et al (128), and the specific mechanism involved requires further investigation. However, their results have demonstrated that HOXA11-AS may function as an oncogene, suggesting that it is a potential novel biomarker and an efficient therapeutic target in LSCC.

It is estimated that CC is the fourth leading cause of cancer mortality, and ranks fourth out of the most commonly diagnosed cancers among women. In 2018, there were approximately 570,000 CC cases and 311,000 cancer-associated deaths worldwide (1). In fact, in terms of its incidence and the mortality rates, CC is ranked second behind BC (1). Kim et al (129) reported that the expression of HOXA11-AS is specifically upregulated in CC, and OS and 5-year survival rates are both reduced in CC patients with HOXA11-AS overexpression. Cox multivariate proportional hazards analysis revealed that nodal metastasis, tumor stage, and HOXA11-AS are independent prognosticators of OS. Those authors found that HOXA11-AS is associated with enhanced cell proliferation, also leading to increased rates of cell migration and invasion in CC. In terms of the underlying mechanism, HOXA11-AS promotes CC cell migration and invasion by upregulating the levels of MMP-9, MMP-2, and vascular endothelial growth factor (VEGF), and disordering of the EMT-associated genes suggested that HOXA11-AS may be involved in cell migration and invasion in CC (Fig. 3F). Kim et al (129) also showed that HOXA11-AS can promote activation of the genetic program that supports the cancer stem cell (CSC) phenotype and improves EMT, suggesting that HOXA11-AS may function as an oncogene in CC. Thus, HOXA11-AS may be a therapeutic target in the search for improved treatments for CC.

Among the different types of cancer, ESCC is ranked seventh in terms of its incidence and sixth in terms of overall mortality, which means that 1 out of every 20 cases of cancer-associated mortality in 2018 was estimated to have been caused by ESCC (1). Sun et al (130) found that high expression levels of HOXA11-AS are correlated with lymph node metastasis and histological grade in patients with ESCC. Compared with those patients with HOXA11-AS overexpression, patients with low HOXA11-AS expression exhibited both increased median disease-free survival (DFS) and median OS. Sun et al (130) found that lymph node metastasis and the expression of HOXA11-AS were independent poor prognosis factors in patients with ESCC (Fig. 3G). Taking all these findings into consideration, HOXA11-AS may have an oncogenic role in ESCC, and therefore HOXA11-AS may also represent a predictive marker in postoperative ESCC patients.

Osteosarcoma is ranked the first among the most commonly occurring types of primary malignant bone cancer, and is placed second in terms of cancer-associated deaths in pediatrics (131). lncRNAs are well known to be involved in the development of most tumors. Cui et al (60) found that a high level of HOXA11-AS expression is correlated with distant metastasis, reduced OS and advanced clinical stage in patients with osteosarcoma. Their study suggested that HOXA11-AS knockdown in osteosarcoma induces cell cycle arrest at the G0/G1 phase, and HOXA11-AS overexpression led to a substantial improvement in cell invasion and growth rates in osteosarcoma cells via the competitive binding of miR-124-3p, which targets Rho-associated, coiled-coil-containing protein kinase 1 (ROCK1) (Fig. 3H). In this manner, HOXA11-AS may exert oncogenic functions by regulating the miR-124-3p/ROCK1 pathway. Investigating the underlying mechanistic roles of the HOXA11-AS/miR-124-3p/ROCK1 pathway may be an important step in developing novel osteosarcoma therapeutic strategies.

Given the ever-increasing aging population, fractures have become a serious health problem, constituting the most common injuries sustained worldwide. Despite the body being capable of healing fractures, many risk factors have substantially delaying effects on the process of fracture healing, including advanced age, smoking, diabetes mellitus (DM) and anti-cancer drugs (132). Therefore, it is imperative to explore the mechanisms underlying fracture healing, notably in patients with these factors, is an urgent requirement. Numerous studies have been published that demonstrate how lncRNAs are able to participate in the occurrence and development of many diseases, including fracture healing (133). Wang et al (133) found that HOXA11-AS overexpression led to a suppression of OS-732 osteoblast proliferation and improved apoptosis. In addition, HOXA11-AS can act as a ceRNA by sequestering miR-124-3p to inhibit cell proliferation and enhance apoptosis (Fig. 3I). These results may provide a novel perspective for deciphering the mechanism of fracture healing.

Preeclampsia (PE) is the leading cause of pregnancy-associated death and fetal defects (134). PE is characterized as having a blood pressure exceeding 140/90 mmHg from the 20th week of pregnancy onwards. Between 3 and 5% of pregnant women experience PE, especially in developing countries (135). Xu et al (136) found that HOXA11-AS expression was markedly downregulated in pre-eclamptic placental tissues, and reducing HOXA11-AS expression led to a clear inhibition of trophoblast cell growth and migration. Mechanistically, those authors revealed that HOXA11-AS recruits LSD1 and EZH2 proteins to the RND3 gene promoter region in the nucleus to repress its expression in trophoblast cells. When the level of HOXA11-AS expression was reduced in trophoblast cells, its ability to bind to LSD1 and EZH2 was also reduced, leading to decreased LSD1 and EZH2 binding to the RND3 gene promoter region and decreasing the inhibitory effect on RND3, which suppresses cell growth and proliferation. Furthermore, HOXA11-AS facilitated the expression of HOXA7 in the cytoplasm via sequestration of miR-15b-5p, thus exerting an influence on trophoblast proliferation (Fig. 3J). These studies revealed that HOXA11-AS may have an oncogenic function via modulating the LSD1/EZH2-RND3 and HOXA11-AS/miR-15b-5p/HOXA7 pathways. Consequently, these results have verified that abnormal expression of HOXA11-AS is involved in the occurrence and development of PE, and that this lncRNA may function as a putative target for diagnosis and treatment in PE.

With rapid economic development and aging of the population, the number of patients with DM is increasing annually. Persistent hyperglycemia induces hyperglycemia-associated complications that pose severe medical risks, such as diabetic arteriosclerosis (DAA), atherosclerosis (AS) and cardiomyopathy (137). Studies have revealed that the incidence of cardio-cerebrovascular diseases in DM patients is markedly higher than in non-DM patients. In view of the role of lncRNAs in a variety of different tumor types and diseases, researchers have also examined the role of lncRNA in diabetes. Jin et al (138) found that expression levels of HOXA11-AS and pro-inflammatory genes were substantially increased in carotid endarterectomy specimens of DM patients, and HOXA11-AS expression was also significantly increased in the carotid arteries of DM mice. Mechanistically, HOXA11-AS knockdown reduces the expression of proliferation-associated gene (PCNA), the cell cycle-related genes p21 and p53, and platelet-derived growth factor (PDGF)-induced growth and migration of vascular smooth muscle cells (VSMCs) is repressed, significantly downregulating the expression of inflammation-associated genes in VSMCs induced by tumor necrosis factor-α (TNF-α). Moreover, in vascular endothelial cells (VECs), low expression levels of HOXA11-AS were shown to suppress the expression of TNF-α-induced pro-inflammatory genes and PDGF-induced vascular inflammation-related genes. Low expression levels of HOXA11-AS inhibited the PDGF-induced stimulation of the PI3K/AKT pathway by inhibiting the phosphorylation of PI3K and AKT in VSMCs and VECs (Fig. 3K). The biological functions of HOXA11-AS in DAA-induced inflammation should be further explored to identify potential new effective treatments for DAA.