LncRNAs HNF1α-AS1/HNF4α-AS1 in Drug Metabolism and Human Diseases: History
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Subjects: Pharmacology & Pharmacy
Contributor:
Xiao-bo Zhong

Long noncoding RNAs (lncRNAs) are RNAs with a length of over 200 nucleotides that do not have protein-coding abilities. Recent studies suggest that lncRNAs are highly involved in physiological functions and diseases. lncRNAs HNF1α-AS1 and HNF4α-AS1 are transcripts of lncRNA genes HNF1α-AS1 and HNF4α-AS1, which are antisense lncRNA genes located in the neighborhood regions of the transcription factor (TF) genes HNF1α and HNF4α, respectively. HNF1α-AS1 and HNF4α-AS1 have been reported to be involved in several important functions in human physiological activities and diseases. In the liver, HNF1α-AS1 and HNF4α-AS1 regulate the expression and function of several drug-metabolizing cytochrome P450 (P450) enzymes, which also further impact P450-mediated drug metabolism and drug toxicity. In addition, HNF1α-AS1 and HNF4α-AS1 also play important roles in the tumorigenesis, progression, invasion, and treatment outcome of several cancers. Through interacting with different molecules, including miRNAs and proteins, HNF1α-AS1 and HNF4α-AS1 can regulate their target genes in several different mechanisms including miRNA sponge, decoy, or scaffold.

  • lncRNA
  • HNF1α-AS1
  • HNF4α-AS1
  • cancer
  • cytochrome P450

1. Introduction

The advancement of next-generation sequencing techniques makes it possible to investigate the human genome in a clearer and more detailed aspect. In addition to the coding genes, the noncoding genes, which actually take up the majority of the human genome, have also been investigated [1]. The transcripts of noncoding genes are defined as noncoding RNAs (ncRNAs). Initially, ncRNAs were believed to have no protein coding function as they do not have protein-coding open-reading frames (ORFs). However, this idea was challenged by several recent findings, showing that some ncRNAs can generate microproteins/small peptides, which gave rise to a new insight into the ncRNA functions [2][3]. Along with the progress in the identification of all kinds of ncRNAs, the studies focusing on the functions and mechanisms of ncRNAs are also boosting.
Long ncRNAs (lncRNAs) are a group of ncRNAs with more than 200 nt in length [4]. lncRNAs are found to be highly involved in the regulation of gene expression and functions. This feature of lncRNAs makes them also important for many biological and physiological processes in human and other organisms. Up to date, several lncRNA databases have been established to assist the study of lncRNAs, including the GENCODE, LNCipedia, ENCODE, and NONCODE [5][6][7][8]. According to the GENCODE database, 17,960 lncRNAs have been annotation in the human genome in 2020 [5]. However, compared to the large number of annotated lncRNAs, far fewer lncRNAs have been functionally characterized and understood. A huge knowledge gap remains in understanding how lncRNAs can impact on human health.
Hepatocyte nuclear factor 1 alpha-antisense-1 (HNF1α-AS1) and HNF4α-antisense-1 (HNF4α-AS1) are two recently identified lncRNAs in human. They are named based on their genomic locations, where the noncoding genes HNF1α-AS1 and HNF4α-AS1 are located next to two important transcription factor (TF) genes HNF1α and HNF4α and are transcribed in the opposite direction on the antisense strand. Several special functions and mechanisms of these two lncRNAs have been found in normal physiologic activities and abnormal diseases.

2. Neighborhood Antisense lncRNAs HNF1α-AS1 and HNF4α-AS1

2.1. Classification of lncRNAs Based on Genomic Locations

lncRNA genes can be found in several different locations relative to coding genes in the genomes (Figure 1) [9]. Intergenic lncRNAs (lincRNAs) are lncRNAs located between two coding genes. Intronic lncRNAs are lncRNAs positioned within the intronic region of a coding gene. Sense lncRNAs are lncRNAs transcribed from the same strand of a coding gene, while antisense lncRNAs are lncRNAs transcribed from the opposite strand of a coding gene.
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Figure 1. Classification of lncRNAs based on genomic locations with: (A) intergenic lncRNA; (B) intronic lncRNA; (C) sense lncRNA; and (D) antisense lncRNA.
lncRNAs can also be divided into cis-acting or trans-acting lncRNAs based on their functional type [10][11]. lncRNAs acting as cis-regulators are mainly involved in the expression and function of their neighborhood coding genes, which are also likely to show expression correlation with coding genes. Examples for cis-acting lncRNAs include lncRNA VIM-AS1 and CARMEN [12][13]. On the other hand, trans-regulatory lncRNAs are involved in the regulation of distal genes from their transcription sites, where lncRNA FIRRE is an example [14]. However, with the progression in understanding lncRNA function, lncRNAs with both cis- and trans-regulatory functions have been identified, where the lncRNA lncKdm2b is an example [15][16].

2.2. Neighborhood Antisense lncRNAs to Sense Genes

An antisense transcript refers to a transcript generated from the opposite strand to a protein-coding or sense strand [17]. The existence of antisense transcription is very common across different transcriptomes and these antisense transcripts are usually co-transcribed with their sense transcripts [18]. It has been demonstrated that more than 60% of the sense transcripts have antisense partners [17][19][20]. Antisense transcripts have been reported to have multiple functions in the regulation of gene expression, which have further impacts on human health and diseases [21][22].
lncRNAs have been identified to be one common type of antisense transcripts of coding genes and are involved in the regulation of function and expression of their neighborhood coding genes [23][24]. These antisense lncRNAs also have several special characteristics, which are similar to mRNAs. There are several structural similarities between the lncRNAs and mRNAs, where both can be multi-exonic, 5′-capped, and 3′-polyadenylated [25]. The processing of lncRNAs is also similar to mRNAs, where the RNA polymerase II is responsible for the synthesis and both RNAs need to be spliced [21]. The transcriptional activity of lncRNAs can also be regulated by special DNA elements in promoters and enhancers, where promoters can have different locations [26]. In some special cases, both the sense and antisense genes can be controlled by a same bidirectional promoter, which causes the co-expression of the sense and antisense gene pair [27].
There are several locations near a coding gene where antisense lncRNAs are likely to exist (Figure 2). However, it is still not clear how different locations affect the function of lncRNAs. Recent studies have found that these neighborhood lncRNAs might affect their nearby coding genes in multiple ways, including direct regulation of the coding genes or indirect involvement in the functional regulation of the coding genes.
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Figure 2. Genomic locations of antisense neighborhood lncRNAs to a sense coding gene. Depending on the relative locations towards the coding gene, neighborhood lncRNAs are categorized into several types: nearby to head, the 5’ end of the lncRNA is close to the 5’ end of the coding gene; head to head, the 5’ end of both genes are aligned together; overlapping, the antisense lncRNA overlaps with the sense coding gene; tail to tail, the 3’ end of both genes are aligned together; and nearby to tail, the 3’ end of the lncRNA is close to the 3’ end of the coding gene.

2.3. Neighborhood Antisense lncRNAs to TFs

Along with the advancements in the discovery of lncRNAs, there is an increasing amount of studies trying to identify lncRNAs that have special relationships with coding genes. These relationships include but are not limited to correlations in expression, spatial localization, and function [28][29][30]. There is increasing evidence showing that lncRNAs, including TF neighborhood antisense lncRNAs, are involved in the expression or functions of TFs in gene regulation [31]. In this section, several TF-lncRNA pairs are summarized and discussed (Table 1).
Table 1. Summary of TF-neighborhood lncRNA pairs.
GATA3-AS1 is a divergent lncRNA gene sharing a promoter region with the TF gene GATA3, encoding a master regulator in T helper 2 cell functions. In one study performed by Gibbons et al., GATA3-AS1 was found to control the expression of GATA3 gene as well as two interleukin genes, IL5 and IL13. Specifically, depletion of GATA3-AS1 resulted in a reduction in GATA3, IL5, and IL13 mRNA and protein levels, along with decreased T helper 2 cell polarization. This regulatory function of GATA3-AS1 was accomplished through the interaction with histone-modifying enzymes and the alteration of histone codes to its own gene locus, which is the shared promoter region of GATA3 [32].
GA-binding protein subunit beta-1 (GABPB1) is a TF known to regulate the transcription of various genes related to antioxidation process, including Peroxiredoxin 5 (PRDX5) [33]. lncRNA GABPB1-AS1 gene is an antisense RNA gene of the GABPB1 gene. GABPB1 protein was previously reported to respond to chemical-induced cellular stress [34]. A recent study showed that GABPB1-AS1 was able to affect the functions of GABPB1 by modulating the translation process of GABPB1 in HepG2 cells, an in vitro model for hepatocellular carcinoma (HCC). The upregulation of GABPB1-AS1 inhibited the translation of GABPB1, which further reduced the expression of peroxidase genes, including PRDX5, and accumulation of reactive oxygen species and lipid peroxidation in the cells [35].
Yin Yang 1 (YY1) is an ubiquitously expressed TF involved in the regulation of cell proliferation and differentiation [36]. In muscle cells or myoblasts, YY1 regulates genes involved in cell proliferation and differentiation by interacting with histone methyltransferase complex and altering histone markers on target genes [37]. Linc-YY1 gene is a divergently transcribed lncRNA gene located upstream of the YY1 coding gene. The employment of linc-YY1 loss- and gain-of-function assays in a mouse myoblast cell line showed that linc-YY1 was important in the myogenic differentiation and muscle regeneration processes, and modulation of linc-YY1 also affected YY1 target genes. This function of linc-YY1 was accomplished through interacting with YY1 directly and eviction of YY1/Polycomb repressive complex, a complex mediating histone methylation from promoter regions of target genes [38].
All these studies supported the idea that lncRNAs, especially neighborhood lncRNAs of TFs, might be involved in the function of these TFs.

2.4. Genomic Locations and Structures of HNF1α-AS1 and HNF4α-AS1

HNF1α-AS1, a neighbor antisense lncRNA gene of the human HNF1α gene, is located at human Chromosome 12 with a length of 39.04 kb, containing two exons and one intron. The coding gene HNF1α and noncoding gene HNF1α-AS1 formed a typical TF-lncRNA pair (Figure 3A).
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Figure 3. Genomic locations of HNF1α, HNF1α-AS1, HNF4α, and HNF4α-AS1: (A) locations of HNF1α and HNF1α-AS1 on human chromosome 12; and (B) locations of HNF4α and HNF4α-AS1 on human chromosome 20.
HNF4α-AS1, a neighbor antisense lncRNA gene of the human HNF4α gene, is located at human Chromosome 20 with a length of 17.96 kb, containing four exons and three introns. The HNF4α and HNF4α-AS1 genes also form a typical pair of coding and neighborhood antisense noncoding genes (Figure 3B).
The coding potentials of HNF1α and HNF1α-AS1 as well as HNF4α and HNF4α-AS1 were analyzed by the Coding Potential Calculator (http://cpc2.cbi.pku.edu.cn) [39]. The analysis results (Table 2) indicate that both HNF1α-AS1 and HNF4α-AS1 have low coding probabilities in comparison to HNF1α and HNF4α, which confirmed the noncoding features of HNF1α-AS1 and HNF4α-AS1.
Table 2. The coding potentials of HNF1α-AS1 and HNF4α-AS1.
The RNA transcripts of both coding genes of HNF1α and HNF4α and noncoding genes of HNF1α-AS1 and HNF4α-AS1 show tissue-specific distributions in normal human tissues. To compare the expression patterns between the coding and noncoding genes, the top 10 tissues expressing HNF1α, HNF1α-AS1, HNF4α, and HNF4α-AS1 in human are summarized and compared. The tissue distribution pattern of HNF1α mRNA was retrieved from the RNA-Seq Expression Data GTEx in 53 tissues from 570 donors and shows relatively higher expression levels in the stomach, small intestine, colon, liver, pancreas, and kidney, the major organs in the gastrointestinal (GI) tract (Figure 4) [40]. A similar pattern in the GI tract organs is also found for HNF1α-AS1 (Figure 4A), indicating that HNF1α-AS1 is expressed in the organs where HNF1α is expressed. These results may suggest that HNF1α-AS1 is possibly involved in the regulatory function of HNF1α in the GI tract organs. Similar tissue distribution patterns are also found between HNF4α and HNF4α-AS1 (Figure 4B). These similarities in tissue distribution might suggest functional connections between HNF1α and HNF1α-AS1 as well as between HNF4α and HNF4α-AS1.
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Figure 4. Top 10 tissues expressing HNF1α, HNF1α-AS1, HNF4α, and HNF4α-AS1 in human: (A) tissue expression patterns of HNF1α and HNF1α-AS1; and (B) tissue expression patterns of HNF4α and HNF4α-AS1. Data are from GTEx database (https://www.gtexportal.org/home/). TPM: transcripts per million.
In addition to the chromatin locations and tissue distribution, the structures of lncRNAs are also important for their function and mechanism of action. RNA molecules have been shown to adopt higher-order tertiary interactions [41]. Even though the relationships between lncRNA structure and functions are still not fully understood yet, identification of structural domains, which mediate the interactions between lncRNAs and other molecules, is critical for the characterization of lncRNA functions. The secondary structures of HNF1α-AS1 is predicated using RNAfold program (http://rna.tbi.univie.ac.at//cgi-bin/RNAWebSuite/RNAfold.cgi). The secondary structure of HNF4α-AS1 is not predicated as the sequence length of HNF4α-AS1 exceeds the upper limit of lncRNA FASTA input for the program.
As shown in Figure 5, HNF1α-AS1 is able to form a stable secondary structure based on minimum free energy calculation. Several domains are also observed on the secondary structure of HNF1α-AS1. However, it is still not very clear what molecules interact with these domains and it is still largely unknown how they impact on the functions of HNF1α-AS1.
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Figure 5. Predication of secondary structure of HNF1α-AS1 by RNAfold. The structure of HNF1α-AS1 is generated based on minimum free energy method. The colors indicate base-pair probabilities from low to high.
HNF1α and HNF4α are well-studied TFs involved in organ maturation, cell differentiation, and disease development. Both HNF1α and HNF4α can be detected during different stages of embryonic development and they participate in the development of multiple organs, including liver, colon, and pancreas [42][43][44]. HNF1α and HNF4α are also regarded as master regulators of the metabolic functions in human. The target genes of HNF1α and HNF4α are involved in lipid metabolism, bile acid synthesis, lipoprotein metabolism, glucose metabolism, amino acid metabolism, and xenobiotic metabolism [45][46][47][48][49]. Taking xenobiotic metabolism as an example, knockdown of HNF1α or HNF4α in mice or human primary hepatocytes led to downregulation of the mRNA expression of several cytochrome P450s (P450s), which play critical roles in metabolizing drugs [49][50]. In addition to normal physiological activities, HNF1α and HNF4α are also highly involved in several diseases. Genetic mutations in HNF1α or HNF4α gene are some of the most common causes of maturity-onset diabetes of the young (MODY), which is characterized by a non-insulin dependent form of diabetes in young people below the age of 25 [51]. The dysfunction of pancreatic beta cells and impaired insulin secretion because of HNF1α or HNF4α mutations are believed to be the pathological mechanisms to this type of disease. In addition to MODY, HNF1α and HNF4α are involved in other type of diseases, including other metabolic diseases, inflammatory diseases, and cancer [52][53][54][55]. HNF1α and HNF4α are reported to play different roles based on cancer types. In HCC, the transduction of HNF1α and HNF4α was showed to suppress the growth of HepG2 and Huh7 cells in vitro and to reduce the tumorigenicity of these cells after transplantation into mice, indicating a role of tumor suppressing of these TFs [56]. However, in pancreatic cancer, the role of HNF1α is controversial based on the results from two reports. Luo and his colleagues reported that HNF1α was a possible tumor suppressing gene in pancreatic cancer [57]. The results of immunohistochemistry showed that the level of HNF1α was significantly lower in pancreatic cancer tissues than normal pancreatic tissues. Furthermore, knockdown of HNF1α also led to increase proliferation and to decrease apoptosis in pancreatic cancer cell lines, which supported the conclusion that HNF1α plays a role in tumor suppressing. This conclusion was challenged by another report by Abel et al., in which the authors showed that overexpression of HNF1α increased the formation of pancreatic cancer stem cells and tumorsphere [58]. In summary, HNF1α and HNF4α are two very important TFs in human physiologic functions and diseases.
Comparing to the well identified functions of HNF1α and HNF4α, the underlying molecular mechanisms of how HNF1α and HNF4α perform these functions is still not clearly understood yet. As TFs in nature, HNF1α and HNF4α can regulate their target genes through directly binding to their promoter regions. Other than direct binding, some other mechanisms of HNF1α and HNF4α in gene regulation are still elusive and need to be identified. lncRNAs are found to serve as cofactors of several important regulatory proteins and to be involved in their functions. However, whether lncRNAs are also involved in the function of HNF1α and HNF4α is still not fully understood.

3. Relations of the Regulation of Expression between HNF1α and HNF1α-AS1 and between HNF4α and HNF4α-AS1

The knowledge regarding how the expression of HNF1α-AS1 and HNF4α-AS1 is regulated in cells is still very limited. According to the literature, these lncRNAs are regulated by their neighborhood gene-coded proteins, which are HNF1α and HNF4α.
One study identified HNF1α-AS1 as an HNF1α-regulated lncRNA by comparing expression of HNF1α-AS1 in Huh7 cells with overexpression or knockdown of HNF1α. This result was also confirmed by the existence of HNF1α response element in the promoter region of HNF1α-AS1 and the positive expression correlation between HNF1α and HNF1α-AS1 in several HCC cell lines and human HCC samples [59]. In addition, knockdown of HNF1α led to the depletion of HNF1α-AS1 RNA levels in Huh7 or HepaRG cells, which further indicated this regulation relationship [60][61]. Other proteins were also reported to regulate the expression of HNF1α-AS1. Early growth response protein 1, a TF involved in cancer development, was also reported to regulate expression of HNF1α-AS1 by directly binding to the promoter region of HNF1α-AS1 and activating its transcription [62].
Guo and Lu reported that the expression of HNF4α-AS1 was strongly activated by P1-HNF4α, which is predominantly produced in adult liver, but not P2-HNF4α, which is prevalent in fetal liver, pancreas, and liver/colon cancer. Therefore, HNF4α-AS1 might be a biomarker for P1-HNF4α expression and might be involved in the functional regulation of the liver-specific P1-HNF4α [63]. The knockdown of HNF4α also showed to repress the expression of HNF4α-AS1 in HepaRG cells, which further validated the idea the HNF4α-AS1 was regulated by HNF4α [60].
These studies suggested the expression regulatory hierarchy between these two TF-lncRNA pairs, where the expression of lncRNAs, HNF1α-AS1 and HNF4α-AS1, are regulated by their neighborhood TFs, HNF1α and HNF4α. However, there is still no clear evidence showing the direct binding of HNF1α to the HNF1α-AS1 promoter or HNF4α to the HNF4α-AS1 promoter. Whether HNF1α and HNF4α regulate HNF1α-AS1 and HNF4α-AS1 through direct binding or there are still other regulatory mechanisms between the TFs and lncRNAs are still not understood. Future studies would be needed to address these questions.

4. Functions of HNF1α-AS1 and HNF4α-AS1 in Human Physiology and Diseases

4.1. lncRNAs in Human Physiology and Diseases

lncRNAs have been found to highly involved in both normal physiological activities and diseases in human health [64][65].
Numerous lncRNAs have been found to play critical roles in the processes of development, including organ development and embryogenesis. LncRNA FENDRR, a divergent lncRNA of TF FOXF1, was one of the examples reported to be involved in organ development. Knockdown of FENDRR in mice led to defects in multiple organs, including the heart, lung, and gastrointestinal tract [66]. Another example lncRNA, NEAT1, was reported to be involved in the development of mammary glands and pregnancy in mice [67]. Other than development, lncRNAs have been found in other physiological processes, such as energy metabolism, circadian rhythm, and spermatogenesis [68][69][70].
Diseases related lncRNAs are extensively studied recently. Utilizing the sequencing techniques, thousands of differentially expressed lncRNAs with potential implications in the initiation, progression, and treatment of all kinds of diseases have been identified and studied. In a comprehensive study comparing the transcriptome among more than 7000 samples, including tumor tissues, normal tissues, and tumor cell lines, thousands of cancer-related lncRNAs have been identified [71]. This study opened up the research of using lncRNAs as biomarkers for cancer types, progression, or treatment strategies. In recent years, more and more cancer-related lncRNAs have been identified and functionally characterized [72]. Aside from cancer, lncRNAs are also important for other diseases. For example, lncRNA BACE1-AS is reported to have a strong correlation with Alzheimer’s disease and lncRNA MHRT is involved in cardiovascular diseases [73][74].

4.2. Roles of HNF1α-AS1 and HNF4α-AS1 in Physiologic Functions, including Drug Metabolism

HNF1α-AS1 and HNF4α-AS1 were recently reported to be involved in the hepatic metabolic function and drug metabolism through affecting P450 genes and related TFs [60][61][75].
Using a lncRNA specific microarray assay, the differences of lncRNA expression were compared between human liver samples with high and low CYP3A4 expression. HNF1α-AS1 was identified as one of the differentially expressed lncRNAs [61]. In addition, positive correlations were identified in human liver samples between the expression of HNF1α-AS1 and CYP2C8, 2C9, 2C19, 2D6, 2E1, 3A4, pregnane X receptor (PXR), constitutive androstane receptor (CAR), and HNF1α, which implicated the involvement of HNF1α-AS1 in regulating drug metabolizing enzymes (DMEs) and related TFs in the liver. The functions of HNF1α-AS1 was further studied by generating loss-of-function models in HepaRG and Huh7cell lines. In both cell lines, knockdown of HNF1α-AS1 led to decreases in mRNA expression of several major P450s involved in drug metabolism, as well as P450 related TFs [60][61]. Interestingly, HNF4α-AS1 was reported to have opposite regulatory effects comparing to HNF1α-AS1. Specifically, knockdown of HNF4α-AS1 in HepaRG cells resulted in induction of several P450s, including CYP1A2, 2B6, 2C8, 2C9, 2C19, 2E1, and 3A4, as well as P450 related TFs PXR and CAR [60].
In a follow-up study performed by Chen and his colleagues, knockdown of HNF1α-AS1 or HNF4α-AS1 also caused alterations in the susceptibility of acetaminophen (APAP)-induced cytotoxicity in HepaRG cells [75]. The metabolic pathway analysis showed that the alterations of toxicity were primarily caused by the changes in APAP-metabolizing P450s in both mRNA and protein levels. These reported physiological roles of HNF1α-AS1 and HNF4α-AS1 are summarized and displayed in Figure 6.
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Figure 6. HNF1α-AS1 and HNF4α-AS1 in hepatic metabolism. HNF1α-AS1 is able to positively regulate the expression of PXR, CAR, and several P450s. HNF1α-AS1 also affected APAP-induced toxicity by regulating the expression and function of APAP-metabolizing P450s. Meanwhile, HNF4α-AS1 is able to negatively regulate the expression of PXR, CAR, P450s, and APAP-induced toxicity.
These results indicate that the lncRNAs HNF1α-AS1 and HNF4α-AS1 are involved in the normal physiological functions of the liver by regulating the metabolic functions. Recent studies have suggested that lncRNAs are highly relevant to drug metabolism through the regulation of drug metabolizing enzyme genes [76][77][78]. In addition to HNF1α-AS1 and HNF4α-AS1, several other lncRNAs have also been identified in the regulation of expression of drug metabolizing enzyme genes, such as LINC00574 in the regulation of UGT2B15 expression, and contribution to susceptibility of drug-induced liver injury (DILI), for example LINC00844 [79][80]. These works have opened a novel area in the field of drug metabolism and DILI, which requires further studies to provide answers for some fundamental questions.

4.3. Role of HNF1α-AS1 and HNF4α-AS1 in the Progress of Human Diseases, including Cancers

Several functions of HNF1α-AS1 and HNF4α-AS1 in human diseases have been reported in publications. In this section, the identified functions of HNF1α-AS1 and HNF4α-AS1 in human diseases are summarized and discussed.
Currently, numerous studies have shown that HNF1α-AS1 is actively involved in different stages of cancer, including tumorigenesis, progression, and treatment. Significantly differentially expressed HNF1α-AS1 has been found in several types of cancer tissues comparing to normal tissues, including the liver, colon, lung, cervical, stomach, and bladder. However, the regulation patterns are different. Specifically, HNF1α-AS1 is upregulated in esophageal, lung, bladder, and colon cancers and downregulated in gastric and pancreatic cancers [81][82][83][84][85][86]. These results indicate that HNF1α-AS1 might have tissue-specific functions. Most studies showed that the high expression levels of HNF1α-AS1 were associated with a poor prognosis, a higher risk of metastasis, and a lower overall survival rate in cancers [82][85][87][88][89].
HNF1α-AS1 plays a contradictory role in the development of cancer. According to current studies, HNF1α-AS1 was reported to function as both oncogene and tumor-suppressing gene in different cancers. Zhang et al. reported that HNF1α-AS1 promoted carcinogenesis in colorectal cancer by activating the Wnt/β-catenin signaling pathway, indicating that HNF1α-AS1 might be used as a prognostic biomarker in colorectal cancer [90]. In HCC, HNF1α-AS1 was reported to work as a tumor repressor by decreasing tumor growth and metastasis [59]. However, two other studies focusing on the roles of HNF1α-AS1 in HCC defined HNF1α-AS1 as an oncogene based on its function to promote cell proliferation and hepatocarcinogenesis [89][91].
For the progression of cancer, HNF1α-AS1 mainly regulates tumor growth and metastasis. Knockdown of HNF1α-AS1 was reported to reduce cell proliferation rates in several in vitro cancer cell lines, which might further affect tumor growth [88][92][93]. Metastasis is another major activity during cancer progression. HNF1α-AS1 was also reported to be involved in cancer metastasis by regulating cell migration, invasion, colony formation, and epithelial–mesenchymal transition (EMT), and knockdown of HNF1α-AS1 resulted in decreased cell movement or invasion, which might further impact the metastasis of tumor [85][88][92][93][94][95]. In this part of function, HNF1α-AS1 was involved in the several signaling pathways to promote cell survival and movement, including the CDK signaling pathway, p53 pathway, and the Akt-mTOR/GSK3β signaling pathway.
Drug resistance is the major cause of treatment failure in cancer treatment. Several mechanisms have been identified to contribute to the development of drug resistance in cancer cells, including promoted cell survival and altered drug metabolism [96]. The expression of HNF1α-AS1 was reported to affect the sensitivity of cancer cells to anti-cancer drugs. Cisplatin is a widely used chemotherapeutic drug for the treatment of cervical cancer. In one study performed by Luo et al., knockdown of HNF1α-AS1 in cisplatin-resistant HeLa re-sensitized the cells to cisplatin treatment, indicating that HNF1α-AS1 was involved in the regulation of drug resistance in cancer cells [97].
In summary, based on the findings in the current published articles, HNF1α-AS1 is an important regulatory molecule in cancer biology. However, controversy still exists in the roles of HNF1α-AS1 in cancers and future studies are needed to clarify the functions of HNF1α-AS1.
In terms of HNF4α-AS1, the functional study is still very limited. HNF4α-AS1 was found to be differentially expressed in HCC compared with adjacent cirrhotic tissues using RNA sequencing techniques, indicating that HNF4α-AS1 may function as a biomarker for the development of HCC in patients with cirrhosis [98]. Using co-expression and functional annotation enrichment analyses across several tissues and cell types, Haberman and his colleagues reported that HNF4α-AS1 was significantly downregulated in patients with Crohn’s disease, where the expression of HNF4α-AS1 also showed association with an epithelial metabolic signature, indicating that HNF4α-AS1 might be a novel inflammatory signal or therapeutic target for Crohn’s disease [99].

This entry is adapted from the peer-reviewed paper 10.3390/ncrna6020024

References

  1. Szymanski, M.; Barciszewski, J. Beyond the proteome: Non-coding regulatory RNAs. Genome Biol. 2002, 3, 1–8.
  2. Choi, S.W.; Kim, H.W.; Nam, J.W. The small peptide world in long noncoding RNAs. Brief. Bioinform. 2019, 20, 1853–1864.
  3. Chen, J.; Brunner, A.D.; Cogan, J.Z.; Nunez, J.K.; Fields, A.P.; Adamson, B.; Itzhak, D.N.; Li, J.Y.; Mann, M.; Leonetti, M.D.; et al. Pervasive functional translation of noncanonical human open reading frames. Science 2020, 367, 1140–1146.
  4. Eddy, S.R. Non-coding RNA genes and the modern RNA world. Nat. Rev. Genet. 2001, 2, 919–929.
  5. Frankish, A.; Diekhans, M.; Ferreira, A.M.; Johnson, R.; Jungreis, I.; Loveland, J.; Mudge, J.M.; Sisu, C.; Wright, J.; Armstrong, J.; et al. GENCODE reference annotation for the human and mouse genomes. Nucleic Acids Res. 2019, 47, D766–D773.
  6. Volders, P.J.; Anckaert, J.; Verheggen, K.; Nuytens, J.; Martens, L.; Mestdagh, P.; Vandesompele, J. LNCipedia 5: Towards a reference set of human long non-coding RNAs. Nucleic Acids Res. 2019, 47, D135–D139.
  7. Fang, S.; Zhang, L.; Guo, J.; Niu, Y.; Wu, Y.; Li, H.; Zhao, L.; Li, X.; Teng, X.; Sun, X.; et al. NONCODEV5: A comprehensive annotation database for long non-coding RNAs. Nucleic Acids Res. 2018, 46, D308–D314.
  8. Consortium, E.P. An integrated encyclopedia of DNA elements in the human genome. Nature 2012, 489, 57–74.
  9. Rinn, J.L.; Chang, H.Y. Genome regulation by long noncoding RNAs. Annu. Rev. Biochem. 2012, 81, 145–166.
  10. Mercer, T.R.; Mattick, J.S. Structure and function of long noncoding RNAs in epigenetic regulation. Nat. Struct. Mol. Biol. 2013, 20, 300–307.
  11. Guil, S.; Esteller, M. Cis-acting noncoding RNAs: Friends and foes. Nat. Struct. Mol. Biol. 2012, 19, 1068–1075.
  12. Boque-Sastre, R.; Soler, M.; Oliveira-Mateos, C.; Portela, A.; Moutinho, C.; Sayols, S.; Villanueva, A.; Esteller, M.; Guil, S. Head-to-head antisense transcription and R-loop formation promotes transcriptional activation. Proc. Natl. Acad. Sci. USA 2015, 112, 5785–5790.
  13. Ounzain, S.; Micheletti, R.; Arnan, C.; Plaisance, I.; Cecchi, D.; Schroen, B.; Reverter, F.; Alexanian, M.; Gonzales, C.; Ng, S.Y.; et al. CARMEN, a human super enhancer-associated long noncoding RNA controlling cardiac specification, differentiation and homeostasis. J. Mol. Cell. Cardiol 2015, 89, 98–112.
  14. Lewandowski, J.P.; Lee, J.C.; Hwang, T.; Sunwoo, H.; Goldstein, J.M.; Groff, A.F.; Chang, N.P.; Mallard, W.; Williams, A.; Henao-Meija, J.; et al. The Firre locus produces a trans-acting RNA molecule that functions in hematopoiesis. Nat. Commun. 2019, 10, 5137.
  15. Li, W.; Shen, W.; Zhang, B.; Tian, K.; Li, Y.; Mu, L.; Luo, Z.; Zhong, X.; Wu, X.; Liu, Y.; et al. Long non-coding RNA LncKdm2b regulates cortical neuronal differentiation by cis-activating Kdm2b. Protein Cell 2020, 11, 161–186.
  16. Liu, B.; Ye, B.; Yang, L.; Zhu, X.; Huang, G.; Zhu, P.; Du, Y.; Wu, J.; Qin, X.; Chen, R. Long noncoding RNA lncKdm2b is required for ILC3 maintenance by initiation of Zfp292 expression. Nat. Immunol. 2017, 18, 499.
  17. Katayama, S.; Tomaru, Y.; Kasukawa, T.; Waki, K.; Nakanishi, M.; Nakamura, M.; Nishida, H.; Yap, C.C.; Suzuki, M.; Kawai, J.; et al. Antisense transcription in the mammalian transcriptome. Science 2005, 309, 1564–1566.
  18. Numata, K.; Kiyosawa, H. Genome-wide impact of endogenous antisense transcripts in eukaryotes. Front. Biosci. 2012, 17, 300–315.
  19. Nishizawa, M.; Okumura, T.; Ikeya, Y.; Kimura, T. Regulation of inducible gene expression by natural antisense transcripts. Front. Biosci. 2012, 17, 938–958.
  20. Rosikiewicz, W.; Makalowska, I. Biological functions of natural antisense transcripts. Acta Biochim. Pol. 2016, 63, 665–673.
  21. Latgé, G.; Poulet, C.; Bours, V.; Josse, C.; Jerusalem, G. Natural antisense transcripts: Molecular mechanisms and implications in breast cancers. Int. J. Mol. Sci. 2018, 19, 123.
  22. Wanowska, E.; Kubiak, M.R.; Rosikiewicz, W.; Makalowska, I.; Szczesniak, M.W. Natural antisense transcripts in diseases: From modes of action to targeted therapies. Wiley Interdiscip. Rev. RNA 2018, 9.
  23. Joung, J.; Engreitz, J.M.; Konermann, S.; Abudayyeh, O.O.; Verdine, V.K.; Aguet, F.; Gootenberg, J.S.; Sanjana, N.E.; Wright, J.B.; Fulco, C.P.; et al. Genome-scale activation screen identifies a lncRNA locus regulating a gene neighbourhood. Nature 2017, 548, 343–346.
  24. Dempsey, J.; Zhang, A.; Cui, J.Y. Coordinate regulation of long non-coding RNAs and protein-coding genes in germ-free mice. BMC Genom. 2018, 19, 834.
  25. Guttman, M.; Amit, I.; Garber, M.; French, C.; Lin, M.F.; Feldser, D.; Huarte, M.; Zuk, O.; Carey, B.W.; Cassady, J.P.; et al. Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals. Nature 2009, 458, 223–227.
  26. Lin, S.; Zhang, L.; Luo, W.; Zhang, X. Characteristics of antisense transcript promoters and the regulation of their activity. Int. J. Mol. Sci. 2016, 17, 9.
  27. Uesaka, M.; Nishimura, O.; Go, Y.; Nakashima, K.; Agata, K.; Imamura, T. Bidirectional promoters are the major source of gene activation-associated non-coding RNAs in mammals. BMC Genom. 2014, 15, 35.
  28. Herriges, M.J.; Swarr, D.T.; Morley, M.P.; Rathi, K.S.; Peng, T.; Stewart, K.M.; Morrisey, E.E. Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development. Genes Dev. 2014, 28, 1363–1379.
  29. Cao, Y.; Wang, J.; Lu, X.; Kong, X.; Bo, C.; Li, S.; Li, J.; Sun, X.; Wang, N.; Tian, K.; et al. Construction of a long noncoding RNAmediated transcription factor and gene regulatory triplet network reveals global patterns and biomarkers for ischemic stroke. Int. J. Mol. Med. 2020, 45, 333–342.
  30. Gil, N.; Ulitsky, I. Regulation of gene expression by cis-acting long non-coding RNAs. Nat. Rev. Genet. 2020, 21, 102–117.
  31. Villegas, V.E.; Zaphiropoulos, P.G. Neighboring gene regulation by antisense long non-coding RNAs. Int. J. Mol. Sci. 2015, 16, 3251–3266.
  32. Gibbons, H.R.; Shaginurova, G.; Kim, L.C.; Chapman, N.; Spurlock, C.F., 3rd; Aune, T.M. Divergent lncRNA GATA3-AS1 Regulates GATA3 Transcription in T-Helper 2 Cells. Front. Immunol. 2018, 9, 2512.
  33. Usmanova, N.; Tomilin, N.; Zhivotovsky, B.; Kropotov, A. Transcription factor GABP/NRF-2 controlling biogenesis of mitochondria regulates basal expression of peroxiredoxin V but the mitochondrial function of peroxiredoxin V is dispensable in the dog. Biochimie 2011, 93, 306–313.
  34. Tani, H.; Torimura, M. Identification of short-lived long non-coding RNAs as surrogate indicators for chemical stress response. Biochem. Biophys. Res. Commun. 2013, 439, 547–551.
  35. Qi, W.; Li, Z.; Xia, L.; Dai, J.; Zhang, Q.; Wu, C.; Xu, S. LncRNA GABPB1-AS1 and GABPB1 regulate oxidative stress during erastin-induced ferroptosis in HepG2 hepatocellular carcinoma cells. Sci. Rep. 2019, 9, 16185.
  36. Deng, Z.; Cao, P.; Wan, M.M.; Sui, G. Yin Yang 1: A multifaceted protein beyond a transcription factor. Transcription 2010, 1, 81–84.
  37. Wang, H.; Hertlein, E.; Bakkar, N.; Sun, H.; Acharyya, S.; Wang, J.; Carathers, M.; Davuluri, R.; Guttridge, D.C. NF-κB regulation of YY1 inhibits skeletal myogenesis through transcriptional silencing of myofibrillar genes. Mol. Cell. Biol. 2007, 27, 4374–4387.
  38. Zhou, L.; Sun, K.; Zhao, Y.; Zhang, S.; Wang, X.; Li, Y.; Lu, L.; Chen, X.; Chen, F.; Bao, X.; et al. Linc-YY1 promotes myogenic differentiation and muscle regeneration through an interaction with the transcription factor YY1. Nat. Commun. 2015, 6, 10026.
  39. Kang, Y.J.; Yang, D.C.; Kong, L.; Hou, M.; Meng, Y.Q.; Wei, L.; Gao, G. CPC2: A fast and accurate coding potential calculator based on sequence intrinsic features. Nucleic Acids Res. 2017, 45, W12–W16.
  40. Consortium, G.T. The Genotype-Tissue Expression (GTEx) project. Nat. Genet. 2013, 45, 580–585.
  41. Wan, Y.; Kertesz, M.; Spitale, R.C.; Segal, E.; Chang, H.Y. Understanding the transcriptome through RNA structure. Nat. Rev. Genet. 2011, 12, 641–655.
  42. Ott, M.-O.; Rey-Campos, J.; Cereghini, S.; Yaniv, M. vHNF1 is expressed in epithelial cells of distinct embryonic origin during development and precedes HNF1 expression. Mech. Dev. 1991, 36, 47–58.
  43. Shih, D.Q.; Stoffel, M. Dissecting the transcriptional network of pancreatic islets during development and differentiation. Proc. Natl. Acad. Sci. USA 2001, 98, 14189–14191.
  44. Garrison, W.D.; Battle, M.A.; Yang, C.; Kaestner, K.H.; Sladek, F.M.; Duncan, S.A. Hepatocyte nuclear factor 4α is essential for embryonic development of the mouse colon. Gastroenterology 2006, 130, 19-e1.
  45. Chiang, J.Y. Hepatocyte nuclear factor 4α regulation of bile acid and drug metabolism. Expert Opin. Drug Metab. Toxicol. 2009, 5, 137–147.
  46. Shih, D.Q.; Bussen, M.; Sehayek, E.; Ananthanarayanan, M.; Shneider, B.L.; Suchy, F.J.; Shefer, S.; Bollileni, J.S.; Gonzalez, F.J.; Breslow, J.L. Hepatocyte nuclear factor-1α is an essential regulator of bile acid and plasma cholesterol metabolism. Nat. Genet. 2001, 27, 375–382.
  47. Pontoglio, M. Hepatocyte nuclear factor 1, a transcription factor at the crossroads of glucose homeostasis. J. Am. Soc. Nephrol. 2000, 11, S140–S143.
  48. Pontoglio, M.; Sreenan, S.; Roe, M.; Pugh, W.; Ostrega, D.; Doyen, A.; Pick, A.J.; Baldwin, A.; Velho, G.; Froguel, P.; et al. Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice. J. Clin. Investig. 1998, 101, 2215–2222.
  49. Cheung, C.; Akiyama, T.E.; Kudo, G.; Gonzalez, F.J. Hepatic expression of cytochrome P450s in hepatocyte nuclear factor 1-alpha (HNF1alpha)-deficient mice. Biochem. Pharmacol. 2003, 66, 2011–2020.
  50. Kamiyama, Y.; Matsubara, T.; Yoshinari, K.; Nagata, K.; Kamimura, H.; Yamazoe, Y. Role of human hepatocyte nuclear factor 4α in the expression of drug-metabolizing enzymes and transporters in human hepatocytes assessed by use of small interfering RNA. Drug Metab. Pharm. 2007, 22, 287–298.
  51. Anik, A.; Catli, G.; Abaci, A.; Bober, E. Maturity-onset diabetes of the young (MODY): An update. J. Pediatric Endocrinol. Metab. 2015, 28, 251–263.
  52. Babeu, J.P.; Boudreau, F. Hepatocyte nuclear factor 4-alpha involvement in liver and intestinal inflammatory networks. World J. Gastroenterol. 2014, 20, 22–30.
  53. Patitucci, C.; Couchy, G.; Bagattin, A.; Caneque, T.; de Reynies, A.; Scoazec, J.Y.; Rodriguez, R.; Pontoglio, M.; Zucman-Rossi, J.; Pende, M.; et al. Hepatocyte nuclear factor 1alpha suppresses steatosis-associated liver cancer by inhibiting PPARgamma transcription. J. Clin. Investig. 2017, 127, 1873–1888.
  54. Lu, Y.; Xu, D.; Peng, J.; Luo, Z.; Chen, C.; Chen, Y.; Chen, H.; Zheng, M.; Yin, P.; Wang, Z. HNF1A inhibition induces the resistance of pancreatic cancer cells to gemcitabine by targeting ABCB1. EBioMedicine 2019, 44, 403–418.
  55. Bonzo, J.A.; Patterson, A.D.; Krausz, K.W.; Gonzalez, F.J. Metabolomics identifies novel Hnf1α-dependent physiological pathways in vivo. Mol. Endocrinol. 2010, 24, 2343–2355.
  56. Takashima, Y.; Horisawa, K.; Udono, M.; Ohkawa, Y.; Suzuki, A. Prolonged inhibition of hepatocellular carcinoma cell proliferation by combinatorial expression of defined transcription factors. Cancer Sci. 2018, 109, 3543–3553.
  57. Luo, Z.; Li, Y.; Wang, H.; Fleming, J.; Li, M.; Kang, Y.; Zhang, R.; Li, D. Hepatocyte nuclear factor 1A (HNF1A) as a possible tumor suppressor in pancreatic cancer. PLoS ONE 2015, 10, e0121082.
  58. Abel, E.V.; Goto, M.; Magnuson, B.; Abraham, S.; Ramanathan, N.; Hotaling, E.; Alaniz, A.A.; Kumar-Sinha, C.; Dziubinski, M.L.; Urs, S. HNF1A is a novel oncogene that regulates human pancreatic cancer stem cell properties. Elife 2018, 7, e33947.
  59. Ding, C.H.; Yin, C.; Chen, S.J.; Wen, L.Z.; Ding, K.; Lei, S.J.; Liu, J.P.; Wang, J.; Chen, K.X.; Jiang, H.L.; et al. The HNF1alpha-regulated lncRNA HNF1A-AS1 reverses the malignancy of hepatocellular carcinoma by enhancing the phosphatase activity of SHP-1. Mol. Cancer 2018, 17, 63.
  60. Chen, L.; Bao, Y.; Piekos, S.C.; Zhu, K.; Zhang, L.; Zhong, X.B. A Transcriptional Regulatory Network Containing Nuclear Receptors and Long Noncoding RNAs Controls Basal and Drug-Induced Expression of Cytochrome P450s in HepaRG Cells. Mol. Pharmacol. 2018, 94, 749–759.
  61. Wang, Y.; Yan, L.; Liu, J.; Chen, S.; Liu, G.; Nie, Y.; Wang, P.; Yang, W.; Chen, L.; Zhong, X. The HNF1α-regulated lncRNA HNF1α-AS1 is Involved in the Regulation of Cytochrome P450 Expression in Human Liver Tissues and Huh7 Cells. J. Pharmacol. Exp. Ther. 2019, 368, 353–362.
  62. Liu, H.T.; Liu, S.; Liu, L.; Ma, R.R.; Gao, P. EGR1-Mediated Transcription of lncRNA-HNF1A-AS1 Promotes Cell-Cycle Progression in Gastric Cancer. Cancer Res. 2018, 78, 5877–5890.
  63. Guo, S.; Lu, H. Novel mechanisms of regulation of the expression and transcriptional activity of hepatocyte nuclear factor 4α. J. Cell. Biochem. 2019, 120, 519–532.
  64. Melissari, M.T.; Grote, P. Roles for long non-coding RNAs in physiology and disease. Pflug. Arch. Eur. J. Physiol. 2016, 468, 945–958.
  65. Kopp, F. Molecular functions and biological roles of long non-coding RNAs in human physiology and disease. J. Gene Med. 2019, 21, e3104.
  66. Sauvageau, M.; Goff, L.A.; Lodato, S.; Bonev, B.; Groff, A.F.; Gerhardinger, C.; Sanchez-Gomez, D.B.; Hacisuleyman, E.; Li, E.; Spence, M.; et al. Multiple knockout mouse models reveal lincRNAs are required for life and brain development. Elife 2013, 2, e01749.
  67. Clemson, C.M.; Hutchinson, J.N.; Sara, S.A.; Ensminger, A.W.; Fox, A.H.; Chess, A.; Lawrence, J.B. An architectural role for a nuclear noncoding RNA: NEAT1 RNA is essential for the structure of paraspeckles. Mol. Cell 2009, 33, 717–726.
  68. Giroud, M.; Scheideler, M. Long Non-Coding RNAs in Metabolic Organs and Energy Homeostasis. Int. J. Mol. Sci. 2017, 18.
  69. Fan, Z.; Zhao, M.; Joshi, P.D.; Li, P.; Zhang, Y.; Guo, W.; Xu, Y.; Wang, H.; Zhao, Z.; Yan, J. A class of circadian long non-coding RNAs mark enhancers modulating long-range circadian gene regulation. Nucleic Acids Res. 2017, 45, 5720–5738.
  70. Sahlu, B.W.; Zhao, S.; Wang, X.; Umer, S.; Zou, H.; Huang, J.; Zhu, H. Long noncoding RNAs: New insights in modulating mammalian spermatogenesis. J. Anim. Sci. Biotechnol. 2020, 11, 16.
  71. Iyer, M.K.; Niknafs, Y.S.; Malik, R.; Singhal, U.; Sahu, A.; Hosono, Y.; Barrette, T.R.; Prensner, J.R.; Evans, J.R.; Zhao, S.; et al. The landscape of long noncoding RNAs in the human transcriptome. Nat. Genet. 2015, 47, 199–208.
  72. Huarte, M. The emerging role of lncRNAs in cancer. Nat. Med. 2015, 21, 1253–1261.
  73. Faghihi, M.A.; Modarresi, F.; Khalil, A.M.; Wood, D.E.; Sahagan, B.G.; Morgan, T.E.; Finch, C.E.; Laurent, G.S., III; Kenny, P.J.; Wahlestedt, C. Expression of a noncoding RNA is elevated in Alzheimer’s disease and drives rapid feed-forward regulation of β-secretase. Nat. Med. 2008, 14, 723–730.
  74. Han, P.; Li, W.; Lin, C.H.; Yang, J.; Shang, C.; Nuernberg, S.T.; Jin, K.K.; Xu, W.; Lin, C.Y.; Lin, C.J.; et al. A long noncoding RNA protects the heart from pathological hypertrophy. Nature 2014, 514, 102–106.
  75. Chen, L.; Wang, P.; Manautou, J.E.; Zhong, X.B. Knockdown of Long Noncoding RNAs Hepatocyte Nuclear Factor 1alpha Antisense RNA 1 and Hepatocyte Nuclear Factor 4alpha Antisense RNA 1 Alters Susceptibility of Acetaminophen-Induced Cytotoxicity in HepaRG Cells. Mol. Pharmacol. 2020, 97, 278–286.
  76. Wang, Y.; Fang, Z.; Hong, M.; Yang, D.; Xie, W. Long-noncoding RNAs (lncRNAs) in drug metabolism and disposition, implications in cancer chemo-resistance. Acta Pharm. Sin. B 2020, 10, 105–112.
  77. Pan, J.J.; Xie, X.J.; Li, X.; Chen, W. Long Non-coding RNAs and Drug Resistance. Asian Pac. J. Cancer Prev. 2015, 16, 8067–8073.
  78. Ning, B.; Yu, D.; Yu, A.M. Advances and challenges in studying noncoding RNA regulation of drug metabolism and development of RNA therapeutics. Biochem. Pharm. 2019, 169, 113638.
  79. Yu, D.; Chen, J.; Chen, S.; Xu, L.; Wu, L.; Li, D.; Luo, J.; Jin, Y.; Zhao, Y.; Knox, B.; et al. Coordinated Regulation of UGT2B15 Expression by Long Noncoding RNA LINC00574 and hsa-miR-129-5p in HepaRG Cells. Drug Metab. Dispos. 2020, 48, 297–306.
  80. Li, D.; Wu, L.; Knox, B.; Chen, S.; Tolleson, W.H.; Liu, F.; Yu, D.; Guo, L.; Tong, W.; Ning, B. Long noncoding RNA LINC00844-mediated molecular network regulates expression of drug metabolizing enzymes and nuclear receptors in human liver cells. Arch. Toxicol. 2020.
  81. Yang, X.; Song, J.H.; Cheng, Y.; Wu, W.; Bhagat, T.; Yu, Y.; Abraham, J.M.; Ibrahim, S.; Ravich, W.; Roland, B.C.; et al. Long non-coding RNA HNF1A-AS1 regulates proliferation and migration in oesophageal adenocarcinoma cells. Gut 2014, 63, 881–890.
  82. Cai, L.; Lv, J.; Zhang, Y.; Li, J.; Wang, Y.; Yang, H. The lnc RNA HNF 1A-AS 1 is a negative prognostic factor and promotes tumorigenesis in osteosarcoma. J. Cell. Mol. Med. 2017, 21, 2654–2662.
  83. Dang, Y.; Lan, F.; Ouyang, X.; Wang, K.; Lin, Y.; Yu, Y.; Wang, L.; Wang, Y.; Huang, Q. Expression and clinical significance of long non-coding RNA HNF1A-AS1 in human gastric cancer. World J. Surg. Oncol. 2015, 13, 302.
  84. Zhan, Y.; Li, Y.; Guan, B.; Wang, Z.; Peng, D.; Chen, Z.; He, A.; He, S.; Gong, Y.; Li, X. Long non-coding RNA HNF1A-AS1 promotes proliferation and suppresses apoptosis of bladder cancer cells through upregulating Bcl-2. Oncotarget 2017, 8, 76656.
  85. Fang, C.; Qiu, S.; Sun, F.; Li, W.; Wang, Z.; Yue, B.; Wu, X.; Yan, D. Long non-coding RNA HNF1A-AS1 mediated repression of miR-34a/SIRT1/p53 feedback loop promotes the metastatic progression of colon cancer by functioning as a competing endogenous RNA. Cancer Lett. 2017, 410, 50–62.
  86. Muller, S.; Raulefs, S.; Bruns, P.; Afonso-Grunz, F.; Plotner, A.; Thermann, R.; Jager, C.; Schlitter, A.M.; Kong, B.; Regel, I.; et al. Next-generation sequencing reveals novel differentially regulated mRNAs, lncRNAs, miRNAs, sdRNAs and a piRNA in pancreatic cancer. Mol. Cancer 2015, 14, 94.
  87. Ma, Y.F.; Liang, T.; Li, C.R.; Li, Y.J.; Jin, S.; Liu, Y. Long non-coding RNA HNF1A-AS1 up-regulation in non-small cell lung cancer correlates to poor survival. Eur. Rev. Med. Pharm. Sci. 2016, 20, 4858–4863.
  88. Zhao, H.; Hou, W.; Tao, J.; Zhao, Y.; Wan, G.; Ma, C.; Xu, H. Upregulation of lncRNA HNF1A-AS1 promotes cell proliferation and metastasis in osteosarcoma through activation of the Wnt/beta-catenin signaling pathway. Am. J. Transl. Res. 2016, 8, 3503–3512.
  89. Liu, Z.; Wei, X.; Zhang, A.; Li, C.; Bai, J.; Dong, J. Long non-coding RNA HNF1A-AS1 functioned as an oncogene and autophagy promoter in hepatocellular carcinoma through sponging hsa-miR-30b-5p. Biochem. Biophys. Res. Commun. 2016, 473, 1268–1275.
  90. Zhang, X.; Xiong, Y.; Tang, F.; Bian, Y.; Chen, Y.; Zhang, F. Long noncoding RNA HNF1A-AS1 indicates a poor prognosis of colorectal cancer and promotes carcinogenesis via activation of the Wnt/beta-catenin signaling pathway. Biomed. Pharmacother. Biomed. Pharmacother. 2017, 96, 877–883.
  91. Wang, C.; Mou, L.; Chai, H.X.; Wang, F.; Yin, Y.Z.; Zhang, X.Y. Long non-coding RNA HNF1A-AS1 promotes hepatocellular carcinoma cell proliferation by repressing NKD1 and P21 expression. Biomed. Pharmacother. Biomed. Pharmacother. 2017, 89, 926–932.
  92. Wu, Y.; Liu, H.; Shi, X.; Yao, Y.; Yang, W.; Song, Y. The long non-coding RNA HNF1A-AS1 regulates proliferation and metastasis in lung adenocarcinoma. Oncotarget 2015, 6, 9160–9172.
  93. Zhang, G.; An, X.; Zhao, H.; Zhang, Q.; Zhao, H. Long non-coding RNA HNF1A-AS1 promotes cell proliferation and invasion via regulating miR-17-5p in non-small cell lung cancer. Biomed. Pharm. 2018, 98, 594–599.
  94. Guo, X.; Zhang, Y.; Liu, L.; Yang, W.; Zhang, Q. HNF1A-AS1 Regulates Cell Migration, Invasion and Glycolysis via Modulating miR-124/MYO6 in Colorectal Cancer Cells. Oncotargets Ther. 2020, 13, 1507–1518.
  95. Feng, Z.; Wang, B. Long non-coding RNA HNF1A-AS1 promotes cell viability and migration in human bladder cancer. Oncol. Lett. 2018, 15, 4535–4540.
  96. Gottesman, M.M. Mechanisms of cancer drug resistance. Annu. Rev. Med. 2002, 53, 615–627.
  97. Luo, X.; Wei, J.; Yang, F.-L.; Pang, X.-X.; Shi, F.; Wei, Y.-X.; Liao, B.-Y.; Wang, J.-L. Exosomal lncRNA HNF1A-AS1 affects cisplatin resistance in cervical cancer cells through regulating microRNA-34b/TUFT1 axis. Cancer Cell Int. 2019, 19, 323.
  98. Degli Esposti, D.; Hernandez-Vargas, H.; Voegele, C.; Fernandez-Jimenez, N.; Forey, N.; Bancel, B.; Le Calvez-Kelm, F.; McKay, J.; Merle, P.; Herceg, Z. Identification of novel long non-coding RNAs deregulated in hepatocellular carcinoma using RNA-sequencing. Oncotarget 2016, 7, 31862.
  99. Haberman, Y.; BenShoshan, M.; Di Segni, A.; Dexheimer, P.J.; Braun, T.; Weiss, B.; Walters, T.D.; Baldassano, R.N.; Noe, J.D.; Markowitz, J.; et al. Long ncRNA Landscape in the Ileum of Treatment-Naive Early-Onset Crohn Disease. Inflamm. Bowel. Dis. 2018, 24, 346–360.
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