Epi-miRNAs: Regulators of the Histone Modification Machinery in Human Cancer

Cancer is a leading cause of death and disability worldwide. Epigenetic deregulation is one of the most critical mechanisms in carcinogenesis and can be classified into effects on DNA methylation and histone modification. MicroRNAs are small noncoding RNAs involved in fine-tuning their target genes after transcription. Various microRNAs control the expression of histone modifiers and are involved in a variety of cancers. Therefore, overexpression or downregulation of microRNAs can alter cell fate and cause malignancies. In this review, we discuss the role of microRNAs in regulating the histone modification machinery in various cancers, with a focus on the histone-modifying enzymes such as acetylases, deacetylases, methyltransferases, demethylases, kinases, phosphatases, desumoylases, ubiquitinases, and deubiquitinases. Understanding of microRNA-related aberrations underlying histone modifiers in pathogenesis of different cancers can help identify novel therapeutic targets or early detection approaches that allow better management of patients or monitoring of treatment response.


Introduction
Epigenetics is defined as stable and heritable alterations in gene expression and cellular function without changes to the original DNA sequence and can still be passed on from generation to generation [1].
is term was first used to describe gene-environment interactions that lead to manifestations of various phenotypes during development. Epigenetic changes are perceived to be key contributors to cell differentiation and acquisition of different cell fates with the background of the same genome. DNA methylation, histone modification, and RNA modifications are crucial components of epigenetics [2][3][4].
DNA methylation is defined as the addition of methyl groups (CH 3 ) on cytosine residues of CpG islands, especially those located in the gene promoter region [2,5]. For instance, the promoter regions of microRNA (miR) 101-2, miR-126, miR-148a, miR-152, and miR-185-5p are hypomethylated in prostate cancer [6], and the promoter region of miR-200b is hypermethylated in the metastatic phase of the same disease, leading to increased and decreased gene expression [7].
Histone modification is a post-translational rearrangement of histone proteins driven by methylation, acetylation, phosphorylation, ubiquitylation, and sumoylation [8]. RNA modification and noncoding RNA-associated gene silencing are involved in epigenetics by DNA methylation and/or histone modifications in two ways: (1) changing the structure of RNA and interference with RNA and proteins interactions and (2) inciting subsequent events by altered RNA-binding proteins (RBPs) [4]. ese regulatory mechanisms can cause gene expression to be turned on or off [8]. Several studies have suggested that such modifications may play a role in inducing various disorders, most notably cancer [9]. Aberrant regulation of proteins or enzymes that regulate these modifications is a common feature in most cancers [9]. Among the multiple gene expression events regulated by these enzymes, the most pivotal genes controlling the cell cycle are refined into oncogenes or tumor suppressors [10].
MicroRNAs (miRNAs and miRs) are small noncoding RNAs with a length of approximately 22 nucleotides [11]. In the nucleus, they are first transcribed as 70 base-pair long double-stranded pri-miRNAs containing stem-loop structures [11]. en, they undergo a cascade of processes in which they are converted to pre-miRNAs and transmitted to the cytoplasm, where they are cleaved to form singlestranded mature miRNAs [11]. With the cooperation of the RNA-induced silencing complex (RISC), mature miRNAs can seek and bind to complementary sequences in the target mRNA [11]. Depending on the exact or imprecise miRNA-mRNA interactions, mRNA eradication or translational hindrance will occur [11].
Cancer development is a multistep process, and genetic alterations in every step are manifested by significant dysregulation of proteins involved in cell cycle regulation, which may have been triggered by miRNAs [11,12]. miRNAs can accomplish this by not only directly blocking the expression of the targeted genes but also by regulating the expression of epigenetic modifiers as well as histone methylases that play role in chromosomal structural changes [12,13]. Hence, microRNAs can also participate in regulating epigenetic mechanisms in cancer, and their abnormal expression profiles have been frequently indicated in malignancies.
is review will discuss histone modifications and the microRNA-mediated regulation of the histone modification machinery in cancer.

Alterations of Histone Modification in Cancer
Histones are lysine-arginine abundant proteins involved in chromosome condensation, consisting of four core types (H2A, H2B, H3, and H4) located in the bead of the nucleosome, along with two linker histones (H1/H5). e amino and carboxy termini of these proteins may undergo modifications, such as methylation, acetylation, phosphorylation, sumoylation, ubiquitination, and ADP-ribosylation, which are pivotal for transcriptional regulation. e addition of acetyl group on lysine residues of the H3 and H4 classes of histones results in a lightly packed chromosome structure and transcription activation [14]. Lysine residues can be mono-, di-, or trimethylated although arginine residues can only be mono-or dimethylated. Functioning like a doubleedged sword, histone methylation may lead to the development of either heterochromatin or euchromatin structures depending on factors such as the number of methyl groups, type of histone, and amino acid residues [15]. e heterochromatin formation that is followed by H3 three methylation at lysine 9 (i.e., H3K9me3) inclines towards transcriptional inactivation. However, histone H3 Lys-4 methylation (i.e., H3K4me) may lead to a transcriptional activation change [14]. Moreover, phosphorylation that occurs on serine residues, especially on H1 and H3 histones, can lead to gene expression induction. Ubiquitination usually takes place on H2A and H2B proteins and is correlated with activation although ADP-ribosylation is associated with chromosomal condensation [16]. e outcome of the ubiquitin-like modifier (SUMO) has been termed histone sumoylation and is related to transcription inactivation. Table 1 summarizes the above effects of different histone modifications and their impact on transcriptional regulation.
Given that histone modification affects gene transcription and appears early in tumorigenesis, considerable research has been carried out on the role of these alterations in malignancies. H4K16 hypoacetylation has been identified in breast, colon, lung, and liver cancers as well as in medulloblastomas [17,18]. is abatement in acetylation, together with H4K20me3 loss and co-occurrence in repetitive sequences with decreased DNA methylation and H4k20 trimethylation, has been reported in many cancers such as breast and lung cancer [17,18]. Besides lysine 20 and 16 H4, alterations of other lysine residues of this histone are prominent in malignancies. For instance, H4k5 and H4K8 hyperacetylation along with H4K12 deacetylation has been demonstrated in lung cancer [15]. As stated in a metaanalysis study, elevated levels of H3K4me3 and decreased levels of H3K4me2 are indicators of a poor outcome in cancer patients [19]. Other lysine residues of the H3 shift have been found to be elevated in tumorigenesis. For example, loss of H3K4me2, H3K18ac, H3K9ac, and H3K9me3 is related to lung cancer recurrence and poor prognosis [15]. ese modifications are located in promoters of transcribed genes and are essential for transcriptional suppression [20]. Moreover, H3K9me3 could serve as prognostic and staging estimation biomarkers in gastric cancer [21]. Loss of H2Bub1 is found in the development of numerous cancers as well as breast, lung, and colorectal cancer [22]. In addition, extensive phosphorylation of H2Bser32 has been shown in skin cancer cells [23].
All of these modifications are involved in malignancy induction by revising tumor suppressors or oncogene expression. H3 and H4 hypoacetylation and hypermethylation lead to p21WAF1 tumor suppressor inactivation [17]. Loss of H3K9ac, H3K4me2, and H3K9me3 has been linked to an increase in oncogene levels, such as MEIS1 and HOXA9 [21]. Increased and decreased methylation of H3K9 and H3K4, respectively, have been associated with p16INKA and p14ARF tumor suppressor gene reductions in some neoplasia [21].
Furthermore, dysregulation of histone-modifying enzymes in cancer and their distinct expression profile in tumor cells compared to normal cells have been identified in some studies [24]. For example, histone deacetylase (HDAC) reduction may be correlated with lung cancer promotion. However, HDAC overexpression in colon, prostate, and gastric cancers can result in blockage of tumor suppressor genes [15,25]. EZH2, an H3K27 trimethylation enzyme, raises in breast carcinoma [15]. A histone methyltransferase upregulation along with histone demethylase downregulation has been found in prostate tissues. Moreover, HDM (histone demethylase) high expression levels have been reported in the liver, while HDM and HMT are largely decreased in the brain. By contrast, elevated levels of HDMs have been found in prostate and brain malignant cells [26].

Regulation of miRNA Expression by Histone Modifiers
miRNAs are involved in the regulation of biological processes such as development, growth, differentiation, proliferation, and apoptosis [27]. Alterations in miRNA function have been reported in all diseases and conditions, markedly in cancer [27]. Furthermore, miRNA expression profiling can provide prognostic and treatment monitoring biomarkers, as well as indicators of recurrence [27]. ey can target cellular checkpoint genes and genes involved in mitosis division and apoptosis. For this reason, they are typically divided into two classes, onco MIRs and tumor suppressor MIRs [28].

Onco MIRs.
Onco MiRs (oncomir) switch tumor-linked operations, such as unlimited cell growth, transformation, and metastasis. miR-21 is an oncomir known to be elevated in many cancers and drives cell proliferation. A sort of H3K4 demethylase, known as RBP2, can decrease miR-21 levels followed by decreased H3K4 trimethylation of its promoter and could act as a novel treatment in chronic myeloid leukemia cells [29]. Overexpression of miR-224 oncomir is regulated by H3K9 and H3K14 acetylation in hepatocellular carcinoma [30]. e miR-155 promoter will alter heterochromatin as a result of H2A and H3 deacetylation carried out by BRCA1 and HDAC2, resulting in increased cell growth and proliferation [31].

Tumor
Suppressor miRs. miR-29 is known as a tumor suppressor gene because of its function in preventing cell growth and proliferation. H3K27 trimethylation is accomplished by recruiting YY1 and Ezh2. is change is related to the miR-29 promoter and could repress its expression in skeletal muscle cells. Aberrant downregulation of miR-29 by raised H3K27me3 is found in rhabdomyosarcoma [32]. Furthermore, induction of H3K27me3 and histone acetylation results in reduced levels of miR-31 [20]. miR-34a, a tumor suppressor gene governing apoptosis and cell cycle obstruction, can be arrested due to H3K27 trimethylation of its promoter by EZH2 in pancreatic ductal adenocarcinoma [33]. miR-125b has a tumor suppressor function in breast cancer, and its expression can be silenced through H3K9 and H3K27 trimethylation in breast cancer cell lines since miR-125b-1 promoter is located in a CpG island [34]. miR-30 family members classified as tumor suppressors are downregulated in a variety of malignancies. In esophageal squamous cell carcinoma cells, miR-30c expression is inactivated as a result of H2B and H4 histone deacetylation at the promoter region of miR-30c [35]. Downregulation of miR-15a, miR-16, and miR-29b in chronic lymphocytic leukemia is mediated by HDACs [36]. Other examples of these miRNAs are given in Table 2.

Epi-miRNAs and Histone Modification Machinery in Cancer
e epigenetic profile in numerous cancers is altered by the action of miRNAs [49,50]. ese small noncoding RNAs can target different enzymes involved in histone modifications. In the following sections, we discuss these miRNAs in more detail according to their enzyme targets.
ere are numerous studies demonstrating miRNA-mediated regulation of different histone acetyltransferases including EP300, PCAF, TIP60, and hCLOCK (Table 3). e polycistronic miR-106b-25 cluster, which consists of miR-106b, miR-93, and miR-25, is associated with proto-oncogenic functions and uncontrolled growth. As Zhou et al. suggested in their research, this oncoMIR cluster can target EP300, a histone acetyltransferase that modifies chromatin remodeling, cellular growth, and differentiation processes. Upregulation of the miR-106b-25 cluster in breast cancer leads to metastatic alterations by EP300 blockage [51]. PCAF or p300/CBPassociated factor is another histone acetyltransferase upregulated in prostate cancer cells, and its expression level is decreased through miR-17-5p binding [52]. miR-22, elevated in most cancers, can target and repress a lysine acetyltransferase named TIP60 [53]. Accordingly, miR-22 suppression may influence treatment in breast cancer cell lines by reducing metastasis [53]. hCLOCK, a target of miR-124, is significantly decreased in response to the elevated levels of miR-124 in a human colorectal cancer cell line known as LOVO cells [54].

miRNA-Mediated Regulation of Histone Deacetylases.
HDACs are classified into four classes including classes I-IV [55]. ere has been accumulating evidence of miRNA-mediated regulation of these enzymes (Table 4), and the following section describes these according to their classifications.   ). e upregulation of HDAC1 results in uncontrolled growth and cisplatin-resistant in ovarian cancer cells. miR-34a suppresses this process by targeting HDAC1 [56]. Moreover, an HDAC1 decrease through the action of miR-34a can overcome treatment resistance in breast cancer [67]. miR-145 is a tumor suppressor, and its inactivation can increase HDAC2 levels and lead to the development of hepatocellular carcinoma [57]. Kim et al. demonstrated that miR-326 inhibition may give rise to HDAC3 upregulation followed by a response to anticancer drugs in hepatoma and melanoma-related cell lines [58]. As demonstrated by Wang et al., the expression of miR-216b, which controls HDAC8, is downregulated in gastric adenocarcinoma [68]. (HDAC4, HDAC5, HDAC6, HDAC7, and HDAC9). Alterations in HDAC4 expression occur via several miRNAs and vary based on cancer type. Amodio et al. found that miR-29b/HDAC4 serves as an epigenetic loop in multiple myeloma and the induction of miR-29b expression could repress HDAC4 and result in cell survival and reduced malignancy in myeloma [59]. However, Ahmad et al. reported that induction in miR-10b levels leads to the tamoxifen-resistance phenotype due to loss of HDAC4 expression in ER-positive breast cancer cells [60]. Moreover, in another study carried out on fulvestrant-resistant breast cancer cells, it was found that miR-22 overexpression inhibits HDAC4 and promotes cell proliferation [61]. One observation has already drawn attention to the paradox in HDAC4 function in breast tumorigenesis since its suppression through miR-125a-5p inhibits tumor progression [62]. e downregulation of this miRNA, which targets HDAC5 in breast cancer cells, is related to the blockade of cancer progression [63]. Liu et al. found that the expression level of HDAC5 was reduced by binding of miR-589-5p to the 3' untranslated region (UTR) of HDAC5 in non-small-cell lung cancer (NSCLC) cells [64]. HDAC6 is downregulated via miR-221, which is upregulated in liver cancer cells [65]. Diminished levels of miR-489 induce metastatic processes of gastric cancer cells and block HDAC7 expression [66]. e levels of miR-34a may reflect the tumor-suppressive effect, and its transcription is abolished in cancer stem cells [67]. miR-34a targets HDAC7 and thereby contributes to the regulation of therapy resistance in breast cancer [67]. It has been shown that HDAC7-mediated deacetylation of a specific lysine residue of a heat shock protein, namely HSP70 K246, contributes to the augmentation of treatment resistance, in which miR-34a may exert a suppressive role through its downstream effectors HDAC7 [67]. miR-377 depression is found in oral squamous cell carcinoma, influencing the expression of HDAC9 and tumor invasion [69].

Class III Sir2-Like
Proteins (SIRT1, SIRT2, SIRT3, SIRT5, SIRT6, and SIRT7). SIRT is a family of histone deacetylase compromised seven proteins and divided into four classes. Class I includes SIRT1, SIRT2, and SIRT3. Class II consists of SIRT4. SIRT5 belongs to class III, and SIRT6 and SIRT7 are class IV members [80]. Being elevated in breast cancer, SIRT1 plays a significant role in this disorder [62]. Several miRNAs interact with SIRT1. miR-34a, a direct regulator of SIRT1, is decreased in breast cancer [62]. As  [72]. Reduced levels of miR-590-3p are associated with upregulation of SIRT1 followed by hyperacetylation of p53 and increased levels of BAX and p21, leading to malignant characteristics in breast cancer cells [73]. It has been shown that downregulation of miR-22 is accompanied by overexpression of SIRT1 in breast cancer tissues [74]. Downregulation of SIRT2 as a result of miR-150 augmentation has been observed in NSCLC cells, potentially serving as a survival element through blocking the AKT signaling pathway in this cell line [75]. SIRT3 is fine-tuned by miR-708-5p that is upregulated in pancreatic ductal adenocarcinoma [76]. Dang et al. confirmed that miR-299-3p, downregulated in hepatocellular carcinoma cells [77], exerts tumor-suppressive roles by modifying growth and metastasis through SIRT5 inactivation [77]. SIRT6 is a direct target of miR-186, and Ruan and colleagues demonstrated that miR-186 upregulation could serve as a treatment target in lung cancer [78]. miR-3666 inhibits breast cancer cell proliferation by targeting SIRT7. Also, overexpression of SIRT7 in response to downregulation of miR-3666 has been observed in NSCLC and breast cancer cells [79,81].
ere are two major types of histone methyltranferases termed histone lysine N-methyltransferases and histone arginine N-methyltransferases. e following sections discuss the miRNA-mediated regulation of both types.

miRNA-Mediated Regulation of Histone Lysine
Methyltransferases. Lysine methyletransferases (KMTs) are divided into groups based on the site of methyl group addition [82]. In this section, we discuss miRNA-mediated regulation of histone lysine methyltransferases considering their classification. e data summary is given in Table 5.
(6) SET8 (H4K20). SET8 is a histone methyltransferase that adds one methyl group on lysine 20 of H4. Its expression can be switched by miR-502, and it has oncogenic effects and contributes to cell growth and migration.
is oncogene expression can be increased due to reduced levels of miR-502 in many malignancies including breast cancer, ovarian cancer, small-cell lung cancer, colorectal cancer, non-Hodgkin's lymphoma, esophageal squamous cell carcinoma, clear cell renal cell carcinoma, and hepatocellular carcinoma [96,98,102,103]. For these reasons, it has been considered as a potential target for cancer therapy. Also, a single nucleotide polymorphism (SNP; rs16917496) located at the binding sequences of miR-502 may affect SET8 expression and has been associated with the risk of these malignancies [97, 99-101, 104, 124]. Moreover, this histone methyltransferase could be regulated with miR-7, and its suppression prevents cell invasion in breast cancer [105].
(7) EZH1 and EZH2 (H3K27). Elevation of KMT6B (EZH1) caused by miR-17-5p downregulation is related to erlotinib resistance in NSCLC [106]. miR-765 is another regulating element of EZH1, and its downregulation is associated with aggravation of breast cancer [107]. Additionally, a study by Hu J. et al. showed that miR-93 is a key regulator of EZH1 as well as JAK1, STAT3, AKT3, SOX4, and HMGA2 in breast cancer stem cells [108]. In a study of prostate cancer stem cells, Lai et al. reported miR-574-5p depletion along with EZH1 and REL increased levels [109].
Multiple microRNAs can alter EZH2 expression. Effects of miR-101 on EZH2 have been observed in various cancers [125], and downregulation of this microRNA and elevation of EZH2 have been found in NSCLC tumor tissues, prostate cancer, and renal cancer [110][111][112]. According to a study by Konno et al., the microRNA-101-EZH2/MCL-1/FOS axis may be a target for endometrial cancer treatment [113]. miR-26a as an apoptosis inducer is another regulator of EZH2, and its diminished levels of this miRNA have been found in lung cancer, rhabdomyosarcoma, and prostate cancer [114,116,117]. It plays a role in Burkitt lymphoma and prostate cancer prevention by targeting c-myc, a transcription factor of EZH2 [115,117], and is involved in nasopharyngeal carcinoma inhibition by mitigating cyclin D3, E2, CDK4, and CDK6 along with overexpression of the CDK inhibitors p14ARF and p21CIP1 [118]. miR-137 downregulation is related to EZH2 upregulation in hepatocellular cell carcinoma and miR-137 inhibits hepatocellular cell carcinoma progression by EZH2 suppression [119]. In addition, miR-124 manifests the same action on EZH2 in cancer cell lines [120]. Liu and co-workers demonstrated miR-138 deficiency can give rise to cellular metastasis via targeting VIM, ZEB2, and EZH2 in squamous cell carcinoma cell lines [121]. A study by Koumangoye et al. implicated EZH2 and HDAC3 as indirect targets of miR-31 in esophageal cancer cells as their upregulation was associated with raised levels of miR-31 by directly regulating SOX4, which then acts on EZH2 and HDAC3 [125]. miR-98 is a key regulator of EZH2 and, according to the investigation of Liu et al., treatment of ovarian cancer stem cells with an expression plasmid containing EZH2-targeted miR-98 blocked cell growth, and ameliorated cell cycle status via increasing p21CIPI/WAF1 and E2F1 tumor suppressors and downregulating c-Myc and CDK2/cyclin E complex proto-oncogenes [126].

miRNA-Mediated Regulation of Histone Arginine
Methyltransferases. Protein arginine methyltransferases (PRMTs) are involved in histone post-translational methylation [126], and multiple investigations have found miRNA-mediated regulation of these enzymes in various cancers (Table 6). For example, an investigation by Li et al. found that diminished miR-503 levels were associated with Ovarian cancer stem cells [126] PRMT1 elevation in hepatocellular carcinoma [127]. CARM1 elevation improves cell growth in colorectal malignancies. miR-195 is an antitumor element and increases radiosensitivity in colorectal cancer cells as a result of PRMT4/CARM1 targeting [128,129]. miR-424-5p is another regulator of CARM1. Wang and his colleagues indicated its low levels in NSCLC tissues. Also, they stated that high levels of miR-424-5p could suppress CARM1 followed by decreasing tumor development [130]. Upregulation of PRMT5 is related to the impaired expression of miR-92b and miR-96 in lymphoid cancer cell lines and leads to ST7 inactivation by H3R8 and H4R3 methylation [131]. miR-1266 overexpression appears to decrease PRMT5 levels and modify cellular growth and proliferation, thus suggesting its use as a novel therapeutic target in prostate cancer [132]. PRMT9 expression is shifted by direct binding of miR-543 to its 3ʹ-UTR and increased levels of this miRNA have been associated with downregulation of PRMT9 and osteosarcoma cell growth [133].

miRNA-Mediated Regulation of Histone Demethylases.
ere are multiple histone demethylase enzymes divided into lysine and arginine methyltransferase groups. Histone lysine demethylases are classified into KDM1-8 families [134]. miRNA-mediated regulation of histone demethylases in cancer is described in the following sections and summaries shown in Table 7.

KDM1 (LSD1)
. LSD1 is a histone demethylase, controlled by miR-137 in a negative feedback loop in endometrial cancer [135]. miR-302 has been shown to be downregulated in hepatocellular carcinoma cells, and this miRNA could decrease LSD1 (AOF2) levels resulting in drug sensitivity improvement and c-myc suppression [136]. By contrast, Bourguignon et al. reported miR-302a and miR-302b upregulation and AOF2 suppression in mouse tumors and human head and neck squamous cell carcinomas [137]. Likewise, miR-302a overexpression along with AOF2, BCRP, and permeability glycoprotein 1 decrease has been found in prostate cancer [138]. (FBXL10 and KDM2B). FBXL10 is a direct target of miR-146b, and downregulation of this miRNA in later stages of epithelial ovarian cancer has been linked to FBXL10 increase that, in turn, induces metastasis. However, in the early stage of the disease, miR-146b reduction results in overexpression of cyclin D1 and cell proliferation [139]. Hong and co-authors reported miR-448 overexpression in gastric cancer. is miRNA binds to KDM2B and suppresses its expression that results in myc induction [140]. KDM2B is upregulated in cervical cancer cell lines and downregulates miR-146a-5p expression that, in turn, increases c-myc levels [141].

KDM3 (JMJD1A).
JMJD1A is a direct target of miR-627, and its low expression is related to growth and differentiation inhibition [142]. LMP1 and LMP2A induce miR-155 upregulation followed by JMJD1A suppression in nasopharyngeal carcinoma cases with poor prognosis [143].
ere is a loop between JMJD1A, EZH2, and let-7c in NSCLC cells, and inhibition of JMJD1A can downregulate EZH2. EZH2 depletion causes the let-7c increase. However, let-7c binds to the 3'-UTR of JMJD1A and EZH2 and shifts their expression in a feedback loop, predisposing them to cancer phenotype amelioration [144]. EWS/Fli1 oncoprotein participates in miR-22 suppression that can regulate KDM3A (JMJD1A/JHDM2A) expression. Downregulation of KDM3A results in tumorigenic profile reduction in Ewing sarcoma [145].

KDM4 (JMJD2B and JMJD2C
). JMJD2B can be regulated by miR-491-5p, and its overexpression via miR-491-5p downregulation has been observed in ERα-positive breast cancers and cell lines. miR-491-5p upregulation results in cell cycle arrest and attenuates growth through inhibition of JMJD2B in the same cancer [146]. miR-491-5p carries out the same function in gastric cancer by binding to the 3'UTR of JMJD2B.
is miRNA is a tumor suppressor, and its downregulation has been used as a biomarker in this disease [147]. Yong et al. illustrated that circZMYM2 inhibits miR-335-5p expression in prostate cancer cells and tissues and induces prostate cancer development. Overexpression of miR-335-5p as a treatment can block JMJD2C expression and reduce prostate cancer progression [148]. (JARID1B and RBP2). Studies have shown that JARID1B levels are ameliorated by miR-137 [152].

KDM5
us, increased levels of JARID1B and reduced levels of miR-137 have been found in acute lymphoblastic leukemia cell lines, and increased miR-137 can prevent uncontrolled cell proliferation [152]. miR-363-3p is expressed as a result of HIF-2a induction, followed by p21 suppression and resulting in JARID1B elevation in melanoma [151]. JARID1B/KDM5B is also known to be regulated by miR-138, miR-381-3p, and miR-486-5p as observed in breast cancer [153]. Reference [154] RBP2 is a direct target of miR-212, and its miR-543 Osteosarcoma [133] 8 Journal of Oncology overexpression in response to downregulation of miR-212 has been found in gastric carcinogenesis and hepatocellular carcinoma [149,150]. miR-212 acts as a tumor suppressor, and its aberrant expression participates in the augmentation of a cell proliferation phenotype through induction of impaired RBP2 expression and downregulation of P21CIP1/ P27kip1 [149,150].

miRNA-Mediated Regulation of Histone Kinases.
ere are several clusters of kinases classified by kinase domain sequences similarity, biological function, and other criteria [158]. miRNA-mediated regulation of histone kinases is described below and summarized in Table 8.

AGC (RPS6KA4/MSK2, PRKCD, PRKCB, RSK2, and PRKDC).
Reduction of miR-517a is found in bladder cancer cell lines. It has a tumor-suppressive effect and can target RPS6KA4/MSK2 [159]. e PRKCD kinase can be regulated by many kinds of miRNAs. miR-181a acts as an oncogene, and its upregulation decreases the chemosensitivity of cervical squamous cell carcinoma via PRKCD inhibition [160,161]. In ovarian cancer tissues, miR-181c was found to be decreased and caused a PRKCD increase via binding to its 3'UTR [162]. As reported by Yao et al., PRKCD knockdown in A2780 cells resulted in cell cycle arrest in the G1 phase and metastasis inhibition [162]. However, in another study carried out by Zhao et al., miR-224 functioned as an oncogene targeting PRKCD and enhanced chemoresistance in ovarian papillary serous carcinoma [163]. e downregulation of miR-197-3p along with PRKCB overexpression in gastric cancer has been reported [164]. Low levels of miR-634 increase RSK2 in relation to cisplatin resistance in ovarian cancer [165]. miR-488-3p represses PRKDC and increases malignant melanoma cell sensitivity to cisplatin [166].

Nonreceptor Tyrosine Kinase (JAK2)
. JAK2 is one of the most important kinases involved in histone regulation and the key member of the JAK2/STAT3 signaling pathway recruited in inflammation and apoptosis [218]. e level of JAK2 is regulated by a variety of miRNAs. e miR-543 expression serves as a tumor suppressor and prevents cell proliferation by targeting JAK2 and STAT3 in hepatocellular carcinoma [167]. Low levels of miR-216a and high levels of JAK2 in pancreatic cancer were reported in two distinct studies [168,169]. JAK2, BCl-2, and surviving are direct targets of miR-204 in breast cancer, and the opposite expression pattern of miR-204-JAK2 has been reported in  miR-26a Hepatocellular carcinoma [217] NSCLC [170,171]. Furthermore, miR-204 can be used as a prognostic marker in these cancers [170,171]. Several studies reported the downregulation of miR-375 in gastric cancer and its function in inhibiting tumor development by suppressing JAK2 [172,173]. miR-135a is another regulator of JAK2 in different cancers such as lymphoma and renal and gastric carcinoma and can influence apoptotic genes as well as Bcl-x and Bcl-2 [174][175][176].

Tyrosine Kinase-Like (LIMK2).
LIMK2 plays an oncogenic role in bladder cancer and can be decreased by miR-135a [183]. Family (NEK6, AURKA, and BUB1). miR-23 can target NEK6, the enzyme that negatively regulates p53. e natural substance berberine plays a role in hepatocellular carcinoma treatment by activating this signal [184]. In another study, miR-26 was documented as a modulator of NEK6 in Marek's disease lymphoma and suppressed cell proliferation [185]. NEK6 is an oncogene and a direct target of miR-506-3p in retinoblastoma [186]. miR-124-3p was found to be decreased in bladder cancer tissues and cell lines and glioblastoma, and its downregulation led to AURKA increase [187,188]. In NSCLC, miR-32 targets AURKA and causes p53 inhibition [189]. miR-137 can suppress AURKA expression and prevent drug resistance in multiple myeloma [190]. let-7 is another modulator of AURKA that is downregulated in hepatocellular cancer [191]. Diminished levels of miR-490 have been found in hepatocellular carcinoma, and AURKA as an established target of miR-490 was elevated [192]. Gomaa and colleagues found a relationship between miR-4715-3p downregulation caused by methylation and AURKA overexpression in gastrointestinal cancers that were attenuated by 5-Aza-2'deoxycytidine, a demethylation element [193]. Downregulation of miR-490-5p and miR-145-3p along with an increase in BUB1 was found in hepatocellular carcinoma and prostate cancer, respectively, leading to cancer cell invasion [194,195].

Other Kinases
(1) CAMK (DAPK3, CHEK1, CHEK2, and AMPK). DAPK3 is a p53-activating kinase and a direct target of miR-1307, which is overexpressed in chemoresistant ovarian cancer cell lines [205]. CHEK2 can be regulated by miR-191 in osteosarcoma, and miR-191 provokes cell growth [196]. miR-182-5p overexpression promotes CHEK2 suppression and is involved in breast cancer [197]. CHEK1 is controlled by several miRNAs, and its alteration functions a double-edged sword in different malignancies. Downregulation of miR-195 in NSCLC is correlated with augmentation of CHEK1, which is an indication of poor survival [198]. However, downregulation of miR-195 in colon cancer cell lines can suppress the viability of cancer 5-FU-resistant cells by increasing CHEK1 and might be considered as a treatment in colon cancer [199]. miR-497 is another regulator of CHEK1 in hepatocellular carcinoma [200]. miR-145 and miR-424 downregulation together with CHEK1 upregulation were found in bladder cancer and cervical cancer, respectively [201,202]. miR-15 can increase breast cancer cells irradiation by targeting CHEK1 [203]. p53 induces miR-16 and miR-26a expression, and they inhibit CHEK1 expression leading to enhanced apoptosis and better survival in breast and prostate cancers [204]. miR-451 overexpression hampers AMPK and promotes mTOR and FCN1 expression in colorectal cancers leading to proliferation induction [206]. A similar result was found with exogenous expression of miR-25-5p [207]. miR-101 and miR-34 are other regulators of AMPK, and an increase in their expression is associated with proliferation arrest and initiation of apoptosis in breast and prostate cancer, respectively [208,209].
showed that miR-134 suppression led to augmentation of PAK2 followed by paclitaxel resistance in human ovarian cancer cells [215]. In addition, CCHE1 inhibited miR-922, which, in turn, leads to an incline in PAK2 and participates in tumorigenesis of oral squamous cell carcinoma development [216], and miR-26a halted cancer invasion by restricting PAK2 in hepatocellular carcinomas [217].

miRNA-Mediated Regulation of Histone Phosphatases.
e main groups of protein phosphatases are sorted considering the structural fold of the catalytic domain [220], and miRNA-mediated regulations of these are summarized in Table 9.

HAD (EYA1 and EYA2).
e apoptosis activator miR-101 can repress EYA1 and is diminished in breast cancer [227]. miR-562 is another modulator of EYA1, and its downregulation has been found in sporadic Wilms' tumor [228]. miR-338 and miR-30a are EYA2 regulators, and their downregulation increases EYA2 expression in breast cancer, and its reduction and epidermal growth factor receptor (EGFR) downregulation have been associated with lung metastasis [229,230]. Furthermore, miR-30a overexpression was found to reduce EYA2 and attenuate cell metastasis in lung adenocarcinoma [231]. e expression of miR-219a-5p and miR-338-3p were shown to be diminished in osteosarcoma and cervical cancer, respectively, both targeting EYA2 [232,233]. EYA3, a direct target of miR-708, was upregulated in Ewing sarcoma, promoting chemoresistance [234]. 4.6.4. CC1 (DUSP1). DUSP1 is controlled by various miRNAs. In osteosarcoma, miR-34a targets DUSP1, and its repression is related to elevated levels of Bax and E-cadherin, along with diminished levels of Bcl-2, cyclin E, cyclin D1, and β-catenin [235]. Upregulation of miR-202-3p downregulates DUSP1 and provokes tumor development in gastric neuroendocrine neoplasms [236]. Various studies revealed that miR-324 and miR-101 function in DUSP1 targeting in hepatocellular carcinoma, and their upregulation impedes metastasis and promotes apoptosis, suggesting these as potential novel treatment targets [237,238].

miRNA-Mediated Regulation of Histone Desumoylation.
SENP1 is one of the most important desumoylation proteins modulated by various miRNAs (Table 10). SENP1 can be inactivated by multiple miRNAs. In lung cancer samples and cell lines, reduction of miR-138 along with SENP1 increase has been identified. miR-138 overexpression can elevate radiosensitivity by SENP1 blockage leading to increased apoptosis [239]. miR-133-3p and miR-186 are the regulators of SENP1 in colorectal and renal cell carcinoma, respectively. eir downregulation raises expression of the SENP1 oncogene in these cancers followed by accelerated proliferation [240,241]. In prostate cancer, miR-145 loses its tumor suppressor activity, and this leads to increased SENP1expression. In addition, CDX2 can target miR-145-5p and decrease metastasis [242,243].

miRNA-Mediated Regulation of Histone Ubiquitinations.
RBX1, RNF8, HUWE1, and UHRF1 are histone ubiquitinating enzymes involved in different malignancies. Below, we summarize the miRNA-mediated effects on the regulation of these enzymes (Table 11). RBX1 has been shown to be decreased by miR-378 and miR-194 in lung and gastric cancer, and this suppresses proliferation and metastasis [244,245]. Cheng et al. revealed that miR-542-5p targets HUWE1 and impedes osteosarcoma development [246]. RNF8 is another histone lysine ubiquitinase. miR-214 upregulation has been associated with RNF8 downregulation and provokes chromosomal instability in ovarian cancer cells [247]. Overexpression of miR-214 and miR-622 in breast cancer prevents cell proliferation by targeting RNF8 [248,249]. Several miRNAs can control UHRF1 expression in different neoplasia. For example, low levels of miR-145 and miR-124 have been linked to increased levels of UHRF1 in bladder cancer cell lines and accelerated cell aggressiveness [201,250,251]. miR-9 and miR-202 serve as tumor suppressors and attenuate cell migration through UHRF1 blockage [252,253]. Moreover, Goto et al. 12 Journal of Oncology demonstrated the antitumor function of miR-101 in renal cell carcinoma through the inactivation of UHRF1 [254].

Conclusions and Future Prospects
With due attention to the high cancer mortality rate, early diagnosis and initiation of appropriate therapeutics are urgently needed. To further these objectives, it is crucial to increase our understanding of the mechanisms and pathways involved in malignancy progression and improvement. e histone-modifying enzymes that catalyze the remodeling of chromatin structures play a major role in cancer biology. In this review, we discussed miRNAs that interact with a complex array of histone modifiers and reviewed the effects of their aberrant expression in various cancers. ese alterations impact the fluctuation of multiple cancer cell properties such as drug sensitivity, drug resistance, proliferation, apoptosis, and malignancy trajectories. Hence, recognition of these small noncoding RNAs is imperative for the early diagnosis of cancer and may lead to the identification of new biomarker tests to facilitate earlier diagnosis and treatment than is currently possible for the best outcomes.

Data Availability
ere are no raw data associated with this review article.

Ethical Approval
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Consent
Not applicable.

Disclosure
Deniz Mortazavi and Behnoush Sohrabi are co-first authors.   Journal of Oncology 13 Conflicts of Interest e authors declare that they have no conflicts of interest.

Authors' Contributions
e authors Deniz Mortazavi and Behnoush Sohrab were contributed equally to this work.