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Review

Aberrant Regulation of mRNA m6A Modification in Cancer Development

by
Junyun Luo
,
Hui Liu
,
Siyu Luan
,
Chongsheng He
and
Zhaoyong Li
*
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Biology, Hunan University, Changsha 410082, China
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2018, 19(9), 2515; https://doi.org/10.3390/ijms19092515
Submission received: 23 July 2018 / Revised: 16 August 2018 / Accepted: 17 August 2018 / Published: 25 August 2018
(This article belongs to the Collection Regulation by Non-coding RNAs)
Browse Figure
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Abstract

:
N6-methyladenosine (m6A) is the most prevalent internal modification of eukaryotic messenger RNAs (mRNAs). The m6A modification in RNA can be catalyzed by methyltransferases, or removed by demethylases, which are termed m6A writers and erasers, respectively. Selective recognition and binding by distinct m6A reader proteins lead mRNA to divergent destinies. m6A has been reported to influence almost every stage of mRNA metabolism and to regulate multiple biological processes. Accumulating evidence strongly supports the correlation between aberrant cellular m6A level and cancer. We summarize here that deregulation of m6A modification, resulting from aberrant expression or function of m6A writers, erasers, readers or some other protein factors, is associated with carcinogenesis and cancer progression. Understanding the regulation and functional mechanism of mRNA m6A modification in cancer development may help in developing novel and efficient strategies for the diagnosis, prognosis and treatment of human cancers.

1. Introduction

Analogous to DNA and histone, epigenetic modification to RNA species has been well documented for several decades [1]. More than 100 types of chemical modifications have been identified in native cellular RNAs, including messenger RNAs (mRNAs), ribosomal RNAs (rRNAs), transfer RNAs (tRNAs), small nuclear RNAs (snRNAs) and small nucleolar RNAs (snoRNAs) [2]. N6-methyladenosine (m6A) is the most abundant modification in eukaryotic mRNAs [3]. Although first discovered in 1974 [4], m6A modification has gotten more attention recently since the development of high-throughput sequencing. Benefiting from advancements in techniques that combine m6A-specific methylated RNA immunoprecipitation with high-throughput sequencing, it is possible to locate m6A in the transcriptome [5,6,7]. m6A sites are especially enriched near stop codons, in 3′-untranslated regions (3′ UTRs), and within long internal exons of mRNAs with a consensus sequence of RRACH (R corresponds to G or A; A = m6A; H corresponds to A, C, or U) [5,6]. N6-methyladenosine influences almost every stage of mRNA metabolism, including RNA folding and structure [8,9], maturation [10,11], nuclear export [12,13,14], translation [15,16], and decay [17,18,19], as well as other RNA modifications, such as adenosine-to-inosine editing [20]. As the most common internal mRNA modification found in eukaryotes, m6A modification is widely implicated in multiple biological processes, such as circadian rhythm [13], adipogenesis [11], spermatogenesis [12,21], embryonic stem cell self-renewal and differentiation [22,23,24,25], cortical neurogenesis [26], and so on.
However, increasing evidence shows a correlation between aberrant cellular m6A level and cancer. Early in 1996, a direct relationship between increased m6A mRNA methyltransferase activity and cellular transformation was reported [27]. In 2012, it was observed that the m6A content varied significantly across several cancer cell lines, with relatively high levels in HepG2 and MCF7 cancer cell lines, but low levels in prostate cancer cell lines PC3 and PC9 [6], which indicates that cellular m6A levels of different cancer types are discrepant. More recently, some researchers have established an effective circulating tumor cell (CTC) capture system and developed a method by which DNA and RNA methylation (5-methyl-2′-deoxycytidine (5-mdC), 5-methylcytidine (5-mrC), and N6-methyladenosine (m6A)) could be detected by mass spectrometry in a single cell [28]. With this method, they discovered significant down-regulation of DNA 5-mdC and up-regulation of RNA 5-mrC and m6A in CTCs from the blood of lung cancer patients, which linked DNA and RNA methylation modification to the formation and development of cancer cells [28].
The effect of aberrant m6A level on cancer development has also been addressed. One recent study reported that m6A levels regulated the premature polyadenylation (pPA) that truncates the gene and affects carcinogenesis [29]. Tumor suppressor genes are frequently truncated by pPA in cancer, which leads their encoded products to be non-functional or dominant-negative. Some tumor suppressor genes, including MAGI3, LATS1, and BRCA1, undergo intronic pPA following large internal exons in breast cancer cells. One major cause is decreased m6A levels in these exons in pPA-activated breast cancer cells compared to untransformed mammary cells [29]. Multiple functions of RNA m6A methylation and their impact on cancer progression have been well reviewed elsewhere [30,31,32], and we focus here on how mRNA m6A modification is aberrantly regulated in cancers. We summarize the function and regulatory mechanism of mRNA m6A in carcinogenesis and cancer progression, which highlights m6A regulatory factors as potential targets for the diagnosis, prognosis and treatment of human cancers.

2. m6A “Writers”, “Erasers” and “Readers”

m6A RNA modification can be installed enzymatically by various methyltransferases, collectively termed m6A “writers”. The first identified human RNA m6A methyltransferase was METTL3. In 1997, a ~200-kDa methyltransferase complex exhibiting methyltransferase activity was isolated from HeLa cell nuclear extract, and a 70-kDa subunit containing the S-adenosylmethionine-binding site was identified [33]. Because of its molecular weight, this subunit was named MT-A70 (or METTL3). In 2014, METTL14 was discovered as another RNA methyltransferase, sharing 43% identity with METTL3 and forming a stable heterodimer core complex with it [34]. This METTL3–METTL14 complex functions in cellular m6A deposition on mammalian nuclear RNAs (Figure 1). Besides METTL3 and METTL14, Wilms’ tumor 1-associating protein (WTAP) has been identified as another component of the human m6A methyltransferase complex [34,35]. By interacting with METTL3 and METTL14, WTAP contributes to their localization into nuclear speckles [35]. Moreover, WTAP is necessary for the catalytic activity of m6A methyltransferase in vivo. Therefore, WTAP functions as a regulatory subunit in the m6A methyltransferase complex and promotes recruitment of the m6A methyltransferase complex to mRNA targets [35]. Recently, METTL16 was revealed to be another kind of human m6A methyltransferase that binds to pre-mRNAs and non-coding RNAs including the U6 snRNA [36].
Internal m6A modification in mammalian messenger and non-coding RNAs is dynamic and reversible. N6-methyladenosine in RNA can be removed by demethylases, which are termed m6A “erasers”. In 2011, fat mass and obesity-associated (FTO) protein, an obesity susceptibility factor [37], was revealed as the first RNA N6-methyladenine demethylase [38]. FTO had efficient oxidative demethylation activity to target the copious N6-methyladenosine residues in RNA in vitro and affect the amount of m6A in cellular RNA in vivo. Later, in 2013, ALKBH5 was discovered as another mammalian demethylase that catalyzes the removal of m6A modification on RNA in vitro and in vivo [12]. In addition, the demethylation activity of ALKBH5 significantly influences assembly of mRNA processing factors in nuclear speckles, mRNA export, and RNA metabolism.
Proteins that selectively bind m6A can be defined as m6A “readers” that exert regulatory functions by selective recognition of methylated RNA. The human YTH domain family 2 (YTHDF2) specifically binds m6A-containing RNA as a reader protein and accelerates the decay of m6A-modified transcripts [17]. However, YTHDF1 selectively recognizes m6A-modified mRNAs and promotes ribosome occupancy of these mRNAs [15]. By interacting with initiation factors, YTHDF1 facilitates translation initiation of its mRNA targets. Although YTHDF1 and YTHDF2 share a great number of common target mRNAs, YTHDF1 binds RNA earlier during the mRNA life cycle than YTHDF2 does. Therefore, YTHDF1-mediated translation enhancement increases translation efficiency in the cytoplasm, whereas the following YTHDF2-mediated degradation controls the lifetime of target transcripts [15]. It presents a dynamic and multi-dimensional mechanism of m6A modification in regulating gene expression. YTHDF3, another direct reader protein of m6A, promotes protein synthesis through cooperation with YTHDF1 and affects methylated mRNA degradation mediated by YTHDF2 [39]. Consequently, all three YTHDF proteins may act in a synergistic manner to influence foundational biological processes related to m6A modification. Nevertheless, as an m6A reader in the nucleus, YTHDC1, has been reported to regulate mRNA splicing [10]. By recruiting pre-mRNA splicing factor SFSF3 while blocking SRSF10 mRNA binding, YTHDC1 enhances exon inclusion of targeted mRNAs. YTHDC2, the final member of the YTH protein family, has been revealed to affect the translation efficiency and abundance of its target mRNAs [21].
Additionally, RNA binding proteins HNRNPA2B1 and eIF3 have also been identified as direct m6A readers [40,41] (Figure 1). HNRNPA2B1 binds a subset of primary miRNA transcripts in the nucleus, interacts with the DGCR8 protein, a component of the pri-miRNA microprocessor complex, and facilitates primary miRNA processing [40]. The levels of m6A within 5′ UTRs are selectively increased by diverse cellular stresses [41]. eIF3, a component of the 43S translation preinitiation complex, directly binds to m6A residues within the 5′ UTRs of mRNAs and promotes cap-independent translation [41]. Recently, insulin-like growth factor 2 mRNA-binding proteins 1, 2 and 3 (IGF2BP1/2/3) have been discovered as a new family of m6A readers that recognize and bind m6A by their KH domains [42].

3. Function of m6A Writers in Cancer Development

METTL3, the first identified S-adenosylmethionine-binding subunit of the RNA methyltransferase complex, has been identified to play critical roles in multiple cancers [43,44,45]. METTL3 has been reported to inhibit myeloid differentiation of normal hematopoietic and leukemia cells [43]. Moreover, m6A modulated by METTL3 promotes leukemogenesis. METTL3 mRNA and protein expression in human acute myeloid leukemia (AML) cells are significantly higher than in healthy hematopoietic stem/progenitor cells (HSPCs) or other types of tumor cells. Furthermore, depletion of METTL3 in human myeloid leukemia cell lines facilitates differentiation and apoptosis and delays leukemia development in recipient mice in vivo. Mechanistically, METTL3 catalyzes m6A formation and promotes the translation of specific mRNAs critical for the regulation of proliferation, survival, and differentiation, including c-MYC, BCL2 and PTEN. METTL3 depletion in AML cells reduces the translation of such transcripts, resulting in AKT activation, increased cell differentiation and apoptosis [43]. One recent study demonstrated a vital role of METTL3-regulated m6A modification in the maintenance and radioresistance of glioma stem-like cells [44]. METTL3 was upregulated in glioma stem-like cells over the matched differentiated glioma cells and its silencing suppressed tumor growth in vivo. SOX2, one of the glioma reprogramming factors [46], was methylated in its specific sites of mRNA 3′ UTR by METTL3. Together with further recruitment of HuR onto m6A-modified sites, SOX2 mRNA was stabilized. Consequently, SOX2 mediated the METTL3-dependent maintenance and radioresistance of glioma stem-like cells [44]. Another recent study reported that METTL3 was associated with chemo- and radioresistance in pancreatic cancer cells [45]. A sphere formation assay revealed that pancreatic cancer cells with METTL3 knockdown showed significantly lower self-renewal abilities than control cells. Moreover, METTL3 depletion enhanced chemo- and radiosensitivity of cancer cells, which suggests that METTL3 has an important role in the acquisition of resistance to anticancer drugs and irradiation [45].
Besides m6A methyltransferase activity, METTL3 has also been reported to interact with translation initiation machinery to promote translation of a subset of m6A containing mRNAs, independent of its catalytic activity or downstream m6A readers [47]. By recruiting eIF3 to the translation initiation complex in the cytoplasm, METTL3 enhanced translation of target mRNAs including two oncogenes, epidermal growth factor receptor (EGFR) and the Hippo pathway effector TAZ. Furthermore, METTL3 expression increased in lung adenocarcinoma, and it promoted growth, survival, and invasion of human lung cancer cells [47]. These findings shed light on a critical oncogenic role of METTL3 in carcinogenesis.
METTL14, another m6A writer protein, has also been linked to cancer development. In 2017, one study found that m6A modification decreased in hepatocellular carcinoma (HCC), especially in metastatic HCC, and METTL14 was responsible for the aberrant m6A modification in this kind of cancer [48]. It was also found that METTL14 knockdown raised the metastatic capacity of HCC, but METTL14 overexpression restrained invasiveness and metastasis in HCC. Mechanistically, METTL14-dependent m6A methylation promoted the recognition and binding of DGCR8 to pri-miR-126 and enhanced its processing to mature miR-126. Consequently, miR-126 mediated the suppressive effect of METTL14 in HCC metastasis [48]. However, another study showed that METTL3 was significantly upregulated in human HCC and high expression of METTL3 was associated with poor prognosis for HCC patients [49]. It was shown that depletion of METTL3 restrained HCC growth and metastasis both in vitro and in vivo, but overexpression of METTL3 enhanced HCC cell proliferation and migration, as well as tumor growth in vivo. SOCS2, a known tumor suppressor, was identified to be a downstream target of METTL3. METTL3 methylated SOCS2 mRNA and attenuated its stability by YTHDF2-dependent degradation pathway [49].
Recently, high expression of METTL14 was observed in acute myeloid leukemia (AML) cells with t(11q23), t(15;17), or t(8;21), as well as in hematopoietic stem/progenitor cells (HSPCs). However, expression of METTLl14 and m6A level decreased during myeloid differentiation of HSPCs and AML cells [50]. Moreover, METTL14 depletion inhibited AML cell proliferation or survival and promoted terminal myeloid differentiation of normal HSPCs and AML cells. Mechanistically, METTL14 plays a critical role in AML development and maintenance by directly methylating mRNA and regulating mRNA stability and translation. MYB and MYC, two known oncogenic transcription factors that contribute to AML development by inhibiting differentiation and promoting self-renewal of AML cells [51,52], are important targets of METTL14 in AML [50].

4. Function of m6A Erasers in Cancer Development

As the first identified RNA m6A eraser, FTO has been demonstrated to promote leukemic oncogene-mediated cell transformation and leukemogenesis [53]. FTO is activated by several leukemic oncoproteins, and therefore is highly expressed in several AML subtypes (e.g., t(11q23)/MLL-rearranged, t(15;17), FLT3-ITD, and/or NPM1-mutated AMLs). FTO not only promotes cell proliferation/transformation and inhibits apoptosis in vitro, but also significantly facilitates leukemogenesis in vivo. Furthermore, through negatively regulating a set of critical genes (e.g., ASB2 and RARA) in AML as RNA m6A demethylase, FTO plays an oncogenic role and inhibits all-trans-retinoic acid (ATRA)-mediated differentiation of leukemia cells [53]. The functional importance of FTO in tumor progression has also been revealed in lung squamous cell carcinoma (LUSC) [54]. MZF1-activated MYC expression has been reported to contribute to progression of lung adenocarcinoma [55]. FTO exerts its oncogenic function in LUSC by enhancing MZF1 expression, through reducing m6A levels and increasing the stability of MZF1 mRNA transcripts [54].
Recently, FTO was observed to be elevated in cervical squamous cell carcinoma (CSCC) tissue and promote the chemo-radiotherapy resistance of CSCC [56]. FTO positively regulates β-catenin expression by reducing m6A levels in its mRNA transcripts. Subsequently, excision repair cross-complementation group 1 (ERCC1), as a downstream effector of β-catenin, contributes to FTO/β-catenin-induced chemo-radiotherapy resistance in CSCC. Moreover, there is a positive correlation between FTO and β-catenin expression in human CSCC samples, and the combination of FTO and β-catenin confers better prognostic value for overall survival of CSCC than FTO alone [56]. Interestingly, one study links oncometabolite to m6A modification in cancer [57]. R-2-hydroxyglutarate (R-2HG), which is generated by mutant isocitrate dehydrogenase 1/2 (IDH1/2) and is regarded as an oncometabolite, also possesses anti-tumor effect in leukemia [57]. By directly binding and restraining the demethylase activity of FTO, R-2HG promotes overall m6A modification in R-2HG-sensitive leukemia cells. The stability of transcripts, such as MYC and CEBPA, is impaired by the R-2HG/FTO/m6A axis, likely by a YTHDF2-dependent degradation mechanism. Therefore, R-2HG displays anti-leukemia activity by suppressing FTO/m6A/MYC/CEBPA signaling, as well as relevant pathways [57].
ALKBH5-mediated demethylation of mRNA N6-methyladenosine has been linked to cancer stem cell phenotypes. The breast cancer stem cell (BCSC) phenotype is induced by hypoxia, which leads to a reduction in total RNA m6A by activating the expression of ALKBH5 in an HIF-dependent manner [58]. NANOG, a pluripotency factor functioning in the maintenance and specification of cancer stem cells, is demethylated by ALKBH5 at an m6A residue in the 3′ UTR. As a result, NANOG mRNA is stabilized, and upregulated NANOG contributes to the enhanced percentage of BCSCs under hypoxic conditions [58].
Additionally, ALKBH5 maintains tumorigenicity of glioblastoma stem-like cells (GSCs) [59]. ALKBH5 is required for GSC self-renewal and predicts poor survival of glioblastoma patients. Furthermore, ALKBH5 demethylates FOXM1 pre-mRNA and increases its stability by interaction with HuR [60]. Subsequently, upregulated FOXM1 mediates ALKBH5-dependent GSC proliferation, self-renewal, and tumorigenicity [59]. Recently, another study also reported that RNA m6A modification regulated the self-renewal and tumorigenesis of glioblastoma stem cells [61]. It was found that knockdown of METTL3 or METTL14 expression enhanced, but overexpression of METTL3 inhibited, GSC growth and self-renewal. Likewise, inhibition of the RNA demethylase FTO with its inhibitor MA2 reduced GSC-initiated tumor growth and prolonged the lifespan of GSC-grafted mice substantially [61].

5. Function of m6A Readers in Cancer Development

As an m6A reader, YTHDF2 can selectively recognize and bind to m6A sites to mediate mRNA degradation [17]. One study demonstrated that miR-145 could target the 3′ UTR of YTHDF2 mRNA and suppress the expression of YTHDF2 at the levels of mRNA and protein in hepatocellular cells, leading to reduced mRNA degradation and increased mRNA m6A levels [62]. Moreover, YTHDF2 expression detected by immunohistochemical staining showed that it was closely related to malignancy of HCC, which indicates that it may play an important oncogenic role in liver cancer progression [62]. As another cytoplasmic m6A reader, YTHDF1 has been reported to be associated with poor prognosis in patients with hepatocellular carcinoma [63]. Based on The Cancer Genome Atlas (TCGA) data, researchers found that YTHDF1 was significantly enhanced in HCC and was positively correlated with pathology stage. In addition, Kaplan-Meier analysis showed that higher YTHDF1 expression was associated with worse survival of HCC patients [63].
IGF2BPs (IGF2BP1/2/3) are a new family of m6A reader proteins that directly bind mRNA transcripts via the consensus GG(m6A)C sequence [42] (Figure 1). On the one hand, IGF2BPs can increase the stability of m6A-modified mRNAs in the nucleus by recruiting HuR and MATR3, two known mRNA stabilizers. On the other hand, IGF2BPs enhance the translation of m6A-containing mRNAs in the cytoplasm. Moreover, IGF2BPs play an oncogenic role in human cancer cells by their oncogenic transcript targets, such as MYC [42]. However, YTHDC2 and hnRNPA2B1, two other m6A reader proteins, have not been documented for their involvement in m6A dysfunction in cancer. In view of their confirmed oncogenic role in tumor [64,65,66], their regulatory function in m6A-related cancer progression is deducible, but further experimental verification is still required.

6. Other Protein Factors Involved in Regulation of m6A Modification in Cancer Development

In addition to m6A writers, erasers, and readers, several protein factors have also been identified to modulate m6A modification and correlate with cancer development. Zinc finger protein 217 (ZFP217) is a transcription factor that directly activates the transcription of core stem cell genes and regulates the pluripotency of embryonic stem cells and somatic cell reprogramming [67]. In addition, by interacting with METTL3 and eliminating its RNA methyltransferases activity, ZFP217 prevents the deposition of m6A at transcripts and enhances their stabilization, including mRNAs of core stem-cell genes Nanog, Sox2, Klf4, and c-Myc [67]. Considering the accumulating evidence that ZNF217 plays an essential role in tumor progression, metastasis, and chemoresistance [68,69], it is predictable that ZNF217-regulated m6A modification, possibly by interaction with METTL3, is relevant in human cancers. Recently, it was discovered that the oncoprotein hepatitis B X-interacting protein (HBXIP), whose aberrant expression drives the aggressiveness of breast cancer, releases the expression of METTL3 by repressing its inhibitor let-7 g [70]. Interestingly, METTL3 in return activates the expression of HBXIP through m6A modification. Therefore, mutual regulation between HBXIP and METTL3 promotes progression of breast cancer [70]. Another recent study revealed that SMAD2/3, members of the TGFβ signaling pathway, which is associated with tumor progression [71], promoted binding of the m6A methyltransferase complex to a subset of mRNA transcripts and caused their destabilization and rapid degradation [72]. Thus, the TGFβ pathway may be involved in cancer development by affecting m6A epigenetic modification. In sum, these protein factors may participate in cancer progression by regulating expression or function of m6A methyltransferases.

7. Conclusions

Multiple lines of evidence show that m6A modification of mRNA is deregulated in numerous cancers, and its role in cancers has been verified by both in vitro and in vivo studies. Clarifying the molecular mechanisms that mediate these m6A modification changes in RNA and identifying the aberrant expression of m6A regulatory factors in clinical biopsy specimens could contribute largely to early diagnosis of cancer, prediction of cancer prognosis, and provision of novel therapeutic approaches for cancer. We summarize here that not only m6A writers [43,44,48,49,50], erasers [53,54,56,57,58,59], and readers [42,62,63], but also other protein factors, including oncoprotein [70], transcription factor [67], and signal transduction factor [72], affect m6A abundance and function in various cancers (Table 1). Therefore, overexpression or depletion of these m6A-related factors may alter m6A modification in tumors and interfere with cancer progression.
Notably, as shown in Table 1, the majority of m6A regulatory factors play an oncogenic role in cancers, despite m6A writers and erasers performing opposite functions in m6A modification. As one striking example, both m6A writer METTL14 [50] and m6A eraser FTO [53] are found to be highly expressed in AMLs, even in the same subtype—as in t(11q23) and t(15;17)—and play critical roles in AML development. One reasonable interpretation of these paradoxical phenomena may be that the difference in their protein structures determines their substrate specificity [73,74]. By recognizing and targeting different mRNA targets, including oncogenes and tumor suppressors, m6A writers and erasers can exert an analogous function in the development of the same cancer type. Additionally, it cannot be overlooked that different reader proteins bind the m6A of mRNA targets and confer divergent or even opposite final status. Therefore, developing an effective therapeutic strategy for one cancer type should be based on an overall consideration of the m6A writers’ and erasers’ functions and downstream targets, as well as m6A readers’ binding to the targets.
Recently, inhibitors of m6A-modifying enzymes have also been explored and identified as changing cellular m6A abundance. For example, meclofenamic acid was found to be a highly selective inhibitor of FTO in vivo for competing on FTO binding to m6A-containing nucleic acid [75]. However, some drugs are suitable for only one specific type of cancer, but not for multiple cancers, because of the heterogeneity of cancer [76]. Consequently, more clinically applicable selective and powerful drugs targeting regulatory proteins of m6A are expected to be developed. Elucidating the regulatory mechanism of mRNA m6A modification in carcinogenesis and cancer progression would serve to develop m6A-related factors as valuable targets for the treatment of human cancers.

Author Contributions

J.L., H.L. and S.L. collected references and wrote the manuscript; C.H. and Z.L. revised and completed the final manuscript.

Acknowledgments

This work was financially supported by the National Natural Science Foundation of China (81772552, 81572714, 81372215) and the Fundamental Research Funds for the Central Universities of China (531107051117, 531107051157).

Conflicts of Interest

The authors declare no conflicts of interest.

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Ijms 19 02515 g001 550
Figure 1. The writer, eraser, and direct reader proteins of N6-methyladenosine (m6A). m6A modification is dynamically regulated by writers (METTL3 or METTL14) and erasers (fat mass and obesity-associated (FTO) or ALKBH5), both of which are localized primarily in the nucleus. In the nucleus, m6A can be recognized and directly bound by m6A readers YTHDC1, HNRNPA2B1, andIGF2BP1/2/3. In the cytoplasm, m6A can be recognized and directly bound by m6A readers YTHDF1/2/3, YTHDC2, eIF3, and IGF2BP1/2/3. Recognition and binding of m6A by different readers in the nucleus or cytoplasm mediate divergent biological functions. WTAP, Wilms’ tumor 1-associating protein.
Figure 1. The writer, eraser, and direct reader proteins of N6-methyladenosine (m6A). m6A modification is dynamically regulated by writers (METTL3 or METTL14) and erasers (fat mass and obesity-associated (FTO) or ALKBH5), both of which are localized primarily in the nucleus. In the nucleus, m6A can be recognized and directly bound by m6A readers YTHDC1, HNRNPA2B1, andIGF2BP1/2/3. In the cytoplasm, m6A can be recognized and directly bound by m6A readers YTHDF1/2/3, YTHDC2, eIF3, and IGF2BP1/2/3. Recognition and binding of m6A by different readers in the nucleus or cytoplasm mediate divergent biological functions. WTAP, Wilms’ tumor 1-associating protein.
Ijms 19 02515 g001
Table
Table 1. Function of m6A regulatory factors in various cancers.
Table 1. Function of m6A regulatory factors in various cancers.
TypeMoleculeCancerRoleFunctionReference
m6A writerMETTL3hepatocellular carcinomaoncogenicAttenuate SOCS2 mRNA stability [49]
METTL3gliomaoncogenicMethylate and stabilize SOX2 mRNA[44]
METTL3acute myeloid leukemiaoncogenicControl expression of c-Myc, Bcl-2 and PTEN[43]
METTL14acute myeloid leukemiaoncogenicRegulate mRNA stability and translation of MYB and MYC[50]
METTL14hepatocellular carcinomatumor suppressiveRegulate processing of miR-126 by DGCR8[48]
m6A eraserFTOacute myeloid leukemiaoncogenicTarget a set of critical genes including ASB2 and RARA[53]
FTOleukemiaoncogenicIncrease stability of Myc/CEBPA transcripts[57]
FTOcervical squamous cell carcinomaoncogenicPositively regulate β-catenin/ERCC1 axis[56]
FTOlung canceroncogenicDemethylate MZF1 mRNA and increase its stability[54]
ALKBH5breast canceroncogenicDemethylate NANOG and increase its mRNA level[58]
ALKBH5glioblastomaoncogenicDemethylate FOXM1 that promotes GSC tumorigenicity[59]
m6A readerYTHDF1hepatocellular carcinomaoncogenicAssociated with poor prognosis of HCC patients[63]
YTHDF2hepatocellular carcinomaoncogenicAssociated with malignancy of cancer [62]
IGF2BP1/2/3cervical cancer, liver canceroncogenicStabilize methylated mRNAs of oncogenic targets such as MYC[42]
Protein factorZFP217N/AoncogenicInteract with METTL3 and sequester it into an inactive complex[67]
SMAD2/3N/AN/APromote binding of m6A methyltransferase complex to mRNA transcripts[72]
HBXIP breast canceroncogenicUpregulate METTL3 by inhibiting let-7 g[70]

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Luo, J.; Liu, H.; Luan, S.; He, C.; Li, Z. Aberrant Regulation of mRNA m6A Modification in Cancer Development. Int. J. Mol. Sci. 2018, 19, 2515. https://doi.org/10.3390/ijms19092515

AMA Style

Luo J, Liu H, Luan S, He C, Li Z. Aberrant Regulation of mRNA m6A Modification in Cancer Development. International Journal of Molecular Sciences. 2018; 19(9):2515. https://doi.org/10.3390/ijms19092515

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Luo, Junyun, Hui Liu, Siyu Luan, Chongsheng He, and Zhaoyong Li. 2018. "Aberrant Regulation of mRNA m6A Modification in Cancer Development" International Journal of Molecular Sciences 19, no. 9: 2515. https://doi.org/10.3390/ijms19092515

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