The YTH Domain Family of N6-Methyladenosine “Readers” in the Diagnosis and Prognosis of Colonic Adenocarcinoma

Xu, Dian; Shao, Jun; Song, Huan; Wang, Jianming

doi:https://doi.org/10.1155/2020/9502560

BioMed Research International

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Ethical Approval Consent Disclosure Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 9502560 | https://doi.org/10.1155/2020/9502560

The YTH Domain Family of N6-Methyladenosine “Readers” in the Diagnosis and Prognosis of Colonic Adenocarcinoma

Dian Xu,¹Jun Shao,²Huan Song,¹and Jianming Wang¹

Academic Editor: Ferdinando Chiaradonna

Received10 Jan 2020

Revised06 May 2020

Accepted07 May 2020

Published30 May 2020

Abstract

To profile the landscape of methylation N⁶ adenosine (m⁶A) RNA regulators in colonic adenocarcinoma (COAD) and to explore potential diagnostic and prognostic biomarkers, we assessed the differential expression patterns of m⁶A RNA methylation regulators between 418 COAD patients and 41 controls based on profiling from The Cancer Genome Atlas (TCGA) database. We plotted the receiver operating characteristic (ROC) curves and calculated the area under the curve (AUC) values to estimate the discrimination ability. The relationship between the expression of m⁶A RNA methylation regulators and clinicopathological characteristics was explored. Kaplan-Meier plotter, log-rank test, and Cox regression were used and a nomogram was created to explore the prognostic significance of m⁶A-related genes in overall survival at the mRNA level. Pathway analysis was performed by gene set enrichment analysis (GSEA) using TCGA dataset, and a coexpression network was built based on the STRING database. We observed that YTHDF1, METTL3, and KIAA1429 were significantly upregulated, while YTHDF3, YTHDC2, METTL14, and ALKBH5 were significantly downregulated in COAD samples compared to normal samples. YTHDF1 had the highest diagnostic value. Low expression of YTHDF3 predicted a poor survival rate in COAD patients. YTHDC2 was related to sex and showed a downward trend as clinical stage increased. Our results indicate that the YT521-B homology (YTH) domain family (“readers”), especially YTHDF1, YTHDF3, and YTHDC2, might play a significant role in the detection, progression, and prognosis of COAD, indicating that they are promising cancer biomarkers.

1. Introduction

Colon cancer is the third most common cancer and the second leading cause of cancer-related death worldwide [1]. Colonic adenocarcinoma (COAD) is the typical type that accounts for 98% of new cases [2]. Despite advances in diagnosis and treatment [3], the prognosis of patients remains poor. Chemotherapy has shown significant value, but surgery is the only method of curative treatment. Thus, it is crucial to discover novel diagnostic and prognostic biomarkers for COAD.

Epigenetic modification has gained increasing attention in research on carcinogenesis and progression. Methylation is a common epigenetic trait and a simple biochemical process—it is the transfer of four atoms, one carbon atom and three hydrogen atoms (CH3), from one substance to another [4]. The N6-methyladenosine (m⁶A) modification of mRNA/lncRNA is the most common RNA methylation, and it can regulate cell fate determination, self-renewal, and cancer development, indicating it as a promising therapeutic target for cancer [5]. Three major types of enzymes participate in m⁶A methylation: “writers,” “erasers,” and “readers.” “Writers” mainly include METTL3, METTL14, KIAA1429, and WTAP. METTL3 and METTL14 form a structure with other enzymes (e.g., WTAP) to methylate the sixth N of adenosine during transcription from DNA to RNA [6]. The m⁶A-modified bases can be demethylated under the action of "erasers" enzymes, such as FTO and ALKBH5, making RNA methylation a reversible reaction [7]. These methylated RNA base sites finally require specific enzymes ("readers") to recognize. YTHDF1, YTHDF2, and YTHDF3 are primary members of the "readers" family, devoted to recognizing bases that undergo m⁶A methylation, participating in downstream translation, mRNA degradation, and accelerating the rate at which mRNA leaves the nucleus [8].

Aberrant expression of m⁶A writers, erasers, or readers can lead to the deregulation of m⁶A modification, thus triggering the abnormal translation of specific mRNAs and promoting or inhibiting carcinogenesis and cancer progression [9]. Accumulative evidence has supported the correlation between aberrant cellular m⁶A and human cancers [10]. For example, the overexpression of YTHDF1 is related to poor prognosis in patients with liver cancer [11]; downregulation of ALKBH5 in MDA-MB-231 human breast cancer cells can lead to a decrease in the number of breast cancer stem cells, resulting in a significant reduction in tumorigenic capacity [12].

Although traditional prognostic factors for COAD, such as age, tumor stage, surgical margins, and tumor grade, have produced significant improvements in predicting patient clinical outcomes [13], their limitations in distinguishing the prognostic value of molecular heterogeneity should not be ignored. With deepening research on RNA methylation regulators, the roles of m⁶A in diagnosis and treatment have gradually become valued. This study is aimed at profiling the landscape of m⁶A RNA methylation regulators in COAD and at exploring their potential value as diagnostic and prognostic biomarkers.

2. Materials and Methods

2.1. Data Processing

We downloaded the expression data and clinicopathological data of 418 COAD patients and 41 controls after the deletion of missing records from TCGA database (https://tcga-data.nci.nih.gov/tcga/) [14]. Age at diagnosis, sex, follow-up days, and clinical data were retrospectively extracted. All patients were staged using the 2009 TNM classification system recommended by the American Joint Committee on Cancer. We used the edgeR package to normalize the expression data.

2.2. Portraying the Landscape of m⁶A RNA Methylation Regulator Expression

The expression levels of six m⁶A RNA methylation regulators between tumor and normal tissues were compared using the -test. The expression pattern of m⁶A RNA methylation regulators in COAD samples was denoted by the Pearson correlation matrix, and a correlation coefficient () was calculated. We plotted the ROC curve and calculated the area under the curve (AUC) to estimate the discrimination ability. The m⁶A RNA methylation regulators and clinicopathological features were analyzed using the -test or one-way ANOVA.

2.3. Survival Analysis

A total of 418 patients were followed, with a maximum follow-up period of 4502 days. The median survival time was 670.5 days. All patients had no chemotherapy history and underwent the same type of radical surgery and postoperative adjuvant chemotherapy. The overall survival (OS) was calculated from the date of diagnosis to the date of death. We categorized the expression of m⁶A-related mRNA into two groups using the lower quartile as the cutoff point. Kaplan-Meier analysis was used to portray the survival curves of m⁶A RNA methylation regulators. The log-rank test was used to compare the survival distributions between groups. We performed univariate and multivariate analyses to determine the independent prognostic factors using the Cox proportional hazard model. A nomogram was generated based on the significant prognostic factors in the Cox regression model to predict the 1-year, 3-year, and 5-year survival of COAD patients.

2.4. Biological Function Analysis

We further used gene data in TCGA database to search for pathways related to YTHDF1, YTHDF3, and YTHDC2 by gene set enrichment analysis (GSEA) using GSEA v2.2.2 software (http://www.broadinstitute.org/gsea). GSEA revealed significant differences in the enrichment of genes in the MSigDB Collection (c2.cp.kegg. v7.2. symbols) [15]. The high- and low-expression phenotype groups were divided according to the lower quartile expression level of candidate genes. Gene set permutations were performed 1000 times for each analysis. The expression of selected genes was used as a phenotype label. We selected the most significantly enriched signal pathway using the criterion of NOM value < 0.05, FDR value < 0.25, and high normalized enrichment score (NES). The Retrieval of Interacting Genes (STRING v10) (http://string-db.org/) tool was used to analyze the interactive relationships to construct a protein-protein interaction (PPI) network. Experimentally validated interactions with a combined were regarded as significant. We also selected the YTHDF1, YTHDF3, and YTHDC2 modules and constructed a PPI network of these selected m⁶A RNA regulators.

2.5. Statistical Analysis

A comparison of normalized data between two groups was conducted using -test or Mann-Whitney test by GraphPad Prism 7 (GraphPad Software, La Jolla, CA). Comparisons among multiple groups were performed using one-way ANOVA. Other analyses were visualized using R software (v.3.4.3). The significant level was set at 0.05.

3. Results

3.1. The Landscape of m⁶A RNA Methylation Regulators in COAD

A total of 418 COAD cases and 41 normal controls were included in the analysis. We compared the expression of 11 m⁶A RNA methylation regulators (YTHDF1, YTHDF2, YTHDF3, YTHDC1, YTHDC2, METTL3, METTL14, WTAP, KIAA1429, ALKBH5, and FTO). As shown in Figure 1(a), YTHDF1 (), METTL3 (), and KIAA1429 () were significantly upregulated, while YTHDF3 (), YTHDC2 (), METTL14 (), and ALKBH5 () were significantly downregulated in COAD samples compared to normal samples. No significant difference was observed for YTHDF2 (), YTHDC1 (), WTAP (), and FTO ().

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Figure 1

The landscape of m⁶A RNA methylation regulators in COAD. (a) The expression level of m⁶A RNA methylation regulators in cancer and normal tissues. ns: ; : ; : ; : . (b) The Pearson correlation matrix among 11 m⁶A modification regulators in COAD. The correlation coefficient is shown in each grid with different colors. The redder the color is, the higher the correlation coefficient; the bluer the color is, the lower the correlation coefficient. (c) ROC curves of seven differentially expressed m⁶A RNA methylation regulators. Each curve represents a candidate gene, and the AUC is shown at the bottom right.

Figure 1(b) shows the clustering of different genes and their correlation coefficients in COAD. YTHDF3 and KIAA1429 were the most positively correlated (). We also found a positive correlation in the cluster of METTL14, YTHDC1, YTHDC2, and YTHDF2, with correlation coefficients ranging from 0.4 to 0.6.

The ROC curves of 7 differentially expressed genes (YTHDF1, YTHDF3, YTHDC2, METTL3, METTL14, KIAA1429, and ALKBH5) are plotted in Figure 1(c). YTHDF1 had the highest AUC value (AUC: 0.974; 95% CI: 0.957-0.991), demonstrating the high sensitivity and specificity of YTHDF1 for COAD diagnosis.

3.2. m⁶A RNA Methylation Regulators and Clinicopathological Features

Compared to younger patients, patients older than 65 years had a lower expression level of YTHDC1 () and a higher expression level of ALKBH5 () (Figure 2(a)). YTHDC2 () was highly expressed in female patients (Figure 2(b)). Clinical stage was associated with YTHDF1 (Figure 3(a), ), YTHDC2 (Figure 3(e), ), METTL14 (Figure 3(g), ), and ALKBH5 (Figure 3(j), ) expression. YTHDC2 and METTL14 showed a significant downward trend with increasing clinical stage.

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3.3. Prognostic Value of m⁶A RNA Methylation Regulators

We used the lower quartile as the cutoff point to portray the survival curves of each m⁶A RNA methylation regulator. As shown in Figure 4, patients with the upregulated expression level of YTHDF2 and YTHDF3 had a better 5-year OS, with HR (95% CI) values of 0.564 (0.362–0.88) and 0.553 (0.358–0.854), respectively. Patients with higher T stage (HR: 3.409; 95% CI: 1.377-8.435; ), M stage (HR: 3.529; 95% CI: 2.265-5.501; ), and N stage (HR: 4.578; 95% CI: 2.907–7.209; ) had a lower survival rate than patients with lower stages. We then performed a multivariate Cox regression analysis based on the selected indicators in the univariate Cox regression model (Figure 5) using the stepwise forward method. YTHDF3, together with age, N stage, and M stage, was an independent prognostic factor for COAD (Table 1).

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Figure 5

Cox regression analyses of the m⁶A RNA methylation regulators and clinicopathological factors in the 5-year overall survival of COAD. The horizontal axis shows the hazard ratio, and the vertical axis shows the predictive factors. M_stage: M1 vs. M0. N_stage: N2 vs. N0 or N1. Prior_malignancy: yes vs. no. Treatment_type: surgery vs. other. Clinical_stage: III or IV vs. I or II. Sex: male vs. female. Age: ≥65 vs. <65. All m⁶A RNA methylation regulators: high expression level vs. low expression level, where the cutoff value was the lower quartile of each regulator.

3.4. Nomogram to Predict the Survival of COAD

Data on YTHDF3 expression, age, and clinical stages from TCGA dataset were used to establish a prognostic nomogram predicting overall survival based on the stepwise Cox regression model. Total score was obtained by adding up the individual contributions of the corresponding covariates on the points scale; the total score was used to predict 1-year, 3-year, and 5-year related survival probabilities (Figure 6).

3.5. GSEA Identified Related Signaling Pathways

Considering the critical associations of YTHDF1 with diagnosis, YTHDF3 with prognosis, and YTHDC2 with clinicopathological features observed by the above analysis, we further used the GSEA approach to explore the potential biological processes related to these genes. YTHDF1 mainly participates in basal transcription factors and spliceosomes (Supplementary Figure S1A and B). YTHDF3 is involved in ubiquitin-mediated proteolysis and the TGF-β signaling pathway (Supplementary Figure S1C and D). YTHDC2 is enriched in pathways of ubiquitin-mediated proteolysis, long-term potentiation, and prostate cancer (Supplementary Figure S1E, F, and G).

3.6. PPI Network Construction

Based on the STRING database, a coexpression network was constructed to explore interactions between m⁶A RNA methylation regulators (Supplementary Figure S2). We found that the writers (WTAP, KIAA1429, METTL3, and METTL14) closely interacted with each other (Supplementary Figure S2A). Further, we explored three module networks of selected m⁶A regulators (YTHDF1, YTHDF3, and YTHDC2) and broader genes. YTHDF1 was firmly related to YTHDF3 and shared many interacting proteins. Moreover, the writers (WTAP, KIAA1429, METTL3, and METTL14) also played essential roles in this network (Supplementary Figure S2B). In addition, many other genes were involved in forming the network, showing ample room for exploration.

4. Discussion

COAD is one of the most popular malignant gastrointestinal tract tumors and the second leading cause of cancer-related death in adults in Western countries [16]. During the past decades, many efforts have been made to search for biomarkers of COAD. Studies have shown the diagnostic value of DCTN1, DCTN2, and DCTN4 [17] and the prognostic role of LAYN [18], KCNQ1OT1 [19], and PYK2 [20] in COAD, but with limited sample size or inconsistent results. In this study, we analyzed the expression patterns of m⁶A RNA methylation regulators in COAD and their relationship with clinical features by using cohort data from TCGA. Most m⁶A-related proteins were dysregulated in COAD samples, and some were associated with clinical features. Among them, YTHDF1 had the highest diagnostic value for COAD. Survival analysis confirmed that high expression levels of YTHDF2 and YTHDF3 predicted a favorable prognosis. Moreover, YTHDF3 expression levels were independent prognostic factors of 5-year overall survival in COAD patients. YTHDC2 was highly expressed in female patients and showed a significant relationship with tumor progression. YTHDC1 was typically upregulated in younger patients. These results underscore the significant roles of the YTH domain family of readers, especially YTHDF1, YTHDF3, and YTHDC2, in the detection, progression, and prognosis of COAD.

In this study, we explored the roles of the YTH domain family of readers in COAD. m⁶A exerts many of its functions through reader proteins in the cytoplasm and nucleus that selectively bind to m⁶A-containing transcripts [21]. The "readers" are the bridge between "writers" and "erasers", and the ability of "readers" to block the accessibility of RNA demethylase may be critical to determining the m⁶A status of target transcripts [10], which may explain the critical roles of the YTH family in COAD. YTH domain family proteins include YTHDF1, YTHDF2, and YTHDF3 in the cytoplasm and YTHDC1 and YTHDC2 in the nucleus [22, 23]. YTHDF1 and YTHDF3 work in concert to affect the translation of m⁶A-containing mRNAs, YTHDF2 expedites mRNA decay, YTHDC1 affects the nuclear processing of its targets, and YTHDC2 selectively binds m⁶A at its consensus motif and enhances the translation efficiency of its targets and decreases their mRNA abundance [24–26]. Consistent with our results, Bai et al. reported that YTHDF1 could regulate tumorigenicity and cancer stem cell-like activity in colorectal carcinoma [27], and Tanabe et al. reported that YTHDC2 was upregulated in colon cancer and had a positive correlation with tumor stages [28]. Although YTHDF2, YTHDF3, and YTHDC1 showed essential roles in multiple cancer types [29–32], to date, no research on these regulators in COAD has been conducted. Therefore, the role of YTHDF2, YTHDF3, and YTHDC1 in COAD needs to be further studied. Our study showed a negative relationship between METTL14 and clinical stage, which implied its critical role in COAD progression. Ma et al. reported that METTL14 inhibits the metastatic potential of hepatocellular carcinoma by modulating N6-methyladenosine-dependent primary microRNA processing [33]. Further research is needed to explore the function of METTL14.

Moreover, our study showed a high correlation between the expression of YTHDF3 and KIAA1429 in COAD. We also observed a moderate correlation between METTL14 and YTHDF2, YTHDC1, and YTHDC2. The PPI network showed the interactions among "writers", "readers", and "erasers". The cross-talk among different categories of m⁶A regulators may influence cancer growth and progression. Chen et al. found that METTL3 promoted liver cancer progression through YTHDF2-dependent posttranscriptional silencing of SOCS2 [34]. Panneerdoss et al. reported that METTL14 and ALKBH5 inhibited the expression of YTHDF3, reversely block RNA demethylase activity, and altered the m⁶A status of target transcripts in cancer cells [10]. These studies have emphasized interactions between writers, readers, and erasers. Moreover, the interactions of members in the same category are also frequent. For example, YTHDF3 initiates mRNA translation and methylated mRNA decay through cooperation with YTHDF1 and YTHDF2, affecting the functions of the other two YTHDFs [25]. Therefore, the interactions of these regulators may play essential roles in COAD and should be further explored.

GSEA revealed that YTHDF1, YTHDF3, and YTHDC2 were enriched in several meaningful pathways. YTHDF3 and YTHDC2 share the same pathways of ubiquitin-mediated proteolysis, which further illustrates their functional biological connection. Taniue et al. found that lncRNA UPAT and UHRF1 may be promising molecular targets for the therapy of colon cancer by regulating protein ubiquitination and degradation and thereby play a critical role in the survival and tumorigenicity of cancer cells [35]. We suggest that the ubiquitin-mediated proteolysis affected by YTHDF3 and YTHDC2 may play a crucial role in tumor progression. The spliceosome can be induced for the activation of splicing and mRNA production in the carcinogenic process. Takayama et al. suggested that targeting spliceosome proteins by RNA-binding protein to promote AR splicing and expression could be a therapeutic possibility for hormone-refractory prostate cancer [36]. We hypothesize that YTHDF1 could also be a potential therapeutic target by modulating spliceosome and other RNA activities. TGF-β promotes tumor growth and metastasis by inducing angiogenic factors and facilitating EMT [37]. TGF-β signaling-associated genes are particularly sensitive to changes in m⁶A levels [10]; thus, the malfunction of the TGF-β signaling pathway in response to YTHDF3 dysregulation may be the main factor affecting the prognosis of COAD.

5. Conclusions

Most m⁶A-related proteins are dysregulated in COAD samples compared to normal samples, and some are associated with clinical features. Our results indicated a significant role of the YTH domain family ("readers") in the diagnosis, progression, and prognosis of COAD. The exact mechanism of the YTH domain family of N6-methyladenosine readers is worth further study.

Data Availability

All data generated or analyzed during this study are included in this published article.

Ethical Approval

This study was approved by the ethics committee of Nanjing Medical University.

All data were downloaded from the public database and followed the data access policy. All subjects were anonymous. So, there was no requirement for informed consent.

Disclosure

The funding agencies had no role in the study design, data collection, analysis, decision to publish, or preparation of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Authors’ Contributions

All authors contributed to data analysis and drafting or revising the article, gave final approval of the version to be published, and agreed to be accountable for all aspects of the work. Dian Xu, Jun Shao and Huan Song contributed equally to this work.

Acknowledgments

This study was funded by the National Natural Science Foundation of China (81673249), the National Key R&D Program of China (2017YFC0907000), the Qinglan Project of Jiangsu Province of China (2019), and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).

Supplementary Materials

Supplementary Figure S1: Pathways enriched according to GSEA of YTHDF1, YTHDF3, and YTHDC2. Supplementary Figure S2: PPI network of m⁶A RNA methylation regulators. (Supplementary Materials)

References

J. Thomas, M. Ohtsuka, M. Pichler, and H. Ling, “MicroRNAs: clinical relevance in colorectal cancer,” International Journal of Molecular Sciences, vol. 16, no. 12, pp. 28063–28076, 2015.
View at: Publisher Site | Google Scholar
R. L. Siegel, K. D. Miller, and A. Jemal, “Cancer statistics, 2016,” CA: a Cancer Journal for Clinicians, vol. 66, no. 1, pp. 7–30, 2016.
View at: Publisher Site | Google Scholar
Z. Miao, S. Jiang, M. Ding et al., “Ultrasmall rhodium nanozyme with RONS scavenging and photothermal activities for anti-inflammation and theranostics of colon diseases,” Nano Letters, vol. 20, no. 5, pp. 3079–3089, 2020.
View at: Publisher Site | Google Scholar
T. Sun, R. Wu, and L. Ming, “The role of m⁶A RNA methylation in cancer,” Biomedicine & Pharmacotherapy, vol. 112, p. 108613, 2019.
View at: Publisher Site | Google Scholar
S. R. Jaffrey and M. G. Kharas, “Emerging links between m⁶A and misregulated mRNA methylation in cancer,” Genome Medicine, vol. 9, no. 1, p. 2, 2017.
View at: Publisher Site | Google Scholar
J. Wan, W. Wu, Y. Che, N. Kang, and R. Zhang, “Insights into the potential use of microRNAs as a novel class of biomarkers in esophageal cancer,” Diseases of the Esophagus, vol. 29, no. 5, pp. 412–420, 2016.
View at: Publisher Site | Google Scholar
Z. Liang, R. L. Kidwell, H. Deng, and Q. Xie, “Epigenetic N6-methyladenosine modification of RNA and DNA regulates cancer,” Cancer Biology & Medicine, vol. 17, no. 1, pp. 9–19, 2020.
View at: Publisher Site | Google Scholar
N. J. Fry, B. A. Law, O. R. Ilkayeva, K. R. Carraway, C. L. Holley, and K. D. Mansfield, “N6-Methyladenosine contributes to cellular phenotype in a genetically-defined model of breast cancer progression,” Oncotarget, vol. 9, no. 58, pp. 31231–31243, 2018.
View at: Publisher Site | Google Scholar
J. Luo, H. Liu, S. Luan, C. He, and Z. Li, “Aberrant regulation of mRNA m⁶A modification in cancer development,” International Journal of Molecular Sciences, vol. 19, no. 9, p. 2515, 2018.
View at: Publisher Site | Google Scholar
S. Panneerdoss, V. K. Eedunuri, P. Yadav et al., “Cross-talk among writers, readers, and erasers of m6A regulates cancer growth and progression,” Science Advances, vol. 4, no. 10, p. eaar8263, 2018.
View at: Publisher Site | Google Scholar
X. Zhao, Y. Chen, Q. Mao et al., “Overexpression of YTHDF1 is associated with poor prognosis in patients with hepatocellular carcinoma,” Cancer Biomarkers, vol. 21, no. 4, pp. 859–868, 2018.
View at: Publisher Site | Google Scholar
C. Zhang, D. Samanta, H. Lu et al., “Hypoxia induces the breast cancer stem cell phenotype by HIF-dependent and ALKBH5-mediated m6A-demethylation of NANOG mRNA,” Proceedings of the National Academy of Sciences of the United States of America, vol. 113, no. 14, pp. E2047–E2056, 2016.
View at: Publisher Site | Google Scholar
N. A. Abdul Aziz, N. M. Mokhtar, R. Harun et al., “A 19-Gene expression signature as a predictor of survival in colorectal cancer,” BMC Medical Genomics, vol. 9, no. 1, p. 58, 2016.
View at: Publisher Site | Google Scholar
A. Blum, P. Wang, and J. C. Zenklusen, “SnapShot: TCGA-analyzed tumors,” Cell, vol. 173, no. 2, p. 530, 2018.
View at: Publisher Site | Google Scholar
A. Subramanian, P. Tamayo, V. K. Mootha et al., “Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 43, pp. 15545–15550, 2005.
View at: Publisher Site | Google Scholar
B. A. Weinberg, J. L. Marshall, and M. E. Salem, “The growing challenge of young adults with colorectal cancer,” Oncology (Williston Park), vol. 31, no. 5, pp. 381–389, 2017.
View at: Google Scholar
S. Wang, Q. Wang, X. Zhang et al., “Distinct prognostic value of dynactin subunit 4 (DCTN4) and diagnostic value of DCTN1, DCTN2, and DCTN4 in colon adenocarcinoma,” Cancer Management and Research, vol. Volume 10, pp. 5807–5824, 2018.
View at: Publisher Site | Google Scholar
J. H. Pan, H. Zhou, L. Cooper et al., “LAYN is a prognostic biomarker and correlated with immune infiltrates in gastric and colon cancers,” Frontiers in Immunology, vol. 10, p. 6, 2019.
View at: Publisher Site | Google Scholar
K. Zhang, J. Yan, B. Yi, Y. Rui, and H. Hu, “High KCNQ1OT1 expression might independently predict shorter survival of colon adenocarcinoma,” Future Oncology, vol. 15, no. 10, pp. 1085–1095, 2019.
View at: Publisher Site | Google Scholar
S. Liu, L. Chen, and Y. Xu, “Significance of PYK2 level as a prognosis predictor in patients with colon adenocarcinoma after surgical resection,” Onco Targets Ther, vol. Volume 11, pp. 7625–7634, 2018.
View at: Publisher Site | Google Scholar
X. Wang, Z. Lu, A. Gomez et al., “N6-Methyladenosine-dependent regulation of messenger RNA stability,” Nature, vol. 505, no. 7481, pp. 117–120, 2014.
View at: Publisher Site | Google Scholar
C. Xu, X. Wang, K. Liu et al., “Structural basis for selective binding of m⁶A RNA by the YTHDC1 YTH domain,” Nature Chemical Biology, vol. 10, no. 11, pp. 927–929, 2014.
View at: Publisher Site | Google Scholar
X. Wang, B. S. Zhao, I. A. Roundtree et al., “N(6)-Methyladenosine modulates messenger RNA translation efficiency,” Cell, vol. 161, no. 6, pp. 1388–1399, 2015.
View at: Publisher Site | Google Scholar
A. S. Bailey, P. J. Batista, R. S. Gold et al., “The conserved RNA helicase YTHDC2 regulates the transition from proliferation to differentiation in the germline,” eLife, vol. 6, 2017.
View at: Publisher Site | Google Scholar
H. Shi, X. Wang, Z. Lu et al., “YTHDF3 facilitates translation and decay of N6-methyladenosine-modified RNA,” Cell Research, vol. 27, no. 3, pp. 315–328, 2017.
View at: Publisher Site | Google Scholar
A. Li, Y. S. Chen, X. L. Ping et al., “Cytoplasmic m⁶A reader YTHDF3 promotes mRNA translation,” Cell Research, vol. 27, no. 3, pp. 444–447, 2017.
View at: Publisher Site | Google Scholar
Y. Bai, C. Yang, R. Wu et al., “YTHDF1 regulates tumorigenicity and cancer stem cell-like activity in human colorectal carcinoma,” Frontiers in Oncology, vol. 9, p. 332, 2019.
View at: Publisher Site | Google Scholar
A. Tanabe, K. Tanikawa, M. Tsunetomi et al., “RNA helicase YTHDC2 promotes cancer metastasis via the enhancement of the efficiency by which HIF-1α mRNA is translated,” Cancer Letters, vol. 376, no. 1, pp. 34–42, 2016.
View at: Publisher Site | Google Scholar
J. Chen, Y. Sun, X. Xu et al., “YTH domain family 2 orchestrates epithelial-mesenchymal transition/proliferation dichotomy in pancreatic cancer cells,” Cell Cycle, vol. 16, no. 23, pp. 2259–2271, 2017.
View at: Publisher Site | Google Scholar
H. Sheng, Z. Li, S. Su et al., “YTH domain family 2 promotes lung cancer cell growth by facilitating 6-phosphogluconate dehydrogenase mRNA translation,” Carcinogenesis, vol. 2019, 2019.
View at: Publisher Site | Google Scholar
Z. Zhao, J. Meng, R. Su et al., “Epitranscriptomics in liver disease: basic concepts and therapeutic potential,” Journal of Hepatology, vol. 2020, 2020.
View at: Publisher Site | Google Scholar
L. Liu, X. Liu, Z. Dong et al., “N6-Methyladenosine-related genomic targets are altered in breast cancer tissue and associated with poor survival,” Journal of Cancer, vol. 10, no. 22, pp. 5447–5459, 2019.
View at: Publisher Site | Google Scholar
J. Z. Ma, F. Yang, C. C. Zhou et al., “METTL14 suppresses the metastatic potential of hepatocellular carcinoma by modulating N(6)-methyladenosine-dependent primary microRNA processing,” Hepatology, vol. 65, no. 2, pp. 529–543, 2016.
View at: Google Scholar
M. Chen, L. Wei, C. T. Law et al., “RNA N6-methyladenosine methyltransferase-like 3 promotes liver cancer progression through YTHDF2-dependent posttranscriptional silencing of SOCS2,” Hepatology, vol. 67, no. 6, pp. 2254–2270, 2018.
View at: Publisher Site | Google Scholar
K. Taniue, A. Kurimoto, H. Sugimasa et al., “Long noncoding RNAUPAT promotes colon tumorigenesis by inhibiting degradation of UHRF1,” Proceedings of the National Academy of Sciences of the United States of America, vol. 113, no. 5, pp. 1273–1278, 2016.
View at: Publisher Site | Google Scholar
K. I. Takayama, T. Suzuki, T. Fujimura et al., “Dysregulation of spliceosome gene expression in advanced prostate cancer by RNA-binding protein PSF,” Proceedings of the National Academy of Sciences of the United States of America, vol. 114, no. 39, pp. 10461–10466, 2017.
View at: Publisher Site | Google Scholar
S. Colak and P. Ten Dijke, “Targeting TGF-β Signaling in Cancer,” Trends Cancer, vol. 3, no. 1, pp. 56–71, 2017.
View at: Publisher Site | Google Scholar

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Copyright © 2020 Dian Xu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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BioMed Research International

The YTH Domain Family of N6-Methyladenosine “Readers” in the Diagnosis and Prognosis of Colonic Adenocarcinoma

Abstract

1. Introduction

2. Materials and Methods

2.1. Data Processing

2.2. Portraying the Landscape of m6A RNA Methylation Regulator Expression

2.3. Survival Analysis

2.4. Biological Function Analysis

2.5. Statistical Analysis

3. Results

3.1. The Landscape of m6A RNA Methylation Regulators in COAD

3.2. m6A RNA Methylation Regulators and Clinicopathological Features

3.3. Prognostic Value of m6A RNA Methylation Regulators

3.4. Nomogram to Predict the Survival of COAD

3.5. GSEA Identified Related Signaling Pathways

3.6. PPI Network Construction

4. Discussion

5. Conclusions

Data Availability

Ethical Approval

Consent

Disclosure

Conflicts of Interest

Authors’ Contributions

Acknowledgments

Supplementary Materials

References

Copyright

2.2. Portraying the Landscape of m⁶A RNA Methylation Regulator Expression

3.1. The Landscape of m⁶A RNA Methylation Regulators in COAD

3.2. m⁶A RNA Methylation Regulators and Clinicopathological Features

3.3. Prognostic Value of m⁶A RNA Methylation Regulators