N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma

N6-methyladenosine (m6A) is the most abundant internal mRNA modification in eukaryotes and is related to stability, localization, or translation efficiency in tumorigenesis. Autophagy plays an important role in the occurrence and development of tumours. However, the relationship between m6A and auto...

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Autores principales: Fang Wang, Yue Zhu, Hongshi Cai, Jianfeng Liang, Wenjin Wang, Yan Liao, Yadong Zhang, Cheng Wang, Jinsong Hou
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:d7c55bd7205047558cec9685e836ad392021-11-30T19:15:49ZN6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma2234-943X10.3389/fonc.2021.738406https://doaj.org/article/d7c55bd7205047558cec9685e836ad392021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fonc.2021.738406/fullhttps://doaj.org/toc/2234-943XN6-methyladenosine (m6A) is the most abundant internal mRNA modification in eukaryotes and is related to stability, localization, or translation efficiency in tumorigenesis. Autophagy plays an important role in the occurrence and development of tumours. However, the relationship between m6A and autophagy remains unclear. In this study, we used a rapamycin-induced autophagy model of oral squamous cell carcinoma (OSCC) cells, and observed increased m6A RNA methylation. When autophagy was activated, the methyltransferase-like 14 (METTL14) expression was upregulated and influenced the proliferation, migration, and invasiveness of OSCC cells. Through meRIP-seq and RNA-seq analysis, we found that METTL14 directly combined with eukaryotic translation initiation factor gamma 1 (eIF4G1) mRNA and decreased its RNA stability. According to the dual-luciferase reporter and mutagenesis assay, the mutated site 1 of exon 11 of eIF4G1 is the key target of METTL14. Knockdown of the main m6A binding protein YTHDF2 may rescue the shortened half-life of eIF4G1 mRNA induced by METTL14 overexpression. Furthermore, an in vivo tumour xenograft model confirmed that a high METTL14 expression can effectively reduce OSCC growth. Additionally, using clinical samples, we found that patients with advanced or moderately/poorly differentiated tumours exhibited lower METTL14 levels. Taken together, our results revealed that METTL14 mediated eIF4G1 expression via m6A modification and regulated autophagy levels and biological functions in OSCC. Our findings not only expand our understanding of the correlation between autophagy and RNA methylation in tumorigenesis but also present an opportunity to develop new therapeutic options.Fang WangFang WangFang WangYue ZhuYue ZhuHongshi CaiHongshi CaiJianfeng LiangJianfeng LiangWenjin WangWenjin WangYan LiaoYan LiaoYadong ZhangYadong ZhangCheng WangCheng WangJinsong HouJinsong HouFrontiers Media S.A.articleoral squamous cell carcinomaautophagyRNA methylationtumorigenesismethyltransferase-like 14Neoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENFrontiers in Oncology, Vol 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic oral squamous cell carcinoma
autophagy
RNA methylation
tumorigenesis
methyltransferase-like 14
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle oral squamous cell carcinoma
autophagy
RNA methylation
tumorigenesis
methyltransferase-like 14
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Fang Wang
Fang Wang
Fang Wang
Yue Zhu
Yue Zhu
Hongshi Cai
Hongshi Cai
Jianfeng Liang
Jianfeng Liang
Wenjin Wang
Wenjin Wang
Yan Liao
Yan Liao
Yadong Zhang
Yadong Zhang
Cheng Wang
Cheng Wang
Jinsong Hou
Jinsong Hou
N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma
description N6-methyladenosine (m6A) is the most abundant internal mRNA modification in eukaryotes and is related to stability, localization, or translation efficiency in tumorigenesis. Autophagy plays an important role in the occurrence and development of tumours. However, the relationship between m6A and autophagy remains unclear. In this study, we used a rapamycin-induced autophagy model of oral squamous cell carcinoma (OSCC) cells, and observed increased m6A RNA methylation. When autophagy was activated, the methyltransferase-like 14 (METTL14) expression was upregulated and influenced the proliferation, migration, and invasiveness of OSCC cells. Through meRIP-seq and RNA-seq analysis, we found that METTL14 directly combined with eukaryotic translation initiation factor gamma 1 (eIF4G1) mRNA and decreased its RNA stability. According to the dual-luciferase reporter and mutagenesis assay, the mutated site 1 of exon 11 of eIF4G1 is the key target of METTL14. Knockdown of the main m6A binding protein YTHDF2 may rescue the shortened half-life of eIF4G1 mRNA induced by METTL14 overexpression. Furthermore, an in vivo tumour xenograft model confirmed that a high METTL14 expression can effectively reduce OSCC growth. Additionally, using clinical samples, we found that patients with advanced or moderately/poorly differentiated tumours exhibited lower METTL14 levels. Taken together, our results revealed that METTL14 mediated eIF4G1 expression via m6A modification and regulated autophagy levels and biological functions in OSCC. Our findings not only expand our understanding of the correlation between autophagy and RNA methylation in tumorigenesis but also present an opportunity to develop new therapeutic options.
format article
author Fang Wang
Fang Wang
Fang Wang
Yue Zhu
Yue Zhu
Hongshi Cai
Hongshi Cai
Jianfeng Liang
Jianfeng Liang
Wenjin Wang
Wenjin Wang
Yan Liao
Yan Liao
Yadong Zhang
Yadong Zhang
Cheng Wang
Cheng Wang
Jinsong Hou
Jinsong Hou
author_facet Fang Wang
Fang Wang
Fang Wang
Yue Zhu
Yue Zhu
Hongshi Cai
Hongshi Cai
Jianfeng Liang
Jianfeng Liang
Wenjin Wang
Wenjin Wang
Yan Liao
Yan Liao
Yadong Zhang
Yadong Zhang
Cheng Wang
Cheng Wang
Jinsong Hou
Jinsong Hou
author_sort Fang Wang
title N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma
title_short N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma
title_full N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma
title_fullStr N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma
title_full_unstemmed N6-Methyladenosine Methyltransferase METTL14-Mediated Autophagy in Malignant Development of Oral Squamous Cell Carcinoma
title_sort n6-methyladenosine methyltransferase mettl14-mediated autophagy in malignant development of oral squamous cell carcinoma
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/d7c55bd7205047558cec9685e836ad39
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