The Role of m6A Modification and m6A Regulators in Esophageal Cancer

被引:6
作者
Li, Yuekao [1 ]
Niu, Chaoxu [2 ]
Wang, Na [3 ]
Huang, Xi [3 ]
Cao, Shiru [3 ]
Cui, Saijin [3 ]
Chen, Tianyu [3 ]
Huo, Xiangran [3 ]
Zhou, Rongmiao [3 ]
机构
[1] Hebei Med Univ, Dept Computed Tomog, Hosp 4, Shijiazhuang 050011, Hebei, Peoples R China
[2] Shijiazhuang Pingan Hosp, Dept Surg, Shijiazhuang 050021, Hebei, Peoples R China
[3] Hebei Med Univ, Hebei Prov Canc Inst, Hosp 4, Shijiazhuang 050011, Hebei, Peoples R China
关键词
m(6)A modification; m(6)A regulators; occurrence; progression; treatment; prognosis; esophageal cancer; SQUAMOUS-CELL CARCINOMA; GENOME-WIDE ASSOCIATION; EUKARYOTIC TRANSLATION INITIATION; RNA-BINDING PROTEIN-3; MESSENGER-RNA; POOR-PROGNOSIS; N-6-METHYLADENOSINE MODIFICATION; SUSCEPTIBILITY LOCI; UP-REGULATION; NUCLEAR-RNA;
D O I
10.3390/cancers14205139
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary N-6-methyladenosine (m(6)A) modification and m(6)A regulators play important roles in the occurrence and development of various cancers. Esophageal cancer (ESCA), one of the most common gastrointestinal tumors, seriously affects people's health. In this review article, we summarized the role and possible mechanism of m(6)A modification and m(6)A regulators in the occurrence, progression, remedy and prognosis of ESCA, which might be useful for determining the pathogenesis of ESCA and providing direction for the future research of ESCA. N-6-methyladenosine (m(6)A) modification, the most prevalent RNA modification, is involved in all aspects of RNA metabolism, including RNA processing, nuclear export, stability, translation and degradation. Therefore, m(6)A modification can participate in various physiological functions, such as tissue development, heat shock response, DNA damage response, circadian clock control and even in carcinogenesis through regulating the expression or structure of the gene. The deposition, removal and recognition of m(6)A are carried out by methyltransferases, demethylases and m(6)A RNA binding proteins, respectively. Aberrant m(6)A modification and the dysregulation of m(6)A regulators play critical roles in the occurrence and development of various cancers. The pathogenesis of esophageal cancer (ESCA) remains unclear and the five-year survival rate of advanced ESCA patients is still dismal. Here, we systematically reviewed the recent studies of m(6)A modification and m(6)A regulators in ESCA and comprehensively analyzed the role and possible mechanism of m(6)A modification and m(6)A regulators in the occurrence, progression, remedy and prognosis of ESCA. Defining the effect of m(6)A modification and m(6)A regulators in ESCA might be helpful for determining the pathogenesis of ESCA and providing some ideas for an early diagnosis, individualized treatment and improved prognosis of ESCA patients.
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页数:27
相关论文
共 177 条
[1]   Cap-specific terminal N6-methylation of RNA by an RNA polymerase II-associated methyltransferase [J].
Akichika, Shinichiro ;
Hirano, Seiichi ;
Shichino, Yuichi ;
Suzuki, Takeo ;
Nishimasu, Hiroshi ;
Ishitani, Ryuichiro ;
Sugita, Ai ;
Hirose, Yutaka ;
Iwasaki, Shintaro ;
Nureki, Osamu ;
Suzuki, Tsutomu .
SCIENCE, 2019, 363 (6423) :141-141
[2]   HNRNPA2B1 Is a Mediator of m6A-Dependent Nuclear RNA Processing Events [J].
Alarcon, Claudio R. ;
Goodarzi, Hani ;
Lee, Hyeseung ;
Liu, Xuhang ;
Tavazoie, Saeed ;
Tavazoie, Sohail F. .
CELL, 2015, 162 (06) :1299-1308
[3]   N6-methyladenosine marks primary microRNAs for processing [J].
Alarcon, Claudio R. ;
Lee, Hyeseung ;
Goodarzi, Hani ;
Halberg, Nils ;
Tavazoie, Sohail F. .
NATURE, 2015, 519 (7544) :482-+
[4]   The role of m6A RNA methylation in cancer metabolism [J].
An, Yuanyuan ;
Duan, Hua .
MOLECULAR CANCER, 2022, 21 (01)
[5]   Tumor immune microenvironment and immune checkpoint inhibitors in esophageal squamous cell carcinoma [J].
Baba, Yoshifumi ;
Nomoto, Daichi ;
Okadome, Kazuo ;
Ishimoto, Takatsugu ;
Iwatsuki, Masaaki ;
Miyamoto, Yuji ;
Yoshida, Naoya ;
Baba, Hideo .
CANCER SCIENCE, 2020, 111 (09) :3132-3141
[6]   Loss of YTHDF1 in gastric tumors restores sensitivity to antitumor immunity by recruiting mature dendritic cells [J].
Bai, Xiaowu ;
Wong, Chi Chun ;
Pan, Yasi ;
Chen, Huarong ;
Liu, Weixin ;
Zhai, Jianning ;
Kang, Wei ;
Shi, Yu ;
Yamamoto, Masami ;
Tsukamoto, Tetsuya ;
Nomura, Sachiyo ;
Chiu, Philip ;
Yu, Jun ;
Kwok-wai Ng, Enders .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2022, 10 (02)
[7]   LOCALIZATION OF N6-METHYLADENOSINE IN ROUS-SARCOMA VIRUS GENOME [J].
BEEMON, K ;
KEITH, J .
JOURNAL OF MOLECULAR BIOLOGY, 1977, 113 (01) :165-179
[8]   MODOMICS: a database of RNA modification pathways. 2017 update [J].
Boccaletto, Pietro ;
Machnicka, Magdalena A. ;
Purta, Elzbieta ;
Piatkowski, Pawe ;
Baginski, Blazej ;
Wirecki, Tomasz K. ;
de Crecy-Lagard, Valerie ;
Ross, Robert ;
Limbach, Patrick A. ;
Kotter, Annika ;
Helm, Mark ;
Bujnicki, Janusz M. .
NUCLEIC ACIDS RESEARCH, 2018, 46 (D1) :D303-D307
[9]  
Bokar JA, 1997, RNA, V3, P1233
[10]   IMP3 overexpression occurs in various important cancer types and is linked to aggressive tumor features: A tissue microarray study on 8,877 human cancers and normal tissues [J].
Burdelski, Christoph ;
Jakani-Karimi, Nilofar ;
Jacobsen, Frank ;
Moeller-Koop, Christina ;
Miner, Sarah ;
Simon, Ronald ;
Sauter, Guido ;
Steurer, Stefan ;
Clauditz, Til S. ;
Wilczak, Waldemar .
ONCOLOGY REPORTS, 2018, 39 (01) :3-12