Role, mechanism, and application of N6-methyladenosine in hepatobiliary carcinoma

被引:0
作者
Jia, Chen [1 ]
Lang, Qing-Fu [1 ]
Yin, Zhi-Jie [1 ]
Sun, Jia [1 ]
Meng, Qing-Hui [1 ]
Pei, Tie-Min [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Gen Surg, 23 Postal St, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatobiliary carcinoma; RNA modification; N6-methyladenosine; Therapeutic targets; Treatment; MESSENGER-RNA TRANSLATION; HEPATOCELLULAR-CARCINOMA; CANCER PROGRESSION; M(6)A MODIFICATION; DEMETHYLASE; METHYLATION; METTL14; PROTEIN; SUPPRESSES;
D O I
10.4251/wjgo.v17.i6.105140
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatobiliary carcinoma is a frequently occurring and highly invasive cancer within the digestive tract, known for its rapid progression. Due to its difficult diagnosis and treatment in clinical practice, hepatobiliary carcinoma is a serious threat to human life and health. In recent years, the incidence of hepatobiliary carcinoma has gradually increased. N6-methyladenosine (m6A) modification, as a reversible post-transcriptional modification of the adenosine N6 site, is one of the most important RNA modifications in eukaryotes. Emerging research indicates that m6A affects the biological process of cells through the regulation of gene expression. m6A modification also plays a key role in the occurrence and development of various cancers. This review summarizes the role and mechanism of m6A modification in hepatobiliary carcinoma, and discussed its potential clinical application, so as to provide a theoretical reference for the individualized treatment of hepatobiliary carcinoma.
引用
收藏
页数:16
相关论文
共 133 条
[1]   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
[2]   The molecular hallmarks of epigenetic control [J].
Allis, C. David ;
Jenuwein, Thomas .
NATURE REVIEWS GENETICS, 2016, 17 (08) :487-500
[3]   YTHDF2 promotes gallbladder cancer progression and gemcitabine resistance via m6A-dependent DAPK3 degradation [J].
Bai, Xuesong ;
Chen, Jiemin ;
Zhang, Wenqin ;
Zhou, Shengnan ;
Dong, Liangbo ;
Huang, Jianhao ;
He, Xiaodong .
CANCER SCIENCE, 2023, 114 (11) :4299-4313
[4]   Cholangiocarcinoma 2020: the next horizon in mechanisms and management [J].
Banales, Jesus M. ;
Marin, Jose J. G. ;
Lamarca, Angela ;
Rodrigues, Pedro M. ;
Khan, Shahid A. ;
Roberts, Lewis R. ;
Cardinale, Vincenzo ;
Carpino, Guido ;
Andersen, Jesper B. ;
Braconi, Chiara ;
Calvisi, Diego F. ;
Perugorria, Maria J. ;
Fabris, Luca ;
Boulter, Luke ;
Macias, Rocio I. R. ;
Gaudio, Eugenio ;
Alvaro, Domenico ;
Gradilone, Sergio A. ;
Strazzabosco, Mario ;
Marzioni, Marco ;
Coulouarn, Cedric ;
Fouassier, Laura ;
Raggi, Chiara ;
Invernizzi, Pietro ;
Mertens, Joachim C. ;
Moncsek, Anja ;
Rizvi, Sumera ;
Heimbach, Julie ;
Koerkamp, Bas Groot ;
Bruix, Jordi ;
Forner, Alejandro ;
Bridgewater, John ;
Valle, Juan W. ;
Gores, Gregory J. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2020, 17 (09) :557-588
[5]   N6-methyladenosine demethylase FTO targets pre-mRNAs and regulates alternative splicing and 3'-end processing [J].
Bartosovic, Marek ;
Molares, Helena Covelo ;
Gregorova, Pavlina ;
Hrossova, Dominika ;
Kudla, Grzegorz ;
Vanacova, Stepanka .
NUCLEIC ACIDS RESEARCH, 2017, 45 (19) :11356-11370
[6]  
BOKAR JA, 1994, J BIOL CHEM, V269, P17697
[7]   METTL3 promotes glycolysis and cholangiocarcinoma progression by mediating the m6A modification of AKR1B10 [J].
Cai, Jingli ;
Cui, Zheng ;
Zhou, Jingyi ;
Zhang, Bosen ;
Lu, Ruiqi ;
Ding, Youcheng ;
Hu, Hai .
CANCER CELL INTERNATIONAL, 2022, 22 (01)
[8]   Development of Cell-Active N6-Methyladenosine RNA Demethylase FTO Inhibitor [J].
Chen, Baoen ;
Ye, Fei ;
Yu, Lu ;
Jia, Guifang ;
Huang, Xiaotian ;
Zhang, Xueju ;
Peng, Shuying ;
Chen, Kai ;
Wang, Meining ;
Gong, Shouze ;
Zhang, Ruihan ;
Yin, Jinya ;
Li, Haiyan ;
Yang, Yiming ;
Liu, Hong ;
Zhang, Jiwen ;
Zhang, Haiyan ;
Zhang, Ao ;
Jiang, Hualiang ;
Luo, Cheng ;
Yang, Cai-Guang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (43) :17963-17971
[9]   METTL3-mediated N6-methyladenosine modification of DUSP5 mRNA promotes gallbladder-cancer progression [J].
Chen, Hua-Dong ;
Li, Fuxi ;
Chen, Siyun ;
Zhong, Zhi-Hai ;
Gao, Peng-Fei ;
Gao, Wen-Zong .
CANCER GENE THERAPY, 2022, 29 (07) :1012-1020
[10]   YTH domain family 2 orchestrates epithelial-mesenchymal transition/proliferation dichotomy in pancreatic cancer cells [J].
Chen, Jixiang ;
Sun, Yaocheng ;
Xu, Xiao ;
Wang, Dawei ;
He, Junbo ;
Zhou, Hailang ;
Lu, Ying ;
Zeng, Jian ;
Du, Fengyi ;
Gong, Aihua ;
Xu, Min .
CELL CYCLE, 2017, 16 (23) :2259-2271