Open Access
Open access
volume 12 issue 5 pages 2193-2205

Detailed resume of RNA m6A demethylases

Dan-Dan Shen 1, 2, 3, 4, 5, 6
Bo Wang 1, 2, 3, 4, 5, 6
J Tian 1, 2, 3, 4, 5, 6
Lijuan Zhao 1, 2, 3, 4, 5, 6
Yaping Bi 1, 2, 3, 4, 5, 6
Jinge Zhang 1, 2, 3, 4, 5, 6
Ning Wang 7
Huiqin Kang 1, 2, 3, 4, 5, 6
Jingru Pang 1, 2, 3, 4, 5, 6
Ying Liu 1, 2, 3, 4, 5, 6
Luping Pang 1, 2, 3, 4, 5, 6
Zhe-Sheng Chen 8
Yichao Zheng 1, 2, 3, 4, 5, 6
Hongmin Liu 1, 2, 3, 4, 5, 6
1
 
Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education of China
2
 
Collaborative Innovation Center of New Drug Research and Safety Evaluation, Henan Province
3
 
Key Laboratory of Henan Province for Drug Quality and Evaluation
4
 
Institute of Drug Discovery and Development
5
 
School of Pharmaceutical Sciences
8
 
Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA
Publication typeJournal Article
Publication date2022-05-01
scimago Q1
wos Q1
SJR3.489
CiteScore24.3
Impact factor14.6
ISSN22113835, 22113843
General Pharmacology, Toxicology and Pharmaceutics
Abstract
N 6-Methyladenosine (m 6 A) is the most abundant internal modification in eukaryotic mRNA, playing critical role in various bioprocesses. Like other epigenetic modifications, m 6 A modification can be catalyzed by the methyltransferase complex and erased dynamically to maintain cells homeostasis. Up to now, only two m 6 A demethylases have been reported, fat mass and obesity-associated protein (FTO) and alkylation protein AlkB homolog 5 (ALKBH5), involving in a wide range of mRNA biological progress, including mRNA shearing, export, metabolism and stability. Furthermore, they participate in many significantly biological signaling pathway, and contribute to the progress and development of cancer along with other diseases. In this review, we focus on the studies about structure, inhibitors development and biological function of FTO and ALKBH5. This review systematically describes the chemical and biological functions of RNA demethylases FTO and ALKBH5, from their crystal structure to inhibitors development and screening, demethylation mechanism and substrates to biological functions and roles in diseases.
Found 
Found 

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GOST |
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GOST Copy
Shen D. et al. Detailed resume of RNA m6A demethylases // Acta Pharmaceutica Sinica B. 2022. Vol. 12. No. 5. pp. 2193-2205.
GOST all authors (up to 50) Copy
Shen D. et al. Detailed resume of RNA m6A demethylases // Acta Pharmaceutica Sinica B. 2022. Vol. 12. No. 5. pp. 2193-2205.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.apsb.2022.01.003
UR - https://doi.org/10.1016/j.apsb.2022.01.003
TI - Detailed resume of RNA m6A demethylases
T2 - Acta Pharmaceutica Sinica B
AU - Shen, Dan-Dan
AU - Wang, Bo
AU - Tian, J
AU - Zhao, Lijuan
AU - Bi, Yaping
AU - Zhang, Jinge
AU - Wang, Ning
AU - Kang, Huiqin
AU - Pang, Jingru
AU - Liu, Ying
AU - Pang, Luping
AU - Chen, Zhe-Sheng
AU - Zheng, Yichao
AU - Liu, Hongmin
PY - 2022
DA - 2022/05/01
PB - Elsevier
SP - 2193-2205
IS - 5
VL - 12
PMID - 35646549
SN - 2211-3835
SN - 2211-3843
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2022_Shen,
author = {Dan-Dan Shen and Bo Wang and J Tian and Lijuan Zhao and Yaping Bi and Jinge Zhang and Ning Wang and Huiqin Kang and Jingru Pang and Ying Liu and Luping Pang and Zhe-Sheng Chen and Yichao Zheng and Hongmin Liu and others},
title = {Detailed resume of RNA m6A demethylases},
journal = {Acta Pharmaceutica Sinica B},
year = {2022},
volume = {12},
publisher = {Elsevier},
month = {may},
url = {https://doi.org/10.1016/j.apsb.2022.01.003},
number = {5},
pages = {2193--2205},
doi = {10.1016/j.apsb.2022.01.003}
}
MLA
Cite this
MLA Copy
Shen, Dan-Dan, et al. “Detailed resume of RNA m6A demethylases.” Acta Pharmaceutica Sinica B, vol. 12, no. 5, May. 2022, pp. 2193-2205. https://doi.org/10.1016/j.apsb.2022.01.003.
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