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Published on: February 27, 2016
Research progress on NAT10-mediated acetylation in normal development and disease
Da Qin1, Qing Liu1, Xiaochao Ma1
1Department of Thoracic Surgery II, Organ Transplantation Center, The First Hospital of Jilin University, Changchun, China.
N4-acetylcytidine (ac4C) is an RNA modification impacting RNA stability and translation. NAT10 enzyme-mediated ac4C is crucial in physiological processes and cancer, offering therapeutic potential.
Area of Science:
- Molecular Biology
- Epigenetics
- Biochemistry
Background:
- N4-acetylcytidine (ac4C) is an evolutionarily conserved RNA modification.
- This modification is catalyzed by the acetyltransferase NAT10, a dual-function enzyme.
- ac4C regulates RNA stability, translation, and various post-transcriptional processes.
Purpose of the Study:
- To review the structural and functional roles of NAT10-mediated acetylation.
- To explore the involvement of NAT10 in physiological contexts and cancer.
- To highlight emerging therapeutic opportunities targeting NAT10 and ac4C.
Main Methods:
- Literature review of structural and functional studies on NAT10.
- Analysis of NAT10's roles in cell division, differentiation, inflammation, aging, and viral infection.
- Examination of NAT10's oncogenic mechanisms and interactions with non-coding RNAs.
Main Results:
- NAT10-mediated acetylation plays significant roles in physiological processes.
- In cancer, NAT10 drives tumor progression via enhanced mRNA stability, cell cycle regulation, metastasis, and immune evasion.
- NAT10 also influences ferroptosis, metabolism, p53 activity, and drug resistance.
Conclusions:
- NAT10-mediated acetylation is a key regulator in both normal physiology and cancer.
- Targeting NAT10 and ac4C modifications presents promising therapeutic strategies.
- Future research should address microbiota-mediated ac4C regulation and the tumor immune microenvironment.
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