Evidence map›Paper›PMID 37877615›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Ac4C Enhances the Translation Efficiency of Vegfa mRNA and Mediates Central Sensitization in Spinal Dorsal Horn in Neuropathic Pain.

Ting Xu, Jing Wang, Yan Wu, Jia-Yan Wu, Wei-Cheng Lu, Meng Liu, Su-Bo Zhang, Dan Xie, Wen-Jun Xin, Jing-Dun Xie

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 30 citations in OpenAlex.

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  19. Loss of NAT10 Reduces the Translation ofJournal of the American Heart Association · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Ting XuNeuroscience Program, Zhongshan School of Medicine, The Fifth Affiliated Hospital, Guangdong Province Key Laboratory of Brain Function and Disease, Department of Physiology and Pain Research Center, Sun Yat-Sen University, Guangzhou, 510080, China.
Jing WangNeuroscience Program, Zhongshan School of Medicine, The Fifth Affiliated Hospital, Guangdong Province Key Laboratory of Brain Function and Disease, Department of Physiology and Pain Research Center, Sun Yat-Sen University, Guangzhou, 510080, China.
Yan WuDepartment of Anesthesiology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, 510062, China.
Jia-Yan WuNeuroscience Program, Zhongshan School of Medicine, The Fifth Affiliated Hospital, Guangdong Province Key Laboratory of Brain Function and Disease, Department of Physiology and Pain Research Center, Sun Yat-Sen University, Guangzhou, 510080, China.
Wei-Cheng LuState Key Laboratory of Oncology in Southern China, Collaborative Innovation for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Meng LiuDepartment of Anesthesia and Pain Medicine, Guangzhou First People's Hospital, Guangzhou, 510180, China.
Su-Bo ZhangState Key Laboratory of Oncology in Southern China, Collaborative Innovation for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Dan XieState Key Laboratory of Oncology in Southern China, Collaborative Innovation for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Wen-Jun XinNeuroscience Program, Zhongshan School of Medicine, The Fifth Affiliated Hospital, Guangdong Province Key Laboratory of Brain Function and Disease, Department of Physiology and Pain Research Center, Sun Yat-Sen University, Guangzhou, 510080, China.
Jing-Dun XieState Key Laboratory of Oncology in Southern China, Collaborative Innovation for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.ORCID 0000-0002-3820-8435
Sun Yat-sen University · CNGuangzhou First People's Hospital · CN

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2019B151502010Basic and Applied Basic Research Foundation of Guangdong Province 2022A1515012259Basic and Applied Basic Research Foundation of Guangdong Province 2023A1515030020China Postdoctoral Science Foundation 2022M723652Guangzhou Science and Technology Plan Project 202201010988Guangzhou Science and Technology Plan Project 20226060004National Key R&D Program of China 2021YFA1300201National Natural Science Foundation of China 31970936National Natural Science Foundation of China 81870878National Natural Science Foundation of China 82201373National Natural Science Foundation of China 82201377
6 · The paper itself

Abstract

N4-Acetylcytidine (ac4C), a highly conserved post-transcriptional machinery with extensive existence for RNA modification, plays versatile roles in various cellular processes and functions. However, the molecular mechanism by which ac4C modification mediates neuropathic pain remains elusive. Here, it is found that the enhanced ac4C modification promotes the recruitment of polysome in Vegfa mRNA and strengthens the translation efficiency following SNI. Nerve injury increases the expression of NAT10 and the interaction between NAT10 and Vegfa mRNA in the dorsal horn neurons, and the gain and loss of NAT10 function further confirm that NAT10 is involved in the ac4C modification in Vegfa mRNA and pain behavior. Moreover, the ac4C-mediated VEGFA upregulation contributes to the central sensitivity and neuropathic pain induced by SNI or AAV-hSyn-NAT10. Finally, SNI promotes the binding of HNRNPK in Vegfa mRNA and subsequently recruits the NAT10. The enhanced interaction between HNRNPK and NAT10 contributes to the ac4C modification of Vegfa mRNA and neuropathic pain. These findings suggest that the enhanced interaction between HNRNPK and Vegfa mRNA upregulates the ac4C level by recruiting NAT10 and contributes to the central sensitivity and neuropathic pain following SNI. Blocking this cascade may be a novel therapeutic approach in patients with neuropathic pain.

Indexed as

Central Nervous System SensitizationNeuralgiaHumansRNA, MessengerSpinal Cord Dorsal HornUp-RegulationRNA, Messengerac4C modificationNAT10neuropathic painspinal dorsal horntranslation efficiencyVEGFA

Identifiers

PMID37877615
PMCPMC10724395
OpenAlexW4387931525

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.